Item | Value |
---|---|
geneid | 5641 |
ensemblid | ENSG00000100600.15 |
hgncid | 9472 |
symbol | LGMN |
name | legumain |
refseq_nuc | NM_005606.7 |
refseq_prot | NP_005597.3 |
ensembl_nuc | ENST00000334869.9 |
ensembl_prot | ENSP00000334052.4 |
mane_status | MANE Select |
chr | chr14 |
start | 92703809 |
end | 92748627 |
strand | - |
ver | v1.2 |
region | chr14:92703809-92748627 |
region5000 | chr14:92698809-92753627 |
regionname0 | LGMN_chr14_92703809_92748627 |
regionname5000 | LGMN_chr14_92698809_92753627 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 433 | 322 | 61 | 57 | 148 | 17 | 37 | 115 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0002 | 0/0 | 433 | 87 | 34 | 20 | 29 | 1 | 3 | 20 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0003 | 0/0 | 433 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0004 | 0/0 | 433 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0005 | 0/0 | 433 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0006 | 0/0 | 433 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
a0007 | 0/0 | 433 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | MVWKV others(428): Show |
chr14 | 92698809 | 92753627 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1299 | 224 | 43 | 29 | 113 | 10 | 28 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0002 | 0/0 | 1299 | 63 | 11 | 20 | 16 | 7 | 9 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0004 | 0/0 | 1299 | 25 | 1 | 6 | 18 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0008 | 0/0 | 1299 | 3 | 3 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0012 | 0/0 | 1299 | 2 | 0 | 2 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0014 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0017 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0018 | 0/1 | 1299 | 1 | 0 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0001c0019 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0002c0003 | 0/0 | 1299 | 58 | 19 | 11 | 25 | 0 | 3 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0002c0005 | 0/0 | 1299 | 22 | 11 | 8 | 2 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0002c0006 | 0/0 | 1299 | 4 | 2 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0002c0009 | 0/0 | 1299 | 2 | 1 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0002c0015 | 0/0 | 1299 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0003c0007 | 0/0 | 1299 | 4 | 0 | 0 | 4 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0004c0013 | 0/0 | 1299 | 2 | 1 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0005c0010 | 0/0 | 1299 | 2 | 2 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0006c0011 | 0/0 | 1299 | 2 | 0 | 0 | 0 | 0 | 2 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 | ||
a0007c0016 | 0/0 | 1299 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | ATGGT others(1294): Show |
chr14 | 92698809 | 92753627 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1980 | 217 | 37 | 29 | 112 | 10 | 28 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0001t0002 | 0/0 | 1968 | 4 | 4 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1963): Show |
chr14 | 92698809 | 92753627 |
a0001c0001t0004 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1969): Show |
chr14 | 92698809 | 92753627 |
a0001c0001t0005 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0001t0007 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0002t0001 | 0/0 | 1980 | 60 | 8 | 20 | 16 | 7 | 9 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0002t0002 | 0/0 | 1968 | 3 | 3 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1963): Show |
chr14 | 92698809 | 92753627 |
a0001c0004t0001 | 0/0 | 1980 | 25 | 1 | 6 | 18 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0008t0001 | 0/0 | 1980 | 3 | 3 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0012t0001 | 0/0 | 1980 | 2 | 0 | 2 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0014t0001 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0017t0001 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0018t0001 | 0/1 | 1980 | 1 | 0 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0001c0019t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0003t0001 | 0/0 | 1980 | 51 | 12 | 11 | 25 | 0 | 3 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0003t0002 | 0/0 | 1968 | 4 | 4 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1963): Show |
chr14 | 92698809 | 92753627 |
a0002c0003t0004 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1969): Show |
chr14 | 92698809 | 92753627 |
a0002c0003t0005 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0003t0006 | 0/0 | 1974 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1969): Show |
chr14 | 92698809 | 92753627 |
a0002c0005t0001 | 0/0 | 1980 | 21 | 10 | 8 | 2 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0005t0008 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0006t0001 | 0/0 | 1980 | 4 | 2 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0009t0001 | 0/0 | 1980 | 2 | 1 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0002c0015t0003 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0003c0007t0001 | 0/0 | 1980 | 4 | 0 | 0 | 4 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0004c0013t0001 | 0/0 | 1980 | 2 | 1 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0005c0010t0003 | 0/0 | 1980 | 2 | 2 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0006c0011t0001 | 0/0 | 1980 | 2 | 0 | 0 | 0 | 0 | 2 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
a0007c0016t0001 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | AATCA others(1975): Show |
chr14 | 92698809 | 92753627 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0404 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0407 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0001g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0406 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0001g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0004t0001g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0008t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0008t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0008t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0012t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0012t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0014t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0014t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0017t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0018t0001g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0001c0019t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0001g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0003t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0001g0411 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0005t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0009t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0009t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0002c0015t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0003c0007t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0003c0007t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0003c0007t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0003c0007t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0004c0013t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0004c0013t0001g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0005c0010t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0005c0010t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0006c0011t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0006c0011t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
a0007c0016t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0005 | t0001 | g0411 | EUR | GBR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0161 | EUR | GBR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0282 | EUR | GBR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0391 | EUR | GBR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | FIN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00408 | hp1 | a0001 | c0004 | t0001 | g0325 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00423 | hp1 | a0001 | c0004 | t0001 | g0360 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00438 | hp2 | a0001 | c0004 | t0001 | g0252 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0335 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00609 | hp1 | a0001 | c0019 | t0001 | g0373 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0319 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0403 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00639 | hp1 | a0002 | c0005 | t0001 | g0012 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00639 | hp2 | a0002 | c0009 | t0001 | g0039 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0375 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0404 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0011 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0388 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0354 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0383 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG00741 | hp2 | a0002 | c0005 | t0001 | g0036 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0389 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0035 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0224 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01081 | hp1 | a0001 | c0004 | t0001 | g0381 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0008 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01099 | hp1 | a0004 | c0013 | t0001 | g0384 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01099 | hp2 | a0002 | c0005 | t0001 | g0037 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0228 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01109 | hp1 | a0002 | c0003 | t0001 | g0148 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0370 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01169 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0164 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0203 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0029 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0253 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01257 | hp2 | a0001 | c0012 | t0001 | g0160 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0378 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01258 | hp2 | a0001 | c0012 | t0001 | g0163 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0407 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0086 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0392 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0363 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01496 | hp1 | a0002 | c0005 | t0001 | g0220 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0374 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0199 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0344 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0274 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | IBS | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01884 | hp2 | a0002 | c0005 | t0001 | g0122 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01928 | hp2 | a0002 | c0005 | t0001 | g0200 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0225 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0379 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0326 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0330 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01975 | hp2 | a0002 | c0005 | t0001 | g0198 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01978 | hp1 | a0002 | c0005 | t0001 | g0236 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01978 | hp2 | a0001 | c0004 | t0001 | g0022 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0100 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02004 | hp1 | a0002 | c0005 | t0001 | g0201 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0400 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0159 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02055 | hp1 | a0002 | c0003 | t0001 | g0092 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02055 | hp2 | a0002 | c0006 | t0001 | g0150 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0398 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0393 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02074 | hp1 | a0003 | c0007 | t0001 | g0179 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0410 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02080 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0372 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02129 | hp2 | a0002 | c0005 | t0001 | g0260 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02132 | hp2 | a0003 | c0007 | t0001 | g0176 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02135 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02145 | hp2 | a0002 | c0005 | t0001 | g0099 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0069 | EAS | CDX | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | CDX | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02165 | hp1 | a0001 | c0004 | t0001 | g0309 | EAS | CDX | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0064 | EAS | CDX | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02258 | hp1 | a0002 | c0003 | t0002 | g0153 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02258 | hp2 | a0005 | c0010 | t0003 | g0093 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02273 | hp2 | a0001 | c0004 | t0001 | g0172 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0147 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0365 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0281 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02451 | hp2 | a0001 | c0008 | t0001 | g0044 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02523 | hp2 | a0002 | c0003 | t0001 | g0333 | EAS | KHV | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0368 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02572 | hp2 | a0002 | c0005 | t0001 | g0113 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02615 | hp1 | a0002 | c0015 | t0003 | g0041 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0409 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0149 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02717 | hp2 | a0002 | c0003 | t0005 | g0040 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02723 | hp1 | a0001 | c0014 | t0001 | g0047 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0385 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02818 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02886 | hp1 | a0002 | c0009 | t0001 | g0190 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02886 | hp2 | a0001 | c0008 | t0001 | g0043 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02922 | hp1 | a0001 | c0014 | t0001 | g0033 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02970 | hp2 | a0002 | c0003 | t0001 | g0191 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0109 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03041 | hp2 | a0002 | c0003 | t0006 | g0185 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03098 | hp1 | a0002 | c0006 | t0001 | g0267 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03130 | hp2 | a0005 | c0010 | t0003 | g0027 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03195 | hp1 | a0002 | c0005 | t0001 | g0184 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0008 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0367 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0120 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03453 | hp2 | a0002 | c0003 | t0001 | g0110 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0308 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0217 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0382 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03516 | hp1 | a0002 | c0005 | t0001 | g0030 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0361 | AFR | ESN | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03540 | hp2 | a0002 | c0005 | t0001 | g0348 | AFR | GWD | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0399 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03579 | hp2 | a0002 | c0003 | t0004 | g0146 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0278 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0380 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03688 | hp1 | a0006 | c0011 | t0001 | g0014 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0130 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0234 | SAS | PJL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0394 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03834 | hp1 | a0006 | c0011 | t0001 | g0013 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0123 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0401 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0402 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0405 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0355 | SAS | BEB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0362 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0406 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0049 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18522 | hp2 | a0002 | c0003 | t0002 | g0155 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | CHB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18942 | hp2 | a0001 | c0004 | t0001 | g0216 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18947 | hp2 | a0001 | c0004 | t0001 | g0339 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0295 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18953 | hp2 | a0003 | c0007 | t0001 | g0177 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18956 | hp1 | a0001 | c0004 | t0001 | g0353 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18965 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18967 | hp2 | a0001 | c0004 | t0001 | g0237 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18971 | hp1 | a0001 | c0004 | t0001 | g0084 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0065 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0292 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18985 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18988 | hp2 | a0002 | c0003 | t0001 | g0350 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18993 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18994 | hp1 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19011 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19030 | hp1 | a0002 | c0005 | t0001 | g0186 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19030 | hp2 | a0002 | c0003 | t0001 | g0334 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19043 | hp2 | a0002 | c0003 | t0002 | g0154 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19060 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19064 | hp2 | a0007 | c0016 | t0001 | g0323 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0396 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19075 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19075 | hp2 | a0001 | c0004 | t0001 | g0376 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19077 | hp1 | a0002 | c0006 | t0001 | g0080 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19077 | hp2 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19081 | hp1 | a0002 | c0005 | t0001 | g0387 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19081 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19083 | hp1 | a0002 | c0006 | t0001 | g0089 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0408 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19085 | hp2 | a0003 | c0007 | t0001 | g0178 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20129 | hp1 | a0001 | c0008 | t0001 | g0034 | AFR | ASW | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0285 | EUR | TSI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0071 | EUR | TSI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0386 | EUR | TSI | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0347 | SAS | GIH | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | GIH | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01123 | hp1 | a0002 | c0003 | t0001 | g0261 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02109 | hp1 | a0002 | c0005 | t0008 | g0192 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02109 | hp2 | a0002 | c0003 | t0002 | g0156 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02486 | hp1 | a0001 | c0017 | t0001 | g0095 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02559 | hp1 | a0002 | c0005 | t0001 | g0189 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03471 | hp1 | a0002 | c0005 | t0001 | g0112 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0307 | AFR | USA | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA20300 | hp2 | a0001 | c0004 | t0001 | g0171 | AFR | USA | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA21309 | hp1 | a0004 | c0013 | t0001 | g0162 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
homoSapiens | chm13v2 | a0001 | c0018 | t0001 | g0219 | REF | REF | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0270 | REF | REF | LGMN_chr14_92698809_92753627 | LGMN | chr14 | 92698809 | 92753627 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92709697 | G | A | 1 | a0004 | 2 | HG01099.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.995C>T | p.Thr332Met | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/14 | 1163/1980 | 995/1302 | 332/433 | chr14 | 92709697 | |||
chr14:92709812 | C | T | 1 | a0006 | 2 | HG03688.hp1 HG03834.hp1 |
missense_variant | MODERATE | c.880G>A | p.Val294Ile | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/14 | 1048/1980 | 880/1302 | 294/433 | chr14 | 92709812 | |||
chr14:92709823 | G | C | 1 | a0007 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.869C>G | p.Ala290Gly | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/14 | 1037/1980 | 869/1302 | 290/433 | chr14 | 92709823 | |||
chr14:92718769 | C | T | 1 | a0005 | 2 | HG02258.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.214G>A | p.Asp72Asn | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/14 | 382/1980 | 214/1302 | 72/433 | chr14 | 92718769 | |||
chr14:92718784 | C | T | 1 | a0003 | 4 | HG02074.hp1 HG02132.hp2 NA18953.hp2 others(1): Show |
missense_variant | MODERATE | c.199G>A | p.Val67Ile | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/14 | 367/1980 | 199/1302 | 67/433 | chr14 | 92718784 | |||
chr14:92732735 | C | T | 1 | a0002 | 87 | HG00099.hp1 HG00544.hp2 HG00639.hp1 others(84): Show |
missense_variant | MODERATE | c.52G>A | p.Val18Ile | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/14 | 220/1980 | 52/1302 | 18/433 | chr14 | 92732735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92704648 | C | T | 5 | a0001c0002 a0001c0012 a0001c0017 others(2): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
synonymous_variant | LOW | c.1251G>A | p.Pro417Pro | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/14 | 1419/1980 | 1251/1302 | 417/433 | chr14 | 92704648 | |||
chr14:92706558 | C | T | 1 | a0001c0012 | 2 | HG01257.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.1116G>A | p.Pro372Pro | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/14 | 1284/1980 | 1116/1302 | 372/433 | chr14 | 92706558 | |||
chr14:92706600 | C | T | 1 | a0002c0009 | 2 | HG00639.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.1074G>A | p.Ala358Ala | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/14 | 1242/1980 | 1074/1302 | 358/433 | chr14 | 92706600 | |||
chr14:92709774 | G | A | 1 | a0001c0008 | 3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.918C>T | p.Pro306Pro | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/14 | 1086/1980 | 918/1302 | 306/433 | chr14 | 92709774 | |||
chr14:92711713 | G | A | 2 | a0001c0014 a0002c0015 |
3 | HG02615.hp1 HG02723.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.765C>T | p.Tyr255Tyr | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/14 | 933/1980 | 765/1302 | 255/433 | chr14 | 92711713 | |||
chr14:92713880 | A | G | 1 | a0001c0017 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.486T>C | p.His162His | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/14 | 654/1980 | 486/1302 | 162/433 | chr14 | 92713880 | |||
chr14:92714382 | A | G | 4 | a0001c0004 a0002c0006 a0003c0007 others(1): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(31): Show |
synonymous_variant | LOW | c.474T>C | p.Asn158Asn | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/14 | 642/1980 | 474/1302 | 158/433 | chr14 | 92714382 | |||
chr14:92718770 | G | A | 1 | a0001c0019 | 1 | HG00609.hp1 | synonymous_variant | LOW | c.213C>T | p.Tyr71Tyr | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/14 | 381/1980 | 213/1302 | 71/433 | chr14 | 92718770 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92703813 | G | C | 1 | a0002c0003t0006 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 506 | chr14 | 92703813 | ||||||
chr14:92703953 | T | C | 1 | a0002c0005t0008 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 366 | chr14 | 92703953 | ||||||
chr14:92704032 | G | T | 2 | a0001c0001t0005 a0002c0003t0005 |
2 | HG02717.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*287C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 287 | chr14 | 92704032 | ||||||
chr14:92704069 | A | G | 1 | a0001c0001t0007 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 250 | chr14 | 92704069 | ||||||
chr14:92704181 | TCCTGGAG others(5): Show |
T | 3 | a0001c0001t0002 a0001c0002t0002 a0002c0003t0002 |
11 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*126_*137delGCTCGC others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 126 | chr14 | 92704181 | ||||||
chr14:92704284 | GCTCACA | G | 3 | a0001c0001t0004 a0002c0003t0004 a0002c0003t0006 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29_*34delTGTGAG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 29 | chr14 | 92704284 | ||||||
chr14:92704316 | T | A | 2 | a0002c0015t0003 a0005c0010t0003 |
3 | HG02258.hp2 HG02615.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 14/14 | 3 | chr14 | 92704316 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:92704373 | A | G | 1 | a0001c0001t0001g0349 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1260-12T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704373 | |||||||
chr14:92704396 | T | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1260-35A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704396 | |||||||
chr14:92704463 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1260-102G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704463 | |||||||
chr14:92704464 | G | C | 1 | a0002c0003t0001g0073 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1260-103C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704464 | |||||||
chr14:92704521 | A | G | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1259+119T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704521 | |||||||
chr14:92704556 | A | C | 294 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(291): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1259+84T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704556 | |||||||
chr14:92704621 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1259+19A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704621 | |||||||
chr14:92704631 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0038 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259+9T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 13/13 | chr14 | 92704631 | |||||||
chr14:92704927 | C | T | 1 | a0002c0003t0001g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1192-220G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92704927 | |||||||
chr14:92704978 | C | T | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1192-271G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92704978 | |||||||
chr14:92705001 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1192-294C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705001 | |||||||
chr14:92705016 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1192-309C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705016 | |||||||
chr14:92705048 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1192-341G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705048 | |||||||
chr14:92705054 | C | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1192-347G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705054 | |||||||
chr14:92705067 | C | T | 3 | a0001c0001t0004g0031 a0002c0003t0004g0146 a0002c0003t0006g0185 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1192-360G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705067 | |||||||
chr14:92705114 | C | T | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1192-407G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705114 | |||||||
chr14:92705175 | A | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0096 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1192-468T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705175 | |||||||
chr14:92705208 | A | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(186): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1192-501T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705208 | |||||||
chr14:92705305 | C | T | 1 | a0001c0002t0001g0282 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1192-598G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705305 | |||||||
chr14:92705388 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1192-681C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705388 | |||||||
chr14:92705502 | A | AAAAC | 92 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0002t0001g0010 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1192-799_1192-796d others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705502 | |||||||
chr14:92705518 | C | A | 3 | a0001c0014t0001g0033 a0001c0014t0001g0047 a0002c0015t0003g0041 |
3 | HG02615.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1192-811G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705518 | |||||||
chr14:92705518 | C | CAAAA | 8 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192-815_1192-812d others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705518 | |||||||
chr14:92705699 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG02080.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1191+784G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705699 | |||||||
chr14:92705703 | T | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0235 |
2 | HG02080.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1191+780A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705703 | |||||||
chr14:92705773 | G | A | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1191+710C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92705773 | |||||||
chr14:92706082 | A | G | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1191+401T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706082 | |||||||
chr14:92706165 | G | A | 2 | a0002c0005t0001g0122 a0002c0005t0001g0189 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1191+318C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706165 | |||||||
chr14:92706182 | G | A | 2 | a0001c0002t0001g0091 a0002c0005t0001g0184 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1191+301C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706182 | |||||||
chr14:92706186 | G | T | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1191+297C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706186 | |||||||
chr14:92706226 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1191+257T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706226 | |||||||
chr14:92706281 | T | C | 3 | a0001c0001t0004g0031 a0002c0003t0004g0146 a0002c0003t0006g0185 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1191+202A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706281 | |||||||
chr14:92706370 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1191+113C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706370 | |||||||
chr14:92706390 | C | A | 31 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(28): Show |
31 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.1191+93G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 12/13 | chr14 | 92706390 | |||||||
chr14:92706665 | C | T | 34 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0169 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1021-12G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706665 | |||||||
chr14:92706668 | G | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0303 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1021-15C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706668 | |||||||
chr14:92706698 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1021-45C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706698 | |||||||
chr14:92706721 | T | A | 3 | a0001c0001t0004g0031 a0002c0003t0004g0146 a0002c0003t0006g0185 |
3 | HG02809.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1021-68A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706721 | |||||||
chr14:92706787 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1021-134T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706787 | |||||||
chr14:92706910 | G | A | 2 | a0001c0002t0001g0223 a0001c0002t0001g0401 |
2 | HG02257.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1021-257C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706910 | |||||||
chr14:92706936 | T | A | 1 | a0001c0002t0002g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1021-283A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706936 | |||||||
chr14:92706959 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0301 a0001c0001t0001g0303 |
3 | HG02895.hp2 HG02897.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1021-306G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706959 | |||||||
chr14:92706993 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1021-340T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92706993 | |||||||
chr14:92707128 | G | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021-475C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707128 | |||||||
chr14:92707143 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(285): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1021-490A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707143 | |||||||
chr14:92707179 | G | C | 1 | a0001c0001t0001g0318 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1021-526C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707179 | |||||||
chr14:92707180 | C | G | 1 | a0001c0001t0001g0318 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1021-527G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707180 | |||||||
chr14:92707249 | T | TA | 268 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1021-597dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707249 | |||||||
chr14:92707249 | T | TAA | 6 | a0001c0001t0001g0060 a0001c0001t0001g0206 a0001c0001t0001g0211 others(3): Show |
6 | HG04199.hp1 NA18953.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.1021-598_1021-597d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707249 | |||||||
chr14:92707255 | A | G | 3 | a0001c0001t0001g0183 a0002c0003t0001g0307 a0002c0003t0001g0308 |
3 | HG03486.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1021-602T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707255 | |||||||
chr14:92707296 | G | A | 42 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(39): Show |
43 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1021-643C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707296 | |||||||
chr14:92707450 | T | C | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1021-797A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707450 | |||||||
chr14:92707507 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1021-854C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707507 | |||||||
chr14:92707515 | C | G | 285 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0023 others(282): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1021-862G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707515 | |||||||
chr14:92707556 | G | A | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1021-903C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707556 | |||||||
chr14:92707637 | C | A | 8 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0001c0017t0001g0095 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-984G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707637 | |||||||
chr14:92707699 | TTAAA | T | 8 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0187 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021-1050_1021-104 others(8): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707699 | |||||||
chr14:92707879 | C | A | 1 | a0002c0005t0001g0348 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1021-1226G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707879 | |||||||
chr14:92707906 | C | T | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1021-1253G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707906 | |||||||
chr14:92707934 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1021-1281A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707934 | |||||||
chr14:92707967 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1021-1314G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707967 | |||||||
chr14:92707988 | C | T | 76 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(73): Show |
76 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1021-1335G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707988 | |||||||
chr14:92707990 | A | T | 1 | a0001c0001t0001g0318 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1021-1337T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92707990 | |||||||
chr14:92708075 | C | T | 1 | a0002c0003t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1021-1422G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708075 | |||||||
chr14:92708105 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1021-1452G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708105 | |||||||
chr14:92708106 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(283): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1021-1453T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708106 | |||||||
chr14:92708151 | C | CA | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0038 others(13): Show |
16 | HG00741.hp1 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1021-1499dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708151 | |||||||
chr14:92708151 | CA | C | 276 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(273): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1021-1499delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708151 | |||||||
chr14:92708248 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1020+1424A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708248 | |||||||
chr14:92708358 | A | C | 187 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1020+1314T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708358 | |||||||
chr14:92708627 | G | A | 92 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(89): Show |
92 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1020+1045C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708627 | |||||||
chr14:92708675 | G | C | 80 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(77): Show |
80 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1020+997C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708675 | |||||||
chr14:92708715 | G | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0344 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1020+957C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708715 | |||||||
chr14:92708856 | C | CA | 22 | a0001c0001t0001g0050 a0001c0001t0001g0107 a0001c0001t0001g0111 others(19): Show |
22 | HG00423.hp2 HG00621.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1020+815dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAA | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0001t0002g0187 others(3): Show |
6 | HG02486.hp2 HG02818.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.1020+810_1020+815d others(8): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA | 31 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0056 others(28): Show |
31 | HG00597.hp2 HG02055.hp2 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.1020+809_1020+815d others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0072 a0001c0001t0001g0128 a0001c0001t0001g0138 others(11): Show |
14 | HG02027.hp1 HG02135.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1020+808_1020+815d others(10): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(2): Show |
24 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0206 others(21): Show |
24 | HG00621.hp1 HG00738.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1020+807_1020+815d others(11): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(3): Show |
28 | a0001c0001t0001g0169 a0001c0001t0001g0235 a0001c0001t0001g0256 others(25): Show |
28 | HG01256.hp1 HG01258.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.1020+806_1020+815d others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(4): Show |
30 | a0001c0001t0001g0232 a0001c0001t0001g0255 a0001c0001t0001g0338 others(27): Show |
30 | HG00099.hp2 HG00639.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1020+805_1020+815d others(13): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(5): Show |
17 | a0001c0002t0001g0051 a0001c0002t0001g0076 a0001c0002t0001g0196 others(14): Show |
17 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.1020+804_1020+815d others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(6): Show |
4 | a0001c0002t0001g0227 a0001c0002t0001g0277 a0001c0002t0001g0406 others(1): Show |
4 | HG01928.hp1 HG01928.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1020+803_1020+815d others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(8): Show |
1 | a0002c0005t0001g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1020+801_1020+815d others(17): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(9): Show |
1 | a0002c0005t0001g0036 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1020+800_1020+815d others(18): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0002g0367 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1020+799_1020+815d others(19): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(11): Show |
1 | a0001c0002t0002g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1020+798_1020+815d others(20): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0369 a0001c0002t0002g0368 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1020+797_1020+815d others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | C | CAGAAAAA others(4): Show |
1 | a0001c0001t0001g0288 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1020+815_1020+816i others(13): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | CA | C | 16 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0208 others(13): Show |
16 | HG00438.hp1 HG00438.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1020+815delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | CAA | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(24): Show |
29 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1020+814_1020+815d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | CAAAA | C | 11 | a0001c0001t0001g0273 a0001c0001t0001g0306 a0001c0002t0001g0091 others(8): Show |
11 | HG00558.hp1 HG02083.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1020+812_1020+815d others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92708856 | CAAAAA | C | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0045 others(61): Show |
66 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1020+811_1020+815d others(7): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92708856 | |||||||
chr14:92709284 | C | G | 8 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0001c0017t0001g0095 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1020+388G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709284 | |||||||
chr14:92709407 | A | G | 1 | a0001c0002t0001g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1020+265T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709407 | |||||||
chr14:92709421 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1020+251G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709421 | |||||||
chr14:92709435 | T | C | 282 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1020+237A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709435 | |||||||
chr14:92709534 | C | T | 8 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0001c0017t0001g0095 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1020+138G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709534 | |||||||
chr14:92709565 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1020+107G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709565 | |||||||
chr14:92709591 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1020+81C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709591 | |||||||
chr14:92709628 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0001g0230 a0001c0001t0001g0313 others(5): Show |
9 | NA18950.hp2 NA18960.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.1020+44C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 11/13 | chr14 | 92709628 | |||||||
chr14:92709899 | C | T | 1 | a0002c0005t0008g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.820-27G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92709899 | |||||||
chr14:92709904 | G | A | 1 | a0002c0005t0001g0036 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.820-32C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92709904 | |||||||
chr14:92709945 | A | C | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.820-73T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92709945 | |||||||
chr14:92709945 | A | G | 6 | a0001c0001t0001g0264 a0001c0014t0001g0033 a0001c0014t0001g0047 others(3): Show |
6 | HG01255.hp2 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-73T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92709945 | |||||||
chr14:92710014 | G | A | 1 | a0001c0001t0001g0404 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.820-142C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710014 | |||||||
chr14:92710046 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.820-174G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710046 | |||||||
chr14:92710346 | G | C | 1 | a0002c0003t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-474C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710346 | |||||||
chr14:92710362 | C | T | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.820-490G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710362 | |||||||
chr14:92710369 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.820-497C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710369 | |||||||
chr14:92710414 | C | G | 1 | a0001c0001t0001g0346 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.820-542G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710414 | |||||||
chr14:92710585 | A | G | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.820-713T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710585 | |||||||
chr14:92710618 | C | A | 2 | a0001c0002t0001g0094 a0001c0002t0001g0096 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.820-746G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710618 | |||||||
chr14:92710619 | C | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0096 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.820-747G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710619 | |||||||
chr14:92710635 | T | C | 7 | a0001c0002t0001g0202 a0001c0002t0001g0214 a0001c0002t0001g0222 others(4): Show |
7 | HG01433.hp1 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-763A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710635 | |||||||
chr14:92710737 | G | A | 2 | a0002c0003t0001g0092 a0002c0003t0001g0121 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.820-865C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710737 | |||||||
chr14:92710743 | C | T | 2 | a0001c0012t0001g0160 a0001c0012t0001g0163 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.820-871G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710743 | |||||||
chr14:92710810 | T | C | 2 | a0002c0005t0001g0122 a0002c0005t0001g0189 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.819+849A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710810 | |||||||
chr14:92710880 | T | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+779A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710880 | |||||||
chr14:92710956 | C | T | 280 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(277): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.819+703G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92710956 | |||||||
chr14:92711055 | C | T | 140 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(137): Show |
141 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.819+604G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711055 | |||||||
chr14:92711078 | T | TAGCCCCA others(3): Show |
1 | a0001c0002t0001g0241 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.819+571_819+580dup others(10): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711078 | |||||||
chr14:92711259 | T | G | 79 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0230 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.819+400A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711259 | |||||||
chr14:92711306 | T | C | 329 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(326): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.819+353A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711306 | |||||||
chr14:92711365 | C | T | 17 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(14): Show |
17 | HG02027.hp1 NA18939.hp1 NA18953.hp1 others(14): Show |
intron_variant | MODIFIER | c.819+294G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711365 | |||||||
chr14:92711386 | CTTGTACG others(7): Show |
C | 1 | a0001c0001t0001g0318 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.819+259_819+272del others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711386 | |||||||
chr14:92711418 | C | T | 3 | a0001c0004t0001g0021 a0001c0004t0001g0084 a0001c0004t0001g0339 |
3 | NA18947.hp2 NA18971.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.819+241G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711418 | |||||||
chr14:92711475 | C | G | 1 | a0002c0003t0001g0087 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.819+184G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711475 | |||||||
chr14:92711475 | C | T | 1 | a0001c0004t0001g0295 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.819+184G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711475 | |||||||
chr14:92711638 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.819+21G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711638 | |||||||
chr14:92711640 | C | A | 2 | a0001c0001t0004g0031 a0002c0003t0006g0185 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.819+19G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 10/13 | chr14 | 92711640 | |||||||
chr14:92711777 | T | C | 1 | a0002c0003t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.730-29A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 9/13 | chr14 | 92711777 | |||||||
chr14:92711796 | G | A | 5 | a0001c0004t0001g0252 a0001c0004t0001g0381 a0001c0008t0001g0034 others(2): Show |
5 | HG00438.hp2 HG01081.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+41C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 9/13 | chr14 | 92711796 | |||||||
chr14:92711959 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.611-4G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92711959 | |||||||
chr14:92711976 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.611-21A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92711976 | |||||||
chr14:92712065 | T | C | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.611-110A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712065 | |||||||
chr14:92712086 | G | A | 2 | a0004c0013t0001g0162 a0004c0013t0001g0384 |
2 | HG01099.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.611-131C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712086 | |||||||
chr14:92712122 | C | T | 80 | a0001c0001t0001g0038 a0001c0001t0001g0230 a0001c0001t0001g0271 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.611-167G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712122 | |||||||
chr14:92712187 | A | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.611-232T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712187 | |||||||
chr14:92712353 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.611-398T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712353 | |||||||
chr14:92712435 | T | C | 82 | a0001c0001t0001g0038 a0001c0001t0001g0088 a0001c0001t0001g0230 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.610+370A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712435 | |||||||
chr14:92712637 | G | A | 1 | a0002c0003t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.610+168C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712637 | |||||||
chr14:92712748 | G | A | 1 | a0001c0001t0001g0383 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.610+57C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712748 | |||||||
chr14:92712780 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.610+25G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 8/13 | chr14 | 92712780 | |||||||
chr14:92712915 | G | A | 1 | a0001c0002t0001g0393 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.544-44C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92712915 | |||||||
chr14:92713077 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0303 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.544-206G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713077 | |||||||
chr14:92713133 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.544-262C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713133 | |||||||
chr14:92713197 | C | T | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | NA18942.hp1 NA18986.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-326G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713197 | |||||||
chr14:92713234 | T | G | 1 | a0001c0002t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-363A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713234 | |||||||
chr14:92713337 | C | T | 1 | a0001c0001t0001g0402 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.544-466G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713337 | |||||||
chr14:92713583 | G | A | 11 | a0001c0001t0001g0301 a0001c0001t0001g0303 a0001c0001t0001g0369 others(8): Show |
11 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+240C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713583 | |||||||
chr14:92713612 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.543+211C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713612 | |||||||
chr14:92713727 | C | T | 1 | a0001c0001t0001g0377 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.543+96G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713727 | |||||||
chr14:92713807 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.543+16G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 7/13 | chr14 | 92713807 | |||||||
chr14:92713945 | C | T | 8 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0001c0017t0001g0095 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-60G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/13 | chr14 | 92713945 | |||||||
chr14:92713962 | T | C | 1 | a0001c0002t0001g0391 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.481-77A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/13 | chr14 | 92713962 | |||||||
chr14:92713984 | T | C | 1 | a0001c0001t0001g0383 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.481-99A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/13 | chr14 | 92713984 | |||||||
chr14:92714238 | G | A | 1 | a0001c0004t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.480+138C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/13 | chr14 | 92714238 | |||||||
chr14:92714332 | T | C | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.480+44A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 6/13 | chr14 | 92714332 | |||||||
chr14:92714468 | G | A | 1 | a0001c0001t0001g0402 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.405-17C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714468 | |||||||
chr14:92714472 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.405-21C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714472 | |||||||
chr14:92714584 | C | A | 1 | a0002c0003t0004g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.405-133G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714584 | |||||||
chr14:92714590 | C | T | 1 | a0001c0004t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.405-139G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714590 | |||||||
chr14:92714652 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0145 others(3): Show |
7 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-201A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714652 | |||||||
chr14:92714834 | G | T | 82 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0088 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.405-383C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714834 | |||||||
chr14:92714837 | T | TC | 33 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(30): Show |
33 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.405-387dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714837 | |||||||
chr14:92714842 | C | A | 82 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0088 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.405-391G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714842 | |||||||
chr14:92714842 | C | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(5): Show |
8 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-391G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714842 | |||||||
chr14:92714843 | C | CA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(1): Show |
6 | NA18948.hp1 NA18961.hp1 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-393_405-392ins others(1): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714843 | |||||||
chr14:92714843 | C | G | 5 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0017t0001g0095 others(2): Show |
5 | HG02258.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-392G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714843 | |||||||
chr14:92714863 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
38 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.405-412G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714863 | |||||||
chr14:92714866 | A | AGTCTGGA others(8): Show |
1 | a0001c0001t0001g0398 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.405-430_405-416dup others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714866 | |||||||
chr14:92714883 | A | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(5): Show |
8 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-432T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714883 | |||||||
chr14:92714896 | G | C | 9 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0211 others(6): Show |
9 | NA18939.hp1 NA18953.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-445C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714896 | |||||||
chr14:92714994 | A | AT | 72 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0050 others(69): Show |
74 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.405-544dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714994 | |||||||
chr14:92714994 | AT | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0142 a0001c0001t0001g0144 others(13): Show |
16 | HG00639.hp2 HG01081.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.405-544delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92714994 | |||||||
chr14:92715085 | G | A | 3 | a0001c0002t0001g0227 a0002c0005t0001g0201 a0002c0005t0001g0220 |
3 | HG01496.hp1 HG01928.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.405-634C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715085 | |||||||
chr14:92715111 | G | T | 7 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0002c0005t0001g0099 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-660C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715111 | |||||||
chr14:92715148 | G | A | 5 | a0001c0001t0001g0275 a0002c0003t0001g0001 a0002c0003t0001g0011 others(2): Show |
6 | HG00735.hp1 HG01123.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-697C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715148 | |||||||
chr14:92715210 | G | GGT | 4 | a0001c0001t0001g0369 a0001c0002t0002g0098 a0001c0002t0002g0367 others(1): Show |
4 | HG02572.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-761_405-760dup others(2): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715210 | |||||||
chr14:92715214 | G | GGT | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(52): Show |
57 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(54): Show |
intron_variant | MODIFIER | c.405-765_405-764dup others(2): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | GGTGT | 48 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(45): Show |
50 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.405-767_405-764dup others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | GGTGTGT | 114 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0042 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.405-769_405-764dup others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | GGTGTGTG others(1): Show |
4 | a0001c0001t0001g0287 a0001c0001t0001g0370 a0001c0001t0001g0371 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-771_405-764dup others(8): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | GGTGTGTG others(3): Show |
7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-773_405-764dup others(10): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0005g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.405-775_405-764dup others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715214 | G | T | 6 | a0001c0001t0001g0322 a0001c0001t0001g0369 a0001c0002t0002g0098 others(3): Show |
6 | HG02572.hp1 HG03209.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.405-763C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715214 | |||||||
chr14:92715532 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(5): Show |
8 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+604G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715532 | |||||||
chr14:92715727 | G | A | 7 | a0001c0001t0001g0248 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG02056.hp1 NA18960.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+409C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715727 | |||||||
chr14:92715817 | G | GA | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+318_404+319ins others(1): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715817 | |||||||
chr14:92715818 | C | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(3): Show |
6 | HG01192.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+318G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92715818 | |||||||
chr14:92716121 | G | A | 78 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0229 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(75): Show |
intron_variant | MODIFIER | c.404+15C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 5/13 | chr14 | 92716121 | |||||||
chr14:92716268 | C | G | 1 | a0002c0003t0001g0410 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.319-47G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716268 | |||||||
chr14:92716282 | G | A | 1 | a0001c0008t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.319-61C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716282 | |||||||
chr14:92716298 | C | G | 1 | a0002c0003t0001g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.319-77G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716298 | |||||||
chr14:92716328 | A | G | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.319-107T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716328 | |||||||
chr14:92716383 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.319-162T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716383 | |||||||
chr14:92716399 | G | A | 1 | a0001c0002t0001g0207 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.319-178C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716399 | |||||||
chr14:92716672 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.319-451G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716672 | |||||||
chr14:92716875 | G | C | 2 | a0001c0004t0001g0291 a0001c0004t0001g0376 |
2 | NA19075.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.318+505C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716875 | |||||||
chr14:92716964 | A | G | 1 | a0002c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.318+416T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92716964 | |||||||
chr14:92717141 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.318+239T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92717141 | |||||||
chr14:92717220 | C | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(74): Show |
79 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.318+160G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92717220 | |||||||
chr14:92717373 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
39 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.318+7G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 4/13 | chr14 | 92717373 | |||||||
chr14:92717488 | C | T | 2 | a0001c0001t0004g0031 a0002c0003t0006g0185 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.237-27G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92717488 | |||||||
chr14:92717516 | C | T | 1 | a0002c0003t0001g0075 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.237-55G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92717516 | |||||||
chr14:92717556 | G | A | 1 | a0002c0003t0001g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.237-95C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92717556 | |||||||
chr14:92718109 | G | A | 1 | a0001c0002t0001g0379 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.236+638C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718109 | |||||||
chr14:92718155 | A | G | 2 | a0002c0003t0001g0073 a0002c0003t0001g0077 |
2 | NA19060.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.236+592T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718155 | |||||||
chr14:92718189 | G | A | 41 | a0001c0001t0001g0090 a0001c0001t0001g0142 a0001c0001t0001g0152 others(38): Show |
41 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.236+558C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718189 | |||||||
chr14:92718218 | G | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.236+529C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718218 | |||||||
chr14:92718409 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.236+338T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718409 | |||||||
chr14:92718448 | C | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.236+299G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718448 | |||||||
chr14:92718510 | G | A | 2 | a0002c0003t0001g0008 a0002c0003t0001g0334 |
3 | HG01081.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.236+237C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718510 | |||||||
chr14:92718585 | T | TA | 9 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0001g0307 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.236+161dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718585 | |||||||
chr14:92718588 | A | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0023 others(6): Show |
9 | HG01891.hp2 HG01993.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.236+159T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718588 | |||||||
chr14:92718619 | T | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | NA18977.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.236+128A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 3/13 | chr14 | 92718619 | |||||||
chr14:92718938 | A | C | 2 | a0002c0003t0001g0008 a0002c0003t0001g0334 |
3 | HG01081.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.139-94T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92718938 | |||||||
chr14:92718952 | C | CCT | 98 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(95): Show |
100 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.139-109_139-108ins others(2): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92718952 | |||||||
chr14:92718991 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-147G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92718991 | |||||||
chr14:92719076 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
39 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.139-232G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719076 | |||||||
chr14:92719108 | A | G | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-264T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719108 | |||||||
chr14:92719127 | A | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG02683.hp1 HG03654.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-283T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719127 | |||||||
chr14:92719129 | C | T | 4 | a0001c0001t0001g0127 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG02683.hp1 HG03654.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-285G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719129 | |||||||
chr14:92719133 | C | T | 2 | a0002c0003t0001g0307 a0002c0003t0001g0308 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.139-289G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719133 | |||||||
chr14:92719134 | G | A | 4 | a0001c0001t0001g0127 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG02683.hp1 HG03654.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-290C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719134 | |||||||
chr14:92719140 | GCCACCAC others(17): Show |
G | 41 | a0001c0001t0001g0090 a0001c0001t0001g0142 a0001c0001t0001g0152 others(38): Show |
41 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.139-320_139-297del others(24): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719140 | |||||||
chr14:92719152 | G | A | 3 | a0002c0003t0001g0333 a0005c0010t0003g0027 a0005c0010t0003g0093 |
3 | HG02258.hp2 HG02523.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-308C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719152 | |||||||
chr14:92719155 | ACTG | A | 5 | a0001c0001t0004g0031 a0002c0003t0001g0307 a0002c0003t0001g0308 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-314_139-312del others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719155 | |||||||
chr14:92719157 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(112): Show |
119 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.139-313A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719157 | |||||||
chr14:92719158 | G | A | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-314C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719158 | |||||||
chr14:92719158 | G | GCCA | 115 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
119 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.139-317_139-315dup others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719158 | |||||||
chr14:92719158 | GCCACCAC others(2): Show |
G | 70 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(67): Show |
71 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.139-323_139-315del others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719158 | |||||||
chr14:92719159 | CCACCACC others(221): Show |
C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-543_139-316del | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719159 | |||||||
chr14:92719161 | A | G | 5 | a0001c0001t0004g0031 a0002c0003t0001g0307 a0002c0003t0001g0308 others(2): Show |
5 | HG02809.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-317T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719161 | |||||||
chr14:92719162 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-318G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719162 | |||||||
chr14:92719164 | A | G | 6 | a0001c0001t0001g0180 a0001c0001t0001g0212 a0001c0001t0001g0396 others(3): Show |
6 | HG02040.hp2 HG02486.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-320T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719164 | |||||||
chr14:92719176 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-332T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719176 | |||||||
chr14:92719180 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-336G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719180 | |||||||
chr14:92719183 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-339A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719183 | |||||||
chr14:92719183 | TCACCACC others(29): Show |
T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-375_139-340del others(36): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719183 | |||||||
chr14:92719188 | A | G | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.139-344T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719188 | |||||||
chr14:92719201 | A | C | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-357T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719201 | |||||||
chr14:92719201 | A | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-357T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719201 | |||||||
chr14:92719206 | A | G | 48 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(45): Show |
50 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.139-362T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719206 | |||||||
chr14:92719207 | C | A | 9 | a0001c0001t0001g0369 a0001c0001t0004g0031 a0001c0002t0002g0098 others(6): Show |
9 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-363G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719207 | |||||||
chr14:92719209 | A | ACCGCCAC others(5): Show |
5 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(2): Show |
5 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-366_139-365ins others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719209 | |||||||
chr14:92719209 | A | G | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.139-365T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719209 | |||||||
chr14:92719211 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.139-367G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719211 | |||||||
chr14:92719219 | ACACCACC others(23): Show |
A | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-405_139-376del others(30): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719219 | |||||||
chr14:92719224 | A | ACCACCG | 6 | a0001c0004t0001g0022 a0001c0004t0001g0295 a0001c0004t0001g0319 others(3): Show |
6 | HG00609.hp2 HG01978.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-386_139-381dup others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719224 | |||||||
chr14:92719224 | A | G | 3 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0017t0001g0095 |
3 | HG02486.hp1 HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-380T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719224 | |||||||
chr14:92719227 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-383T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719227 | |||||||
chr14:92719230 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-386C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719230 | |||||||
chr14:92719230 | GCCACCGC others(2): Show |
G | 9 | a0001c0001t0001g0275 a0001c0001t0004g0031 a0002c0003t0001g0001 others(6): Show |
10 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.139-395_139-387del others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719230 | |||||||
chr14:92719230 | GCCACCGC others(17): Show |
G | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.139-410_139-387del others(24): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719230 | |||||||
chr14:92719236 | G | A | 2 | a0001c0001t0001g0244 a0002c0003t0001g0110 |
2 | HG00280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.139-392C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719236 | |||||||
chr14:92719236 | GCCA | G | 67 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(64): Show |
68 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.139-395_139-393del others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719236 | |||||||
chr14:92719236 | GCCACCAC others(8): Show |
G | 3 | a0001c0001t0001g0296 a0001c0001t0001g0397 a0001c0002t0001g0265 |
3 | NA18955.hp1 NA18977.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.139-407_139-393del others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719236 | |||||||
chr14:92719236 | GCCACCAC others(11): Show |
G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
71 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.139-410_139-393del others(18): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719236 | |||||||
chr14:92719237 | C | A | 2 | a0001c0001t0001g0244 a0002c0003t0001g0110 |
2 | HG00280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.139-393G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719237 | |||||||
chr14:92719239 | ACCACCGC others(14): Show |
A | 1 | a0001c0001t0001g0388 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.139-416_139-396del others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719239 | ACCACCGC others(23): Show |
A | 2 | a0001c0001t0001g0111 a0004c0013t0001g0162 |
2 | HG03239.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.139-425_139-396del others(30): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719239 | ACCACCGC others(26): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.139-428_139-396del others(33): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719239 | ACCACCGC others(38): Show |
A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0264 a0002c0003t0001g0029 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-440_139-396del others(45): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719239 | ACCACCGC others(41): Show |
A | 1 | a0001c0014t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.139-443_139-396del others(48): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719239 | ACCACCGC others(53): Show |
A | 1 | a0002c0005t0001g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.139-455_139-396del others(60): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719239 | |||||||
chr14:92719242 | A | G | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(142): Show |
147 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.139-398T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719242 | |||||||
chr14:92719245 | G | A | 79 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(76): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.139-401C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719245 | |||||||
chr14:92719248 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0002c0003t0001g0110 |
3 | HG00280.hp2 HG03453.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.139-404T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719248 | |||||||
chr14:92719248 | ACCACCAC others(5): Show |
A | 5 | a0001c0001t0001g0298 a0001c0001t0001g0310 a0001c0001t0001g0343 others(2): Show |
5 | HG00323.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-416_139-405del others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719248 | |||||||
chr14:92719248 | ACCACCAC others(11): Show |
A | 1 | a0001c0001t0001g0289 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.139-422_139-405del others(18): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719248 | |||||||
chr14:92719248 | ACCACCAC others(14): Show |
A | 34 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0142 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG01358.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-425_139-405del others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719248 | |||||||
chr14:92719248 | ACCACCAC others(32): Show |
A | 1 | a0001c0001t0001g0390 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.139-443_139-405del others(39): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719248 | |||||||
chr14:92719249 | CCACCACC others(19): Show |
C | 1 | a0004c0013t0001g0384 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.139-431_139-406del others(26): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719249 | |||||||
chr14:92719251 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(129): Show |
135 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.139-407T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719251 | |||||||
chr14:92719251 | ACCACCAC others(10): Show |
A | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.139-424_139-408del others(17): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719251 | |||||||
chr14:92719251 | ACCACCAC others(14): Show |
A | 4 | a0001c0001t0001g0058 a0001c0001t0001g0336 a0002c0003t0001g0083 others(1): Show |
4 | HG02074.hp2 HG02145.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-428_139-408del others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719251 | |||||||
chr14:92719254 | A | G | 64 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0038 others(61): Show |
66 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.139-410T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719254 | |||||||
chr14:92719257 | A | ACCACCGC others(20): Show |
1 | a0001c0001t0002g0187 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.139-414_139-413ins others(27): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719257 | |||||||
chr14:92719257 | A | G | 80 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(77): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.139-413T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719257 | |||||||
chr14:92719257 | ACCGCCAC others(8): Show |
A | 1 | a0001c0002t0001g0282 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.139-428_139-414del others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719257 | |||||||
chr14:92719257 | ACCGCCAC others(20): Show |
A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(4): Show |
9 | NA18942.hp1 NA18948.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-440_139-414del others(27): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719257 | |||||||
chr14:92719260 | G | A | 75 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.139-416C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719260 | |||||||
chr14:92719260 | G | C | 1 | a0003c0007t0001g0177 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.139-416C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719260 | |||||||
chr14:92719260 | GCCA | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0205 a0001c0001t0001g0231 |
3 | HG00673.hp2 NA18993.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.139-419_139-417del others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719260 | |||||||
chr14:92719261 | CCACCGCC others(7): Show |
C | 1 | a0002c0003t0001g0078 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.139-431_139-418del others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719261 | |||||||
chr14:92719263 | A | G | 36 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(33): Show |
36 | HG00597.hp2 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.139-419T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719263 | |||||||
chr14:92719263 | ACCGCCG | A | 65 | a0001c0001t0001g0038 a0001c0001t0001g0229 a0001c0001t0001g0230 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.139-425_139-420del others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719263 | |||||||
chr14:92719263 | ACCGCCGC others(5): Show |
A | 10 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 others(7): Show |
10 | HG02055.hp2 HG02109.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-431_139-420del others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719263 | |||||||
chr14:92719263 | ACCGCCGC others(11): Show |
A | 5 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0002c0005t0001g0099 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-437_139-420del others(18): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719263 | |||||||
chr14:92719263 | ACCGCCGC others(29): Show |
A | 1 | a0002c0005t0001g0122 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139-455_139-420del others(36): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719263 | |||||||
chr14:92719264 | CCGCCGCC others(13): Show |
C | 1 | a0001c0001t0001g0358 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.139-440_139-421del others(20): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719264 | |||||||
chr14:92719266 | G | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
79 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.139-422C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719266 | |||||||
chr14:92719269 | G | A | 5 | a0001c0001t0001g0275 a0001c0001t0002g0188 a0002c0003t0001g0001 others(2): Show |
6 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-425C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719269 | |||||||
chr14:92719269 | G | GCCA | 7 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0004t0001g0237 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-426_139-425ins others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719269 | |||||||
chr14:92719269 | G | GCCAC | 3 | a0001c0004t0001g0022 a0001c0004t0001g0319 a0002c0006t0001g0089 |
3 | HG00609.hp2 HG01978.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.139-426_139-425ins others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719269 | |||||||
chr14:92719271 | C | CACT | 24 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0072 others(21): Show |
24 | HG00597.hp2 HG02027.hp1 HG02135.hp1 others(21): Show |
intron_variant | MODIFIER | c.139-428_139-427ins others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719271 | |||||||
chr14:92719272 | G | A | 16 | a0001c0001t0001g0143 a0001c0001t0001g0273 a0001c0001t0001g0275 others(13): Show |
17 | HG00735.hp1 HG00741.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-428C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719272 | |||||||
chr14:92719272 | GCCGCCA | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0369 a0001c0002t0002g0098 others(2): Show |
5 | HG02572.hp1 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-434_139-429del others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719272 | |||||||
chr14:92719272 | GCCGCCAC others(23): Show |
G | 27 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0054 others(24): Show |
28 | HG00280.hp1 HG00423.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.139-458_139-429del others(30): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719272 | |||||||
chr14:92719273 | CCGCCA | C | 3 | a0001c0002t0001g0326 a0002c0005t0001g0036 a0002c0005t0001g0037 |
3 | HG00741.hp2 HG01099.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.139-434_139-430del others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719273 | |||||||
chr14:92719275 | G | A | 6 | a0001c0001t0001g0111 a0001c0001t0001g0205 a0001c0001t0001g0298 others(3): Show |
6 | HG00323.hp1 HG00673.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-431C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719275 | |||||||
chr14:92719275 | GCCA | G | 5 | a0001c0001t0001g0273 a0001c0002t0001g0094 a0001c0002t0001g0096 others(2): Show |
5 | HG02083.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-434_139-432del others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719275 | |||||||
chr14:92719275 | GCCACCGC others(20): Show |
G | 3 | a0001c0001t0001g0321 a0001c0001t0001g0346 a0001c0017t0001g0095 |
3 | HG00597.hp1 HG02486.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.139-458_139-432del others(27): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719275 | |||||||
chr14:92719277 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.139-433G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719277 | |||||||
chr14:92719278 | A | G | 78 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0060 others(75): Show |
79 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.139-434T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719278 | |||||||
chr14:92719278 | ACCGCCG | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
70 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.139-440_139-435del others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719278 | |||||||
chr14:92719279 | CCGCCGCC others(16): Show |
C | 1 | a0001c0001t0001g0231 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.139-458_139-436del others(23): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719279 | |||||||
chr14:92719281 | G | A | 6 | a0001c0001t0001g0107 a0002c0003t0001g0011 a0002c0003t0001g0101 others(3): Show |
6 | HG00735.hp1 HG02735.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-437C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719281 | |||||||
chr14:92719281 | GCCGCCGC others(14): Show |
G | 1 | a0001c0001t0001g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.139-458_139-438del others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719281 | |||||||
chr14:92719284 | G | A | 16 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0275 others(13): Show |
17 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.139-440C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719284 | |||||||
chr14:92719284 | G | T | 1 | a0002c0003t0001g0011 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.139-440C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719284 | |||||||
chr14:92719287 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
188 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.139-443C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719287 | |||||||
chr14:92719290 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-446C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719290 | |||||||
chr14:92719290 | G | T | 4 | a0001c0001t0001g0275 a0002c0003t0001g0001 a0002c0003t0001g0086 others(1): Show |
5 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.139-446C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719290 | |||||||
chr14:92719293 | G | A | 34 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0090 others(31): Show |
34 | HG00323.hp1 HG00609.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.139-449C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719293 | |||||||
chr14:92719293 | G | GCCACCCG others(3): Show |
1 | a0001c0004t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.139-450_139-449ins others(10): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719293 | |||||||
chr14:92719296 | G | A | 76 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(73): Show |
76 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.139-452C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719296 | |||||||
chr14:92719296 | GCCGCCAC others(23): Show |
G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0313 a0001c0001t0001g0314 others(4): Show |
8 | NA18950.hp2 NA18960.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.139-482_139-453del others(30): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719296 | |||||||
chr14:92719297 | CCGCCA | C | 4 | a0002c0003t0001g0011 a0002c0005t0001g0030 a0002c0005t0001g0112 others(1): Show |
4 | HG00735.hp1 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-458_139-454del others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719297 | |||||||
chr14:92719299 | G | A | 32 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0169 others(29): Show |
32 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.139-455C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719299 | |||||||
chr14:92719302 | A | AC | 3 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0002c0006t0001g0150 |
3 | HG02055.hp2 NA19000.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.139-459dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719302 | |||||||
chr14:92719302 | A | G | 48 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0111 others(45): Show |
48 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.139-458T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719302 | |||||||
chr14:92719302 | ACCGCCGC others(8): Show |
A | 3 | a0001c0001t0001g0310 a0001c0001t0001g0344 a0002c0003t0001g0123 |
3 | HG01516.hp1 HG01517.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.139-473_139-459del others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719302 | |||||||
chr14:92719308 | G | A | 22 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0140 others(19): Show |
22 | HG00408.hp1 HG00423.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.139-464C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719308 | |||||||
chr14:92719309 | C | T | 1 | a0002c0003t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.139-465G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719309 | |||||||
chr14:92719309 | CCACCGCC others(23): Show |
C | 50 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(47): Show |
50 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-495_139-466del others(30): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719309 | |||||||
chr14:92719311 | A | AC | 3 | a0001c0001t0001g0072 a0001c0002t0001g0010 a0001c0004t0001g0124 |
3 | HG01175.hp1 NA18985.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.139-468dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719311 | |||||||
chr14:92719311 | A | G | 53 | a0001c0001t0001g0042 a0001c0001t0001g0090 a0001c0001t0001g0135 others(50): Show |
53 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.139-467T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719311 | |||||||
chr14:92719311 | ACCGCCG | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(67): Show |
75 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.139-473_139-468del others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719311 | |||||||
chr14:92719312 | CCGCCG | C | 3 | a0001c0001t0001g0336 a0002c0003t0001g0083 a0002c0003t0001g0410 |
3 | HG02074.hp2 HG02145.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.139-473_139-469del others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719312 | |||||||
chr14:92719312 | CCGCCGCC others(7): Show |
C | 3 | a0001c0001t0001g0343 a0001c0001t0001g0349 a0002c0003t0001g0049 |
3 | HG04228.hp1 NA18961.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.139-482_139-469del others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719312 | |||||||
chr14:92719312 | CCGCCGCC others(22): Show |
C | 1 | a0001c0001t0001g0408 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.139-497_139-469del others(29): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719312 | |||||||
chr14:92719315 | CCGCCGCC others(35): Show |
C | 1 | a0002c0003t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.139-513_139-472del others(42): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719315 | |||||||
chr14:92719317 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(104): Show |
110 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.139-473C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719317 | |||||||
chr14:92719317 | G | GCCACCGC others(3): Show |
1 | a0001c0004t0001g0353 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.139-474_139-473ins others(10): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719317 | |||||||
chr14:92719317 | GCCGCCGC others(8): Show |
G | 1 | a0001c0001t0001g0298 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.139-488_139-474del others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719317 | |||||||
chr14:92719318 | CCGCCGCC others(14): Show |
C | 1 | a0002c0003t0001g0164 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.139-495_139-475del others(21): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719318 | |||||||
chr14:92719320 | G | A | 21 | a0001c0001t0001g0157 a0001c0001t0001g0254 a0001c0001t0007g0215 others(18): Show |
21 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-476C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719320 | |||||||
chr14:92719320 | G | GCCGCCAC others(17): Show |
2 | a0006c0011t0001g0013 a0006c0011t0001g0014 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.139-477_139-476ins others(24): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719320 | |||||||
chr14:92719323 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(71): Show |
76 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.139-479C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719323 | |||||||
chr14:92719323 | G | GCCGCCGC others(12): Show |
1 | a0001c0001t0002g0188 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.139-480_139-479ins others(19): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719323 | |||||||
chr14:92719324 | CCACCGCC others(8): Show |
C | 3 | a0002c0003t0001g0065 a0002c0003t0001g0073 a0002c0003t0001g0074 |
3 | HG02155.hp2 NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.139-495_139-481del others(15): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719324 | |||||||
chr14:92719326 | A | AC | 3 | a0001c0001t0001g0038 a0001c0002t0001g0214 a0001c0002t0001g0278 |
3 | HG01981.hp1 HG03139.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.139-483dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719326 | |||||||
chr14:92719326 | A | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0054 others(28): Show |
32 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.139-482T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719326 | |||||||
chr14:92719327 | CCGCCACC others(7): Show |
C | 1 | a0001c0001t0001g0102 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.139-497_139-484del others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719327 | |||||||
chr14:92719332 | A | ACCACCGC others(2): Show |
17 | a0001c0001t0001g0157 a0001c0004t0001g0021 a0001c0004t0001g0084 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(14): Show |
intron_variant | MODIFIER | c.139-489_139-488ins others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719332 | |||||||
chr14:92719332 | A | ACCACCGC others(4): Show |
1 | a0003c0007t0001g0177 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.139-489_139-488ins others(11): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719332 | |||||||
chr14:92719332 | A | G | 23 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0001c0004t0001g0022 others(20): Show |
23 | HG00609.hp2 HG00735.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.139-488T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719332 | |||||||
chr14:92719332 | ACCGCCAT others(5): Show |
A | 1 | a0002c0003t0001g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.139-500_139-489del others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719332 | |||||||
chr14:92719333 | CCGCCATC others(7): Show |
C | 1 | a0002c0005t0001g0186 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.139-503_139-490del others(14): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719333 | |||||||
chr14:92719335 | G | A | 2 | a0001c0001t0007g0215 a0002c0003t0001g0011 |
2 | HG00735.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.139-491C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719335 | |||||||
chr14:92719338 | A | G | 18 | a0001c0001t0001g0058 a0001c0001t0001g0157 a0001c0001t0001g0275 others(15): Show |
19 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.139-494T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719338 | |||||||
chr14:92719339 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
135 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.139-495A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719339 | |||||||
chr14:92719343 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-499G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719343 | |||||||
chr14:92719347 | A | ACCG | 3 | a0001c0001t0001g0143 a0006c0011t0001g0013 a0006c0011t0001g0014 |
3 | HG03688.hp1 HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.139-504_139-503ins others(3): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719347 | |||||||
chr14:92719348 | C | T | 1 | a0001c0001t0007g0215 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.139-504G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719348 | |||||||
chr14:92719350 | A | G | 6 | a0001c0002t0001g0091 a0001c0002t0001g0204 a0002c0005t0001g0099 others(3): Show |
6 | HG01891.hp1 HG02145.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-506T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719350 | |||||||
chr14:92719351 | C | T | 3 | a0001c0001t0001g0143 a0006c0011t0001g0013 a0006c0011t0001g0014 |
3 | HG03688.hp1 HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.139-507G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719351 | |||||||
chr14:92719353 | A | G | 5 | a0001c0001t0001g0046 a0001c0001t0001g0336 a0001c0001t0001g0382 others(2): Show |
5 | HG00741.hp1 HG02145.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-509T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719353 | |||||||
chr14:92719356 | A | G | 3 | a0001c0001t0001g0143 a0006c0011t0001g0013 a0006c0011t0001g0014 |
3 | HG03688.hp1 HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.139-512T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719356 | |||||||
chr14:92719357 | A | C | 4 | a0001c0001t0001g0143 a0002c0003t0001g0068 a0006c0011t0001g0013 others(1): Show |
4 | HG02135.hp2 HG03688.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-513T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719357 | |||||||
chr14:92719357 | ACACCAC | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-519_139-514del others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719357 | |||||||
chr14:92719368 | A | G | 2 | a0002c0003t0001g0064 a0002c0003t0001g0123 |
2 | HG02165.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.139-524T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719368 | |||||||
chr14:92719368 | ACCACCAA others(5): Show |
A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(30): Show |
35 | HG00597.hp2 HG00673.hp2 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.139-536_139-525del others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719368 | |||||||
chr14:92719369 | C | A | 4 | a0001c0001t0001g0143 a0001c0001t0007g0215 a0006c0011t0001g0013 others(1): Show |
4 | HG03688.hp1 HG03834.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-525G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719369 | |||||||
chr14:92719375 | A | C | 4 | a0001c0001t0001g0143 a0001c0001t0007g0215 a0006c0011t0001g0013 others(1): Show |
4 | HG03688.hp1 HG03834.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-531T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719375 | |||||||
chr14:92719380 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0007g0215 a0006c0011t0001g0013 others(1): Show |
4 | HG03688.hp1 HG03834.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-536C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719380 | |||||||
chr14:92719391 | C | A | 1 | a0002c0005t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.139-547G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719391 | |||||||
chr14:92719399 | A | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-555T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719399 | |||||||
chr14:92719404 | G | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-560C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719404 | |||||||
chr14:92719763 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.139-919A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719763 | |||||||
chr14:92719933 | G | T | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-1089C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92719933 | |||||||
chr14:92720022 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-1178T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720022 | |||||||
chr14:92720061 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.139-1217T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720061 | |||||||
chr14:92720113 | A | G | 3 | a0001c0002t0001g0091 a0002c0005t0001g0184 a0002c0005t0001g0186 |
3 | HG03139.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139-1269T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720113 | |||||||
chr14:92720249 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(75): Show |
80 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.139-1405G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720249 | |||||||
chr14:92720271 | T | G | 3 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0317 |
3 | NA18960.hp1 NA18963.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.139-1427A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720271 | |||||||
chr14:92720273 | G | C | 332 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(329): Show |
341 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(338): Show |
intron_variant | MODIFIER | c.139-1429C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720273 | |||||||
chr14:92720313 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-1469T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720313 | |||||||
chr14:92720410 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.139-1566C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720410 | |||||||
chr14:92720438 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.139-1594G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720438 | |||||||
chr14:92720439 | G | A | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.139-1595C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720439 | |||||||
chr14:92720457 | C | G | 46 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(43): Show |
48 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.139-1613G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720457 | |||||||
chr14:92720572 | T | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(100): Show |
105 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.139-1728A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720572 | |||||||
chr14:92720591 | C | T | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.139-1747G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720591 | |||||||
chr14:92720640 | C | T | 9 | a0001c0001t0001g0369 a0001c0001t0004g0031 a0001c0002t0002g0098 others(6): Show |
9 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-1796G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720640 | |||||||
chr14:92720662 | T | C | 334 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(331): Show |
343 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.139-1818A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720662 | |||||||
chr14:92720665 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0284 a0001c0002t0001g0392 |
3 | HG00642.hp2 HG01192.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.139-1821G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720665 | |||||||
chr14:92720752 | C | CTACAT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
45 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.139-1913_139-1909d others(7): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720752 | |||||||
chr14:92720793 | G | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
83 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.139-1949C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720793 | |||||||
chr14:92720794 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.139-1950G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720794 | |||||||
chr14:92720802 | C | T | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.139-1958G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720802 | |||||||
chr14:92720901 | G | GT | 17 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0001c0002t0001g0091 others(14): Show |
17 | HG00609.hp2 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.139-2058dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92720901 | |||||||
chr14:92721065 | A | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-2221T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721065 | |||||||
chr14:92721093 | T | C | 1 | a0001c0002t0001g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.139-2249A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721093 | |||||||
chr14:92721107 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.139-2263C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721107 | |||||||
chr14:92721133 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-2289G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721133 | |||||||
chr14:92721137 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.139-2293G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721137 | |||||||
chr14:92721182 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.139-2338C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721182 | |||||||
chr14:92721298 | T | C | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-2454A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721298 | |||||||
chr14:92721443 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
143 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.139-2599G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721443 | |||||||
chr14:92721481 | A | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-2637T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721481 | |||||||
chr14:92721564 | T | C | 1 | a0001c0002t0001g0379 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.139-2720A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721564 | |||||||
chr14:92721739 | C | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.139-2895G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721739 | |||||||
chr14:92721756 | A | T | 1 | a0002c0005t0001g0387 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.139-2912T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721756 | |||||||
chr14:92721769 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.139-2925T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721769 | |||||||
chr14:92721880 | C | A | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-3036G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721880 | |||||||
chr14:92721910 | G | A | 3 | a0002c0003t0001g0307 a0002c0003t0001g0308 a0002c0003t0004g0146 |
3 | HG03486.hp1 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.139-3066C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721910 | |||||||
chr14:92721923 | A | G | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-3079T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92721923 | |||||||
chr14:92722174 | A | ATTT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-3333_139-3331d others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722174 | |||||||
chr14:92722262 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-3418A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722262 | |||||||
chr14:92722509 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0151 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.139-3665C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722509 | |||||||
chr14:92722531 | CCGAGATT others(11): Show |
C | 51 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0090 others(48): Show |
52 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.139-3705_139-3688d others(20): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722531 | |||||||
chr14:92722541 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-3697T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722541 | |||||||
chr14:92722562 | C | T | 4 | a0001c0001t0001g0104 a0001c0001t0001g0108 a0001c0001t0001g0386 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-3718G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722562 | |||||||
chr14:92722773 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.139-3929A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722773 | |||||||
chr14:92722852 | C | T | 1 | a0001c0017t0001g0095 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.139-4008G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722852 | |||||||
chr14:92722858 | T | C | 4 | a0001c0001t0001g0369 a0001c0002t0002g0098 a0001c0002t0002g0367 others(1): Show |
4 | HG02572.hp1 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-4014A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722858 | |||||||
chr14:92722910 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0183 others(6): Show |
9 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.139-4066G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722910 | |||||||
chr14:92722911 | G | A | 3 | a0001c0008t0001g0034 a0001c0008t0001g0043 a0001c0008t0001g0044 |
3 | HG02451.hp2 HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.139-4067C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722911 | |||||||
chr14:92722940 | A | G | 1 | a0001c0001t0001g0374 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.139-4096T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722940 | |||||||
chr14:92722958 | T | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(100): Show |
106 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.139-4114A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722958 | |||||||
chr14:92722977 | G | A | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4133C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92722977 | |||||||
chr14:92723049 | A | AT | 14 | a0001c0001t0001g0060 a0001c0001t0001g0157 a0001c0001t0001g0194 others(11): Show |
14 | HG00597.hp2 HG02145.hp2 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-4206dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723049 | |||||||
chr14:92723049 | A | ATC | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4206_139-4205i others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723049 | |||||||
chr14:92723069 | C | T | 2 | a0001c0001t0005g0116 a0002c0003t0005g0040 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.139-4225G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723069 | |||||||
chr14:92723070 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4226T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723070 | |||||||
chr14:92723078 | G | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4234C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723078 | |||||||
chr14:92723079 | T | C | 329 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(326): Show |
338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.139-4235A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723079 | |||||||
chr14:92723085 | C | T | 1 | a0002c0003t0001g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.139-4241G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723085 | |||||||
chr14:92723086 | G | A | 3 | a0001c0001t0001g0042 a0001c0002t0001g0094 a0001c0002t0001g0096 |
3 | HG02615.hp2 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.139-4242C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723086 | |||||||
chr14:92723115 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0032 a0002c0003t0002g0153 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4271G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723115 | |||||||
chr14:92723158 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4314A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723158 | |||||||
chr14:92723203 | C | T | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-4359G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723203 | |||||||
chr14:92723204 | A | G | 330 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(327): Show |
339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.139-4360T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723204 | |||||||
chr14:92723324 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(110): Show |
116 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.139-4480A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723324 | |||||||
chr14:92723337 | A | G | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4493T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723337 | |||||||
chr14:92723338 | T | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4494A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723338 | |||||||
chr14:92723351 | T | C | 9 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-4507A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723351 | |||||||
chr14:92723368 | T | C | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.139-4524A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723368 | |||||||
chr14:92723451 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.139-4607A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723451 | |||||||
chr14:92723519 | A | G | 33 | a0001c0001t0001g0157 a0001c0004t0001g0021 a0001c0004t0001g0022 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.139-4675T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723519 | |||||||
chr14:92723523 | C | T | 1 | a0001c0004t0001g0252 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.139-4679G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723523 | |||||||
chr14:92723591 | C | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(4): Show |
7 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-4747G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723591 | |||||||
chr14:92723703 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4859T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723703 | |||||||
chr14:92723736 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
148 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.139-4892G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723736 | |||||||
chr14:92723739 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4895G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723739 | |||||||
chr14:92723739 | CT | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
148 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.139-4896delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723739 | |||||||
chr14:92723813 | C | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-4969G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723813 | |||||||
chr14:92723834 | C | T | 1 | a0002c0003t0001g0110 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.139-4990G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723834 | |||||||
chr14:92723845 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.139-5001T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723845 | |||||||
chr14:92723978 | C | T | 3 | a0002c0005t0001g0030 a0002c0005t0001g0112 a0002c0005t0001g0113 |
3 | HG02572.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.139-5134G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723978 | |||||||
chr14:92723987 | T | C | 1 | a0001c0001t0005g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.139-5143A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92723987 | |||||||
chr14:92724004 | T | C | 2 | a0001c0008t0001g0043 a0002c0003t0006g0185 |
2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.139-5160A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724004 | |||||||
chr14:92724124 | A | G | 19 | a0001c0001t0001g0048 a0001c0001t0001g0115 a0001c0001t0001g0118 others(16): Show |
19 | HG00733.hp1 HG01106.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.139-5280T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724124 | |||||||
chr14:92724160 | T | C | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(268): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.139-5316A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724160 | |||||||
chr14:92724228 | T | C | 21 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0117 others(18): Show |
21 | HG01891.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.139-5384A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724228 | |||||||
chr14:92724393 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.139-5549A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724393 | |||||||
chr14:92724438 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(58): Show |
63 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.139-5594C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724438 | |||||||
chr14:92724554 | G | A | 16 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0119 others(13): Show |
16 | HG00733.hp1 HG01106.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.139-5710C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724554 | |||||||
chr14:92724648 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.139-5804C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724648 | |||||||
chr14:92724668 | A | G | 320 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(317): Show |
327 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.139-5824T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724668 | |||||||
chr14:92724739 | G | A | 5 | a0001c0001t0001g0327 a0001c0002t0001g0195 a0001c0002t0001g0326 others(2): Show |
5 | HG01123.hp2 HG01934.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-5895C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92724739 | |||||||
chr14:92725126 | T | G | 290 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(287): Show |
297 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.139-6282A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725126 | |||||||
chr14:92725153 | G | A | 1 | a0002c0003t0001g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.139-6309C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725153 | |||||||
chr14:92725160 | C | A | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139-6316G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725160 | |||||||
chr14:92725497 | T | C | 3 | a0001c0001t0001g0038 a0001c0002t0001g0094 a0001c0002t0001g0096 |
3 | HG02615.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.139-6653A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725497 | |||||||
chr14:92725507 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0090 a0001c0001t0005g0116 others(1): Show |
4 | HG01192.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.139-6663C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725507 | |||||||
chr14:92725538 | T | C | 282 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(279): Show |
289 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(286): Show |
intron_variant | MODIFIER | c.139-6694A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725538 | |||||||
chr14:92725597 | A | G | 1 | a0001c0002t0001g0168 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.139-6753T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725597 | |||||||
chr14:92725795 | A | T | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.138+6854T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725795 | |||||||
chr14:92725876 | C | T | 1 | a0002c0003t0001g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.138+6773G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725876 | |||||||
chr14:92725877 | G | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(37): Show |
42 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.138+6772C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92725877 | |||||||
chr14:92726097 | C | T | 1 | a0002c0003t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138+6552G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726097 | |||||||
chr14:92726169 | G | A | 11 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0118 others(8): Show |
11 | HG00733.hp1 HG01106.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.138+6480C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726169 | |||||||
chr14:92726194 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0103 others(3): Show |
6 | HG02145.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+6455C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726194 | |||||||
chr14:92726237 | C | CA | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
77 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.138+6411dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726237 | |||||||
chr14:92726237 | CA | C | 9 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(6): Show |
9 | HG03017.hp2 NA18942.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+6411delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726237 | |||||||
chr14:92726344 | G | A | 24 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0118 others(21): Show |
24 | HG00733.hp1 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.138+6305C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726344 | |||||||
chr14:92726355 | C | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0126 a0001c0017t0001g0095 |
3 | HG02486.hp1 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.138+6294G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726355 | |||||||
chr14:92726661 | C | T | 1 | a0001c0004t0001g0022 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.138+5988G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726661 | |||||||
chr14:92726690 | C | T | 13 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(10): Show |
13 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+5959G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726690 | |||||||
chr14:92726725 | C | T | 95 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(92): Show |
96 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.138+5924G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726725 | |||||||
chr14:92726871 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138+5778A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726871 | |||||||
chr14:92726981 | T | A | 1 | a0001c0002t0001g0285 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.138+5668A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92726981 | |||||||
chr14:92727045 | G | T | 1 | a0002c0003t0001g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.138+5604C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727045 | |||||||
chr14:92727192 | A | AG | 335 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(332): Show |
344 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.138+5456dupC | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727192 | |||||||
chr14:92727200 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(187): Show |
196 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.138+5449G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727200 | |||||||
chr14:92727201 | G | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0393 |
2 | HG02056.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.138+5448C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727201 | |||||||
chr14:92727258 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.138+5391G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727258 | |||||||
chr14:92727373 | T | C | 3 | a0001c0002t0001g0391 a0001c0002t0001g0392 a0001c0002t0001g0401 |
3 | HG00140.hp2 HG01361.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.138+5276A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727373 | |||||||
chr14:92727429 | C | CA | 110 | a0001c0001t0001g0009 a0001c0001t0001g0046 a0001c0001t0001g0050 others(107): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.138+5219dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727429 | |||||||
chr14:92727429 | C | CAA | 26 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0108 others(23): Show |
26 | HG00408.hp1 HG00597.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.138+5218_138+5219d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727429 | |||||||
chr14:92727560 | A | G | 2 | a0002c0003t0001g0307 a0002c0003t0001g0308 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.138+5089T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727560 | |||||||
chr14:92727567 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.138+5082C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727567 | |||||||
chr14:92727577 | C | T | 1 | a0002c0003t0001g0078 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.138+5072G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727577 | |||||||
chr14:92727677 | C | T | 3 | a0001c0001t0001g0127 a0006c0011t0001g0013 a0006c0011t0001g0014 |
3 | HG02683.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.138+4972G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727677 | |||||||
chr14:92727750 | G | A | 2 | a0001c0001t0001g0042 a0001c0017t0001g0095 |
2 | HG02486.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.138+4899C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727750 | |||||||
chr14:92727878 | A | ACACCCCT others(8): Show |
1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.138+4756_138+4770d others(17): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727878 | |||||||
chr14:92727971 | G | A | 3 | a0001c0001t0001g0229 a0005c0010t0003g0027 a0005c0010t0003g0093 |
3 | HG01358.hp1 HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.138+4678C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727971 | |||||||
chr14:92727981 | C | T | 352 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(349): Show |
361 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(358): Show |
intron_variant | MODIFIER | c.138+4668G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92727981 | |||||||
chr14:92728297 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.138+4352G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728297 | |||||||
chr14:92728342 | T | C | 3 | a0002c0003t0001g0110 a0002c0005t0001g0112 a0002c0005t0001g0113 |
3 | HG02572.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.138+4307A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728342 | |||||||
chr14:92728374 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0102 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.138+4275A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728374 | |||||||
chr14:92728426 | G | A | 1 | a0001c0002t0002g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138+4223C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728426 | |||||||
chr14:92728771 | T | C | 1 | a0001c0001t0005g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.138+3878A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728771 | |||||||
chr14:92728841 | C | T | 301 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(298): Show |
308 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.138+3808G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728841 | |||||||
chr14:92728849 | C | G | 1 | a0001c0001t0001g0336 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.138+3800G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92728849 | |||||||
chr14:92729029 | C | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(179): Show |
186 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.138+3620G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729029 | |||||||
chr14:92729122 | CTTTTCTT others(9): Show |
C | 4 | a0001c0001t0001g0369 a0001c0001t0002g0024 a0001c0002t0002g0367 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+3511_138+3526d others(18): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729122 | |||||||
chr14:92729127 | C | CT | 28 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0045 others(25): Show |
28 | HG00621.hp1 HG00733.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.138+3521dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729127 | |||||||
chr14:92729127 | CT | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0046 others(54): Show |
58 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.138+3521delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729127 | |||||||
chr14:92729133 | T | C | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.138+3516A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729133 | |||||||
chr14:92729211 | T | C | 1 | a0001c0001t0001g0302 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.138+3438A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729211 | |||||||
chr14:92729217 | T | C | 76 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(73): Show |
77 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.138+3432A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729217 | |||||||
chr14:92729467 | G | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0056 |
2 | HG02132.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.138+3182C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GC | 52 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0026 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.138+3181dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCC | 56 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(53): Show |
57 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.138+3180_138+3181d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCC | 46 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0061 others(43): Show |
48 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.138+3179_138+3181d others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCCC | 27 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0062 others(24): Show |
27 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.138+3178_138+3181d others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCCCC | 28 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0060 others(25): Show |
28 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.138+3177_138+3181d others(7): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCCCCCC | 30 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0126 others(27): Show |
32 | HG00544.hp2 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.138+3175_138+3181d others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCCCCCC others(3): Show |
9 | a0001c0001t0001g0038 a0001c0001t0002g0032 a0001c0002t0001g0094 others(6): Show |
9 | HG01123.hp1 HG01361.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.138+3172_138+3181d others(12): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729467 | G | GCCCCCCC others(4): Show |
1 | a0002c0003t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.138+3171_138+3181d others(13): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729467 | |||||||
chr14:92729475 | C | CCCG | 27 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0143 others(24): Show |
28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.138+3173_138+3174i others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729475 | |||||||
chr14:92729475 | C | CCG | 61 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0020 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.138+3173_138+3174i others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729475 | |||||||
chr14:92729475 | C | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138+3174G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729475 | |||||||
chr14:92729607 | C | G | 1 | a0001c0001t0001g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.138+3042G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729607 | |||||||
chr14:92729643 | G | A | 2 | a0001c0014t0001g0033 a0001c0014t0001g0047 |
2 | HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.138+3006C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92729643 | |||||||
chr14:92730242 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.138+2407A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730242 | |||||||
chr14:92730446 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138+2203G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730446 | |||||||
chr14:92730489 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.138+2160G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730489 | |||||||
chr14:92730772 | G | A | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.138+1877C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730772 | |||||||
chr14:92730774 | C | T | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(347): Show |
359 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.138+1875G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730774 | |||||||
chr14:92730886 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.138+1763G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730886 | |||||||
chr14:92730895 | A | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | NA18994.hp2 NA19000.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.138+1754T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730895 | |||||||
chr14:92730933 | CAAAAAAA | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.138+1709_138+1715d others(9): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730933 | |||||||
chr14:92730947 | AAAG | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(82): Show |
86 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.138+1699_138+1701d others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92730947 | |||||||
chr14:92731085 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(86): Show |
92 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.138+1564C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731085 | |||||||
chr14:92731132 | G | A | 3 | a0001c0001t0001g0127 a0006c0011t0001g0013 a0006c0011t0001g0014 |
3 | HG02683.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.138+1517C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731132 | |||||||
chr14:92731228 | T | C | 4 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0008t0001g0034 others(1): Show |
4 | HG02451.hp2 HG02486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+1421A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731228 | |||||||
chr14:92731338 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.138+1311A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731338 | |||||||
chr14:92731566 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.138+1083A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731566 | |||||||
chr14:92731812 | T | G | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138+837A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731812 | |||||||
chr14:92731818 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01074.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.138+831G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731818 | |||||||
chr14:92731939 | C | T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
51 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.138+710G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731939 | |||||||
chr14:92731999 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+650C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92731999 | |||||||
chr14:92732039 | CAG | C | 6 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0103 others(3): Show |
6 | HG02145.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+608_138+609del others(2): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732039 | |||||||
chr14:92732043 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.138+606C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732043 | |||||||
chr14:92732044 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.138+605T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732044 | |||||||
chr14:92732047 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0364 |
2 | NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.138+602G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732047 | |||||||
chr14:92732206 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.138+443G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732206 | |||||||
chr14:92732224 | C | T | 1 | a0001c0002t0001g0401 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.138+425G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732224 | |||||||
chr14:92732225 | G | A | 2 | a0001c0001t0001g0369 a0001c0002t0002g0368 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.138+424C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732225 | |||||||
chr14:92732539 | C | A | 1 | a0001c0004t0001g0252 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.138+110G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732539 | |||||||
chr14:92732567 | T | C | 3 | a0001c0001t0001g0382 a0001c0001t0001g0383 a0004c0013t0001g0384 |
3 | HG00741.hp1 HG01099.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.138+82A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732567 | |||||||
chr14:92732627 | A | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.138+22T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 2/13 | chr14 | 92732627 | |||||||
chr14:92732858 | T | A | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
358 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.-29-43A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92732858 | |||||||
chr14:92732877 | G | A | 3 | a0002c0003t0001g0081 a0002c0003t0001g0082 a0002c0003t0001g0083 |
3 | NA18965.hp1 NA19009.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-29-62C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92732877 | |||||||
chr14:92733023 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-29-208G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733023 | |||||||
chr14:92733092 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-29-277A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733092 | |||||||
chr14:92733099 | G | C | 1 | a0006c0011t0001g0013 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-29-284C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733099 | |||||||
chr14:92733148 | CA | C | 336 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(333): Show |
345 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(342): Show |
intron_variant | MODIFIER | c.-29-334delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733148 | |||||||
chr14:92733344 | G | A | 3 | a0001c0001t0001g0038 a0001c0002t0001g0094 a0001c0002t0001g0096 |
3 | HG02615.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-29-529C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733344 | |||||||
chr14:92733386 | C | A | 3 | a0001c0002t0001g0363 a0001c0004t0001g0253 a0001c0004t0001g0378 |
3 | HG01256.hp2 HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-29-571G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733386 | |||||||
chr14:92733413 | G | A | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29-598C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733413 | |||||||
chr14:92733413 | G | GT | 9 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0144 others(6): Show |
9 | HG01168.hp2 HG02738.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-599dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733413 | |||||||
chr14:92733507 | T | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0344 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-29-692A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733507 | |||||||
chr14:92733523 | T | A | 1 | a0001c0014t0001g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-29-708A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733523 | |||||||
chr14:92733720 | T | A | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-905A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733720 | |||||||
chr14:92733750 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-29-935A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733750 | |||||||
chr14:92733803 | G | T | 299 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(296): Show |
306 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-29-988C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733803 | |||||||
chr14:92733856 | A | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-1041T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92733856 | |||||||
chr14:92734022 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0221 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-29-1207A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734022 | |||||||
chr14:92734159 | A | C | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29-1344T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734159 | |||||||
chr14:92734169 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-29-1354A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734169 | |||||||
chr14:92734206 | CT | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-29-1392delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734206 | |||||||
chr14:92734254 | G | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0018 others(38): Show |
43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-29-1439C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734254 | |||||||
chr14:92734278 | G | A | 4 | a0001c0001t0001g0369 a0001c0001t0002g0024 a0001c0002t0002g0367 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1463C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734278 | |||||||
chr14:92734464 | A | G | 93 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0050 others(90): Show |
94 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-29-1649T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734464 | |||||||
chr14:92734646 | G | GA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0167 a0001c0001t0001g0210 others(3): Show |
6 | NA18967.hp1 NA19000.hp1 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-1832dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734646 | |||||||
chr14:92734646 | GA | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(88): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-29-1832delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734646 | |||||||
chr14:92734695 | A | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-1880T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734695 | |||||||
chr14:92734784 | T | C | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(347): Show |
359 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.-29-1969A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734784 | |||||||
chr14:92734824 | A | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-29-2009T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734824 | |||||||
chr14:92734953 | G | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0114 a0001c0001t0001g0399 |
3 | HG02280.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-29-2138C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92734953 | |||||||
chr14:92735098 | G | GTC | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(347): Show |
359 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.-29-2285_-29-2284d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735098 | |||||||
chr14:92735388 | G | C | 2 | a0001c0002t0001g0094 a0001c0002t0001g0096 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-29-2573C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735388 | |||||||
chr14:92735397 | G | T | 3 | a0001c0001t0001g0388 a0001c0001t0001g0404 a0001c0002t0001g0406 |
3 | HG00733.hp2 HG00738.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-29-2582C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735397 | |||||||
chr14:92735497 | G | A | 4 | a0001c0001t0001g0127 a0001c0004t0001g0159 a0006c0011t0001g0013 others(1): Show |
4 | HG02027.hp2 HG02683.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-2682C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735497 | |||||||
chr14:92735508 | TGAGACTG others(17): Show |
T | 1 | a0001c0001t0001g0245 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-29-2717_-29-2694d others(26): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735508 | |||||||
chr14:92735654 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(286): Show |
296 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.-29-2839G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735654 | |||||||
chr14:92735677 | G | A | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(345): Show |
357 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(354): Show |
intron_variant | MODIFIER | c.-29-2862C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735677 | |||||||
chr14:92735683 | T | C | 162 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0038 others(159): Show |
166 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(163): Show |
intron_variant | MODIFIER | c.-29-2868A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735683 | |||||||
chr14:92735790 | T | G | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-29-2975A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735790 | |||||||
chr14:92735803 | GT | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0117 others(14): Show |
17 | HG01192.hp2 HG02451.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-29-2989delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735803 | |||||||
chr14:92735866 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0103 others(9): Show |
12 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-3051C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735866 | |||||||
chr14:92735870 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0103 others(16): Show |
19 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-29-3055G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735870 | |||||||
chr14:92735877 | T | G | 17 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0103 others(14): Show |
17 | HG01109.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-3062A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735877 | |||||||
chr14:92735946 | G | C | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29-3131C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92735946 | |||||||
chr14:92736043 | C | T | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-29-3228G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736043 | |||||||
chr14:92736400 | G | A | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0002c0003t0001g0074 others(2): Show |
5 | HG02155.hp2 NA18959.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-3585C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736400 | |||||||
chr14:92736447 | T | G | 6 | a0001c0001t0001g0097 a0001c0001t0002g0187 a0001c0001t0002g0188 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3632A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736447 | |||||||
chr14:92736456 | C | T | 1 | a0002c0006t0001g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-29-3641G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736456 | |||||||
chr14:92736521 | G | A | 15 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(12): Show |
15 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29-3706C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736521 | |||||||
chr14:92736587 | C | A | 1 | a0002c0003t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-29-3772G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736587 | |||||||
chr14:92736613 | A | G | 95 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(92): Show |
97 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-29-3798T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736613 | |||||||
chr14:92736659 | T | C | 2 | a0001c0001t0001g0183 a0002c0003t0001g0092 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29-3844A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736659 | |||||||
chr14:92736764 | C | A | 1 | a0002c0005t0001g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-29-3949G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92736764 | |||||||
chr14:92737060 | G | A | 2 | a0001c0001t0001g0090 a0001c0002t0001g0091 |
2 | HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-29-4245C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737060 | |||||||
chr14:92737215 | A | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0102 others(18): Show |
21 | HG00733.hp1 HG01106.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.-29-4400T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737215 | |||||||
chr14:92737242 | C | T | 15 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(12): Show |
15 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.-29-4427G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737242 | |||||||
chr14:92737304 | C | T | 5 | a0001c0001t0001g0369 a0001c0001t0002g0024 a0001c0002t0002g0367 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-4489G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737304 | |||||||
chr14:92737327 | AG | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0167 a0001c0001t0001g0337 others(4): Show |
7 | HG01993.hp1 NA18947.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-4513delC | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737327 | |||||||
chr14:92737381 | A | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0115 others(4): Show |
7 | HG00733.hp1 HG01106.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-4566T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737381 | |||||||
chr14:92737464 | T | C | 2 | a0001c0001t0001g0097 a0002c0005t0001g0122 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-29-4649A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737464 | |||||||
chr14:92737785 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29-4970T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92737785 | |||||||
chr14:92738313 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0045 others(46): Show |
50 | HG00280.hp2 HG00438.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.-29-5498G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738313 | |||||||
chr14:92738399 | C | G | 7 | a0001c0001t0001g0048 a0001c0014t0001g0047 a0002c0003t0001g0120 others(4): Show |
7 | HG02451.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-29-5584G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738399 | |||||||
chr14:92738399 | C | T | 5 | a0001c0001t0001g0369 a0001c0001t0002g0024 a0001c0002t0002g0367 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-5584G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738399 | |||||||
chr14:92738425 | C | A | 1 | a0001c0001t0001g0351 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-29-5610G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738425 | |||||||
chr14:92738635 | T | C | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | NA18942.hp1 NA18986.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-5820A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738635 | |||||||
chr14:92738651 | G | A | 5 | a0001c0001t0001g0369 a0001c0001t0002g0024 a0001c0002t0002g0367 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-5836C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738651 | |||||||
chr14:92738786 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0167 |
2 | NA18988.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-29-5971G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738786 | |||||||
chr14:92738809 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-29-5994T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738809 | |||||||
chr14:92738880 | G | A | 3 | a0001c0001t0001g0369 a0001c0002t0002g0367 a0001c0002t0002g0368 |
3 | HG02572.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-29-6065C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92738880 | |||||||
chr14:92739017 | C | CA | 25 | a0001c0001t0001g0136 a0001c0001t0001g0180 a0001c0001t0001g0194 others(22): Show |
25 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-29-6203dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739017 | |||||||
chr14:92739031 | AC | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0140 |
3 | NA18942.hp1 NA18998.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-29-6217delG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739031 | |||||||
chr14:92739032 | C | A | 16 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0127 others(13): Show |
16 | HG01981.hp2 HG02683.hp1 HG02735.hp2 others(13): Show |
intron_variant | MODIFIER | c.-29-6217G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739032 | |||||||
chr14:92739040 | A | C | 1 | a0001c0001t0001g0238 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-29-6225T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739040 | |||||||
chr14:92739265 | C | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0115 others(4): Show |
7 | HG00733.hp1 HG01106.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-6450G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739265 | |||||||
chr14:92739309 | C | T | 5 | a0002c0003t0001g0120 a0002c0003t0001g0121 a0002c0003t0006g0185 others(2): Show |
5 | HG02818.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-6494G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739309 | |||||||
chr14:92739471 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0103 |
2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-29-6656C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739471 | |||||||
chr14:92739527 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0002g0187 a0001c0001t0002g0188 others(1): Show |
4 | HG01884.hp2 HG02486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-6712T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739527 | |||||||
chr14:92739889 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-29-7074G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739889 | |||||||
chr14:92739890 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-29-7075C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92739890 | |||||||
chr14:92740108 | C | T | 2 | a0001c0008t0001g0034 a0001c0008t0001g0044 |
2 | HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-29-7293G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740108 | |||||||
chr14:92740203 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-29-7388C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740203 | |||||||
chr14:92740218 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(111): Show |
117 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.-29-7403T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740218 | |||||||
chr14:92740230 | A | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0102 a0001c0001t0001g0115 others(4): Show |
7 | HG00733.hp1 HG01106.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-7415T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740230 | |||||||
chr14:92740243 | C | T | 13 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG03017.hp2 HG03710.hp1 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-7428G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740243 | |||||||
chr14:92740252 | AAAAG | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | NA18942.hp1 NA18986.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-7441_-29-7438d others(6): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740252 | |||||||
chr14:92740263 | A | G | 1 | a0002c0003t0001g0035 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-29-7448T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740263 | |||||||
chr14:92740672 | T | C | 4 | a0002c0003t0001g0029 a0002c0003t0001g0191 a0002c0005t0001g0030 others(1): Show |
4 | HG01255.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+7817A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740672 | |||||||
chr14:92740909 | G | A | 1 | a0001c0004t0001g0360 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-30+7580C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740909 | |||||||
chr14:92740918 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-30+7571C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740918 | |||||||
chr14:92740956 | A | G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(126): Show |
132 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-30+7533T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740956 | |||||||
chr14:92740960 | G | T | 83 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(80): Show |
85 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-30+7529C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740960 | |||||||
chr14:92740973 | C | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(99): Show |
105 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.-30+7516G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740973 | |||||||
chr14:92740985 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0183 a0002c0003t0001g0092 others(1): Show |
4 | HG02055.hp1 HG03540.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+7504C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92740985 | |||||||
chr14:92741196 | A | G | 16 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(13): Show |
16 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(13): Show |
intron_variant | MODIFIER | c.-30+7293T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741196 | |||||||
chr14:92741317 | A | G | 2 | a0005c0010t0003g0027 a0005c0010t0003g0093 |
2 | HG02258.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-30+7172T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741317 | |||||||
chr14:92741409 | C | A | 3 | a0001c0001t0001g0369 a0001c0002t0002g0367 a0001c0002t0002g0368 |
3 | HG02572.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-30+7080G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741409 | |||||||
chr14:92741435 | G | A | 2 | a0001c0001t0001g0090 a0001c0002t0001g0091 |
2 | HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+7054C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741435 | |||||||
chr14:92741578 | C | G | 1 | a0001c0004t0001g0353 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-30+6911G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741578 | |||||||
chr14:92741579 | G | C | 1 | a0001c0004t0001g0353 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-30+6910C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741579 | |||||||
chr14:92741625 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-30+6864G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741625 | |||||||
chr14:92741686 | C | A | 1 | a0001c0001t0001g0349 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-30+6803G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741686 | |||||||
chr14:92741887 | A | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-30+6602T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741887 | |||||||
chr14:92741955 | C | T | 1 | a0002c0003t0001g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-30+6534G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92741955 | |||||||
chr14:92742049 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0126 |
2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-30+6440C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742049 | |||||||
chr14:92742138 | T | A | 1 | a0002c0003t0001g0148 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+6351A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742138 | |||||||
chr14:92742156 | A | AC | 40 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0238 others(37): Show |
41 | HG00280.hp2 HG00438.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-30+6332dupG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742156 | |||||||
chr14:92742246 | C | T | 1 | a0001c0004t0001g0376 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-30+6243G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742246 | |||||||
chr14:92742285 | T | A | 1 | a0002c0003t0001g0350 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-30+6204A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742285 | |||||||
chr14:92742292 | C | CT | 24 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0221 others(21): Show |
24 | HG01074.hp1 HG01106.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-30+6196dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742292 | |||||||
chr14:92742303 | TTTC | T | 51 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(48): Show |
53 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.-30+6183_-30+6185d others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742303 | |||||||
chr14:92742304 | TTC | T | 11 | a0001c0001t0001g0157 a0001c0001t0001g0170 a0001c0001t0001g0174 others(8): Show |
11 | HG01257.hp2 HG02738.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30+6183_-30+6184d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742304 | |||||||
chr14:92742305 | TC | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0016 others(96): Show |
101 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-30+6183delG | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742305 | |||||||
chr14:92742306 | C | T | 241 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(238): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-30+6183G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742306 | |||||||
chr14:92742337 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0403 |
2 | HG00621.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-30+6152C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742337 | |||||||
chr14:92742354 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-30+6135T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742354 | |||||||
chr14:92742393 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-30+6096C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742393 | |||||||
chr14:92742476 | T | C | 1 | a0002c0003t0001g0361 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30+6013A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742476 | |||||||
chr14:92742498 | G | A | 18 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(15): Show |
18 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(15): Show |
intron_variant | MODIFIER | c.-30+5991C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742498 | |||||||
chr14:92742507 | G | A | 1 | a0001c0001t0001g0404 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-30+5982C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742507 | |||||||
chr14:92742528 | G | A | 18 | a0001c0001t0001g0127 a0001c0001t0001g0131 a0001c0001t0001g0132 others(15): Show |
18 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(15): Show |
intron_variant | MODIFIER | c.-30+5961C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742528 | |||||||
chr14:92742647 | G | C | 1 | a0001c0001t0001g0351 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-30+5842C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742647 | |||||||
chr14:92742661 | T | C | 49 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0020 others(46): Show |
51 | HG01168.hp2 HG01243.hp1 HG01257.hp2 others(48): Show |
intron_variant | MODIFIER | c.-30+5828A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742661 | |||||||
chr14:92742837 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-30+5652A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92742837 | |||||||
chr14:92743024 | C | CA | 48 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0048 others(45): Show |
48 | HG00423.hp1 HG00735.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-30+5464dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743024 | |||||||
chr14:92743024 | CA | C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0183 a0001c0001t0001g0377 others(4): Show |
7 | HG01257.hp2 HG01884.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+5464delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743024 | |||||||
chr14:92743114 | C | T | 1 | a0002c0003t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-30+5375G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743114 | |||||||
chr14:92743411 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30+5078C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743411 | |||||||
chr14:92743427 | C | T | 2 | a0001c0002t0001g0217 a0001c0002t0001g0218 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-30+5062G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743427 | |||||||
chr14:92743502 | C | CA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0125 a0001c0001t0001g0183 others(5): Show |
8 | HG00597.hp2 HG01981.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30+4986dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743502 | |||||||
chr14:92743522 | C | A | 3 | a0001c0001t0001g0369 a0001c0002t0002g0367 a0001c0002t0002g0368 |
3 | HG02572.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-30+4967G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743522 | |||||||
chr14:92743539 | C | T | 3 | a0001c0001t0001g0369 a0001c0002t0002g0367 a0001c0002t0002g0368 |
3 | HG02572.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-30+4950G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743539 | |||||||
chr14:92743550 | C | T | 1 | a0001c0004t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-30+4939G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743550 | |||||||
chr14:92743617 | C | A | 2 | a0001c0001t0001g0048 a0001c0014t0001g0047 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-30+4872G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743617 | |||||||
chr14:92743621 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0002g0024 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-30+4868G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743621 | |||||||
chr14:92743622 | G | A | 2 | a0001c0001t0002g0187 a0001c0001t0002g0188 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-30+4867C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743622 | |||||||
chr14:92743630 | A | G | 43 | a0001c0001t0001g0018 a0001c0001t0001g0090 a0001c0001t0001g0097 others(40): Show |
43 | HG00733.hp1 HG01106.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.-30+4859T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743630 | |||||||
chr14:92743801 | C | CA | 9 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0362 others(6): Show |
9 | HG01433.hp1 HG02293.hp1 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.-30+4687dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743801 | |||||||
chr14:92743801 | CA | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(48): Show |
52 | HG00642.hp1 HG00733.hp1 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.-30+4687delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743801 | |||||||
chr14:92743801 | CAA | C | 20 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0131 others(17): Show |
20 | HG02683.hp1 HG03017.hp2 HG03688.hp1 others(17): Show |
intron_variant | MODIFIER | c.-30+4686_-30+4687d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743801 | |||||||
chr14:92743921 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
120 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.-30+4568A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743921 | |||||||
chr14:92743922 | G | A | 5 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0002c0003t0006g0185 others(2): Show |
5 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+4567C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743922 | |||||||
chr14:92743931 | G | A | 1 | a0002c0003t0001g0011 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-30+4558C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743931 | |||||||
chr14:92743965 | C | A | 2 | a0001c0001t0001g0097 a0002c0005t0001g0122 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-30+4524G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743965 | |||||||
chr14:92743982 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-30+4507G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92743982 | |||||||
chr14:92744047 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
21 | HG00642.hp1 HG01109.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30+4442C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744047 | |||||||
chr14:92744111 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-30+4378C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744111 | |||||||
chr14:92744144 | T | C | 3 | a0001c0001t0001g0369 a0001c0002t0002g0367 a0001c0002t0002g0368 |
3 | HG02572.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-30+4345A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744144 | |||||||
chr14:92744175 | A | G | 1 | a0001c0001t0007g0215 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-30+4314T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744175 | |||||||
chr14:92744199 | C | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
109 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.-30+4290G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744199 | |||||||
chr14:92744278 | G | T | 1 | a0001c0001t0001g0206 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-30+4211C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744278 | |||||||
chr14:92744461 | T | G | 5 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0002c0003t0006g0185 others(2): Show |
5 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30+4028A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744461 | |||||||
chr14:92744478 | G | A | 2 | a0001c0001t0001g0370 a0001c0001t0001g0371 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-30+4011C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744478 | |||||||
chr14:92744594 | G | GT | 26 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0090 others(23): Show |
26 | HG00733.hp1 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30+3894dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744594 | |||||||
chr14:92744594 | GT | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0052 others(48): Show |
53 | HG00323.hp2 HG00544.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-30+3894delA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744594 | |||||||
chr14:92744786 | G | A | 2 | a0001c0001t0001g0097 a0002c0005t0001g0122 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-30+3703C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744786 | |||||||
chr14:92744830 | G | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0002t0001g0207 |
3 | HG00438.hp1 NA18982.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-30+3659C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744830 | |||||||
chr14:92744836 | C | T | 1 | a0002c0005t0008g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30+3653G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744836 | |||||||
chr14:92744989 | G | A | 2 | a0001c0001t0001g0372 a0001c0019t0001g0373 |
2 | HG00609.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-30+3500C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92744989 | |||||||
chr14:92745055 | T | A | 2 | a0001c0001t0001g0090 a0001c0002t0001g0091 |
2 | HG01192.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-30+3434A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745055 | |||||||
chr14:92745064 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
25 | HG00642.hp1 HG01109.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-30+3425C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745064 | |||||||
chr14:92745116 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-30+3373T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745116 | |||||||
chr14:92745124 | C | T | 4 | a0001c0002t0001g0094 a0001c0002t0001g0096 a0001c0017t0001g0095 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+3365G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745124 | |||||||
chr14:92745280 | G | A | 1 | a0002c0003t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-30+3209C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745280 | |||||||
chr14:92745351 | C | T | 4 | a0002c0003t0002g0153 a0002c0003t0002g0154 a0002c0003t0002g0155 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+3138G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745351 | |||||||
chr14:92745611 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-30+2878G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745611 | |||||||
chr14:92745650 | C | A | 2 | a0002c0003t0001g0120 a0002c0003t0001g0121 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+2839G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745650 | |||||||
chr14:92745829 | C | CT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(79): Show |
84 | HG00099.hp2 HG00673.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.-30+2659dupA | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745829 | |||||||
chr14:92745835 | T | C | 3 | a0002c0003t0001g0191 a0002c0005t0001g0189 a0002c0009t0001g0190 |
3 | HG02559.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-30+2654A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745835 | |||||||
chr14:92745883 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30+2606C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745883 | |||||||
chr14:92745890 | C | T | 4 | a0001c0002t0001g0094 a0001c0002t0001g0096 a0001c0017t0001g0095 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+2599G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92745890 | |||||||
chr14:92746142 | G | A | 1 | a0001c0001t0001g0374 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30+2347C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746142 | |||||||
chr14:92746363 | T | TA | 6 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
6 | HG00733.hp1 HG01106.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+2125dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746363 | |||||||
chr14:92746428 | A | G | 1 | a0001c0002t0001g0202 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-30+2061T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746428 | |||||||
chr14:92746826 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1663C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746826 | |||||||
chr14:92746827 | C | G | 6 | a0001c0001t0001g0097 a0001c0002t0001g0094 a0001c0002t0001g0096 others(3): Show |
6 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+1662G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746827 | |||||||
chr14:92746828 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1661T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746828 | |||||||
chr14:92746829 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1660C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746829 | |||||||
chr14:92746830 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1659T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746830 | |||||||
chr14:92746833 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1656C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746833 | |||||||
chr14:92746835 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1654C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746835 | |||||||
chr14:92746837 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1652G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746837 | |||||||
chr14:92746840 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1649A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746840 | |||||||
chr14:92746850 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1639G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746850 | |||||||
chr14:92746855 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1634A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746855 | |||||||
chr14:92746865 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1624A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746865 | |||||||
chr14:92746866 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1623G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746866 | |||||||
chr14:92746867 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1622A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746867 | |||||||
chr14:92746868 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1621G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746868 | |||||||
chr14:92746869 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1620A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746869 | |||||||
chr14:92746871 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1618G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746871 | |||||||
chr14:92746872 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1617A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746872 | |||||||
chr14:92746876 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1613T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746876 | |||||||
chr14:92746878 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1611A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746878 | |||||||
chr14:92746880 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1609G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746880 | |||||||
chr14:92746883 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1606T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746883 | |||||||
chr14:92746885 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1604T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746885 | |||||||
chr14:92746887 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1602A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746887 | |||||||
chr14:92746891 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1598G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746891 | |||||||
chr14:92746892 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1597G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746892 | |||||||
chr14:92746893 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1596C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746893 | |||||||
chr14:92746894 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1595C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746894 | |||||||
chr14:92746900 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1589C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746900 | |||||||
chr14:92746902 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-30+1587C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746902 | |||||||
chr14:92746902 | G | T | 1 | a0002c0005t0008g0192 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-30+1587C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746902 | |||||||
chr14:92746906 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1583C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746906 | |||||||
chr14:92746907 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1582C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746907 | |||||||
chr14:92746909 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1580C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746909 | |||||||
chr14:92746910 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1579G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746910 | |||||||
chr14:92746911 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1578G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746911 | |||||||
chr14:92746916 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1573C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746916 | |||||||
chr14:92746917 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1572A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746917 | |||||||
chr14:92746918 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0183 |
2 | HG03017.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-30+1571G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746918 | |||||||
chr14:92746920 | T | C | 2 | a0002c0003t0001g0120 a0002c0003t0001g0121 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-30+1569A>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746920 | |||||||
chr14:92746921 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1568T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746921 | |||||||
chr14:92746922 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1567C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746922 | |||||||
chr14:92746924 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1565A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746924 | |||||||
chr14:92746929 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1560C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746929 | |||||||
chr14:92746935 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1554G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746935 | |||||||
chr14:92746936 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1553G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746936 | |||||||
chr14:92746941 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1548G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746941 | |||||||
chr14:92746950 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1539C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746950 | |||||||
chr14:92746951 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1538C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746951 | |||||||
chr14:92746952 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1537G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746952 | |||||||
chr14:92746953 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1536C>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746953 | |||||||
chr14:92746955 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1534C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746955 | |||||||
chr14:92746958 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1531G>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746958 | |||||||
chr14:92746960 | T | G | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1529A>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746960 | |||||||
chr14:92746961 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1528C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746961 | |||||||
chr14:92746963 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1526C>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746963 | |||||||
chr14:92746964 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-30+1525T>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92746964 | |||||||
chr14:92747035 | C | CA | 69 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0016 others(66): Show |
70 | HG00140.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-30+1453dupT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747035 | |||||||
chr14:92747035 | C | CAA | 34 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0126 others(31): Show |
35 | HG01109.hp1 HG01168.hp2 HG01358.hp2 others(32): Show |
intron_variant | MODIFIER | c.-30+1452_-30+1453d others(4): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747035 | |||||||
chr14:92747035 | C | CAAA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0152 others(32): Show |
37 | HG00099.hp2 HG01243.hp1 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.-30+1451_-30+1453d others(5): Show |
LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747035 | |||||||
chr14:92747035 | CA | C | 6 | a0001c0001t0001g0017 a0001c0002t0001g0195 a0001c0002t0001g0199 others(3): Show |
6 | HG01515.hp2 HG01928.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+1453delT | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747035 | |||||||
chr14:92747264 | C | T | 2 | a0001c0002t0001g0196 a0001c0002t0001g0197 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-30+1225G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747264 | |||||||
chr14:92747395 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG01891.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-30+1094G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747395 | |||||||
chr14:92747408 | T | A | 6 | a0001c0001t0001g0183 a0001c0001t0002g0187 a0001c0001t0002g0188 others(3): Show |
6 | HG02486.hp2 HG03041.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-30+1081A>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747408 | |||||||
chr14:92747446 | C | T | 3 | a0002c0003t0001g0191 a0002c0005t0001g0189 a0002c0009t0001g0190 |
3 | HG02559.hp1 HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-30+1043G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747446 | |||||||
chr14:92747633 | G | A | 4 | a0002c0003t0001g0191 a0002c0005t0001g0189 a0002c0005t0008g0192 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+856C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747633 | |||||||
chr14:92747860 | C | T | 2 | a0006c0011t0001g0013 a0006c0011t0001g0014 |
2 | HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-30+629G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747860 | |||||||
chr14:92747949 | C | A | 1 | a0001c0002t0001g0409 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30+540G>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92747949 | |||||||
chr14:92748069 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-30+420G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748069 | |||||||
chr14:92748071 | C | T | 2 | a0001c0001t0001g0194 a0001c0002t0001g0193 |
2 | HG00597.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-30+418G>A | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748071 | |||||||
chr14:92748224 | A | G | 3 | a0001c0002t0001g0010 a0002c0003t0001g0011 a0002c0005t0001g0012 |
3 | HG00639.hp1 HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-30+265T>C | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748224 | |||||||
chr14:92748228 | A | C | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.-30+261T>G | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748228 | |||||||
chr14:92748315 | G | A | 1 | a0002c0003t0001g0410 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-30+174C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748315 | |||||||
chr14:92748420 | G | A | 1 | a0002c0005t0001g0411 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-30+69C>T | LGMN | ENSG00000100600.15 | transcript | ENST00000334869.9 | protein_coding | 1/13 | chr14 | 92748420 |