Item | Value |
---|---|
geneid | 23367 |
ensemblid | ENSG00000155506.19 |
hgncid | 29531 |
symbol | LARP1 |
name | La ribonucleoprotein 1, translational regulator |
refseq_nuc | NM_033551.3 |
refseq_prot | NP_291029.2 |
ensembl_nuc | ENST00000518297.6 |
ensembl_prot | ENSP00000428589.2 |
mane_status | MANE Select |
chr | chr5 |
start | 154755377 |
end | 154817605 |
strand | + |
ver | v1.2 |
region | chr5:154755377-154817605 |
region5000 | chr5:154750377-154822605 |
regionname0 | LARP1_chr5_154755377_154817605 |
regionname5000 | LARP1_chr5_154750377_154822605 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1096 | 295 | 85 | 56 | 95 | 16 | 41 | 61 | LARP1_chr5_154750377_154822605 | LARP1 | MATQV others(1091): Show |
chr5 | 154750377 | 154822605 |
a0002 | 0/0 | 1096 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | MATQV others(1091): Show |
chr5 | 154750377 | 154822605 |
a0003 | 0/0 | 1096 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | MATQV others(1091): Show |
chr5 | 154750377 | 154822605 |
a0004 | 0/0 | 1096 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | MATQV others(1091): Show |
chr5 | 154750377 | 154822605 |
a0005 | 0/0 | 1096 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | MATQV others(1091): Show |
chr5 | 154750377 | 154822605 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3288 | 266 | 79 | 52 | 82 | 14 | 37 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0001c0002 | 0/0 | 3288 | 14 | 4 | 3 | 1 | 2 | 4 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0001c0003 | 0/0 | 3288 | 11 | 0 | 0 | 11 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0001c0006 | 0/0 | 3288 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0001c0008 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0001c0010 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0002c0004 | 0/0 | 3288 | 5 | 5 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0003c0005 | 0/0 | 3288 | 2 | 0 | 1 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0004c0009 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 | ||
a0005c0007 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | ATGGC others(3283): Show |
chr5 | 154750377 | 154822605 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7181 | 185 | 40 | 37 | 63 | 14 | 30 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0002 | 0/0 | 7182 | 12 | 0 | 0 | 8 | 0 | 4 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0003 | 0/0 | 7181 | 13 | 10 | 3 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0004 | 0/0 | 7180 | 10 | 9 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7175): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0005 | 0/0 | 7182 | 7 | 2 | 3 | 2 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0006 | 0/0 | 7182 | 7 | 7 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0007 | 0/0 | 7181 | 5 | 4 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0008 | 0/0 | 7181 | 4 | 2 | 2 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0009 | 0/0 | 7181 | 4 | 0 | 0 | 4 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0010 | 0/0 | 7181 | 3 | 0 | 2 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0011 | 0/0 | 7181 | 2 | 0 | 2 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0012 | 0/0 | 7183 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7178): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0013 | 0/0 | 7181 | 2 | 0 | 0 | 0 | 0 | 2 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0014 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0015 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0016 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0018 | 0/0 | 7181 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0019 | 0/1 | 7181 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0020 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0021 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0022 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0023 | 0/0 | 7183 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7178): Show |
chr5 | 154750377 | 154822605 |
a0001c0001t0024 | 0/0 | 7182 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0002t0001 | 0/0 | 7181 | 11 | 4 | 2 | 0 | 2 | 3 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0002t0002 | 0/0 | 7182 | 3 | 0 | 1 | 1 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0001c0003t0001 | 0/0 | 7181 | 11 | 0 | 0 | 11 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0006t0001 | 0/0 | 7181 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0008t0001 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0001c0010t0011 | 0/0 | 7181 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0002c0004t0001 | 0/0 | 7181 | 3 | 3 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0002c0004t0002 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0002c0004t0005 | 0/0 | 7182 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7177): Show |
chr5 | 154750377 | 154822605 |
a0003c0005t0001 | 0/0 | 7181 | 2 | 0 | 1 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0004c0009t0017 | 0/0 | 7181 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
a0005c0007t0001 | 0/0 | 7181 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | GTCCA others(7176): Show |
chr5 | 154750377 | 154822605 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0008g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0010g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0011g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0012g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0013g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0013g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0016g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0019g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0020g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0021g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0022g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0001t0024g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0008t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0001c0010t0011g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0002c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0002c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0002c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0002c0004t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0002c0004t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0003c0005t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0003c0005t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0004c0009t0017g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
a0005c0007t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00558 | hp1 | a0001 | c0001 | t0009 | g0138 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00609 | hp1 | a0001 | c0001 | t0014 | g0242 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00735 | hp2 | a0001 | c0001 | t0007 | g0071 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01109 | hp1 | a0004 | c0009 | t0017 | g0132 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01167 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0049 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01169 | hp1 | a0001 | c0001 | t0008 | g0031 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01175 | hp2 | a0001 | c0001 | t0010 | g0101 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0120 | AMR | PUR | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0100 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01346 | hp2 | a0001 | c0001 | t0011 | g0266 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0218 | EUR | IBS | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01934 | hp1 | a0003 | c0005 | t0001 | g0226 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01952 | hp2 | a0001 | c0001 | t0005 | g0113 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01993 | hp2 | a0001 | c0001 | t0024 | g0265 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0127 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0121 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02080 | hp2 | a0001 | c0001 | t0009 | g0139 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02129 | hp1 | a0001 | c0001 | t0009 | g0137 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0179 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02257 | hp1 | a0002 | c0004 | t0005 | g0004 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0040 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02280 | hp2 | a0002 | c0004 | t0001 | g0015 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02293 | hp1 | a0001 | c0010 | t0011 | g0280 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02300 | hp2 | a0001 | c0001 | t0011 | g0256 | AMR | PEL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0110 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0097 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0235 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0069 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02809 | hp1 | a0002 | c0004 | t0001 | g0016 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0133 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02886 | hp2 | a0001 | c0001 | t0016 | g0122 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0125 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0215 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0129 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02976 | hp2 | a0001 | c0001 | t0015 | g0124 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03041 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | GWD | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03130 | hp1 | a0002 | c0004 | t0002 | g0015 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0206 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0041 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03490 | hp2 | a0001 | c0001 | t0013 | g0079 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ESN | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0070 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03834 | hp2 | a0001 | c0001 | t0013 | g0064 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04204 | hp1 | a0001 | c0001 | t0010 | g0134 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04204 | hp2 | a0003 | c0005 | t0001 | g0225 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0131 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | CHB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18939 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18940 | hp1 | a0001 | c0001 | t0009 | g0136 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18945 | hp1 | a0001 | c0001 | t0022 | g0171 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18949 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18951 | hp2 | a0001 | c0001 | t0021 | g0186 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18954 | hp1 | a0001 | c0001 | t0020 | g0224 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18956 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18971 | hp2 | a0001 | c0008 | t0001 | g0230 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18975 | hp1 | a0001 | c0001 | t0023 | g0001 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18982 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18995 | hp2 | a0005 | c0007 | t0001 | g0175 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19075 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | TSI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | GIH | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | USA | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
HG06807 | hp2 | a0002 | c0004 | t0001 | g0259 | AFR | USA | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | USA | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | USA | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0223 | AFR | LWK | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
homoSapiens | chm13v2 | a0001 | c0001 | t0019 | g0003 | REF | REF | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | LARP1_chr5_154750377_154822605 | LARP1 | chr5 | 154750377 | 154822605 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154755872 | C | T | 1 | a0004 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.115C>T | p.Pro39Ser | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 496/7181 | 115/3291 | 39/1096 | chr5 | 154755872 | |||
chr5:154755914 | G | T | 1 | a0002 | 5 | HG02257.hp1 HG02280.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.157G>T | p.Ala53Ser | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 538/7181 | 157/3291 | 53/1096 | chr5 | 154755914 | |||
chr5:154756092 | G | A | 1 | a0003 | 2 | HG01934.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.335G>A | p.Gly112Glu | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 716/7181 | 335/3291 | 112/1096 | chr5 | 154756092 | |||
chr5:154808555 | A | G | 1 | a0005 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.2795A>G | p.Tyr932Cys | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/19 | 3176/7181 | 2795/3291 | 932/1096 | chr5 | 154808555 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154755811 | C | G | 1 | a0001c0010 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.54C>G | p.Ala18Ala | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 435/7181 | 54/3291 | 18/1096 | chr5 | 154755811 | |||
chr5:154755826 | G | A | 1 | a0001c0002 | 14 | HG00639.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
synonymous_variant | LOW | c.69G>A | p.Gly23Gly | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 450/7181 | 69/3291 | 23/1096 | chr5 | 154755826 | |||
chr5:154793710 | C | T | 1 | a0001c0006 | 2 | HG03041.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.855C>T | p.Arg285Arg | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 5/19 | 1236/7181 | 855/3291 | 285/1096 | chr5 | 154793710 | |||
chr5:154793825 | C | T | 1 | a0001c0008 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.894C>T | p.Pro298Pro | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 6/19 | 1275/7181 | 894/3291 | 298/1096 | chr5 | 154793825 | |||
chr5:154811250 | T | C | 1 | a0001c0003 | 11 | NA18747.hp1 NA18939.hp2 NA18949.hp1 others(8): Show |
synonymous_variant | LOW | c.2847T>C | p.Tyr949Tyr | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 17/19 | 3228/7181 | 2847/3291 | 949/1096 | chr5 | 154811250 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154755496 | C | CG | 5 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0024 others(2): Show |
18 | HG00558.hp2 HG00597.hp2 HG01175.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-254dupG | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 253 | INFO_REALIGN_3_PRIME | chr5 | 154755496 | |||||
chr5:154755546 | C | T | 1 | a0001c0001t0022 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 212 | chr5 | 154755546 | ||||||
chr5:154755632 | C | G | 1 | a0001c0001t0021 | 1 | NA18951.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 126 | chr5 | 154755632 | ||||||
chr5:154755728 | C | T | 1 | a0001c0001t0020 | 1 | NA18954.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/19 | 30 | chr5 | 154755728 | ||||||
chr5:154814261 | G | A | 1 | a0001c0001t0010 | 3 | HG01168.hp2 HG01175.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*165G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 165 | chr5 | 154814261 | ||||||
chr5:154814497 | C | G | 1 | a0001c0001t0018 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 401 | chr5 | 154814497 | ||||||
chr5:154814569 | G | T | 1 | a0001c0001t0009 | 4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*473G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 473 | chr5 | 154814569 | ||||||
chr5:154814607 | C | T | 1 | a0001c0001t0008 | 4 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*511C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 511 | chr5 | 154814607 | ||||||
chr5:154814707 | T | G | 1 | a0001c0001t0014 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 611 | chr5 | 154814707 | ||||||
chr5:154814899 | C | CA | 4 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0023 others(1): Show |
11 | HG01243.hp2 HG01952.hp2 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*819dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 820 | INFO_REALIGN_3_PRIME | chr5 | 154814899 | |||||
chr5:154814899 | CA | C | 1 | a0001c0001t0004 | 10 | HG01255.hp2 HG02257.hp2 HG02258.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*819delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 819 | INFO_REALIGN_3_PRIME | chr5 | 154814899 | |||||
chr5:154815073 | C | T | 1 | a0001c0001t0007 | 5 | HG00735.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*977C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 977 | chr5 | 154815073 | ||||||
chr5:154815645 | G | A | 1 | a0001c0001t0013 | 2 | HG03490.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1549G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 1549 | chr5 | 154815645 | ||||||
chr5:154815868 | C | T | 1 | a0004c0009t0017 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1772C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 1772 | chr5 | 154815868 | ||||||
chr5:154816033 | G | C | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 1937 | chr5 | 154816033 | ||||||
chr5:154816118 | G | A | 2 | a0001c0001t0003 a0001c0001t0018 |
14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2022G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2022 | chr5 | 154816118 | ||||||
chr5:154816132 | C | G | 3 | a0001c0001t0011 a0001c0001t0024 a0001c0010t0011 |
4 | HG01346.hp2 HG01993.hp2 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2036C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2036 | chr5 | 154816132 | ||||||
chr5:154816466 | G | A | 1 | a0001c0001t0009 | 4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2370G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2370 | chr5 | 154816466 | ||||||
chr5:154817017 | C | CT | 3 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0015 |
10 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2936dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2937 | INFO_REALIGN_3_PRIME | chr5 | 154817017 | |||||
chr5:154817032 | TC | T | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(8): Show |
40 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2940delC | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2940 | INFO_REALIGN_3_PRIME | chr5 | 154817032 | |||||
chr5:154817033 | C | T | 13 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(10): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2937C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 2937 | chr5 | 154817033 | ||||||
chr5:154817153 | C | T | 1 | a0001c0001t0016 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3057C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 19/19 | 3057 | chr5 | 154817153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154756242 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.436+49C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756242 | |||||||
chr5:154756344 | C | T | 1 | a0001c0002t0001g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.436+151C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756344 | |||||||
chr5:154756358 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.436+165C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756358 | |||||||
chr5:154756403 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.436+210G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756403 | |||||||
chr5:154756453 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.436+260G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756453 | |||||||
chr5:154756456 | T | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.436+263T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756456 | |||||||
chr5:154756583 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.436+390C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756583 | |||||||
chr5:154756647 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+454C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756647 | |||||||
chr5:154756837 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.436+644C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756837 | |||||||
chr5:154756914 | G | A | 1 | a0001c0001t0009g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.436+721G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756914 | |||||||
chr5:154756933 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.436+740C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756933 | |||||||
chr5:154756949 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.436+756G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756949 | |||||||
chr5:154756960 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+767G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756960 | |||||||
chr5:154756986 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.436+793G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756986 | |||||||
chr5:154756987 | C | G | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.436+794C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154756987 | |||||||
chr5:154757056 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.436+863G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757056 | |||||||
chr5:154757122 | G | A | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
2 | NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.436+929G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757122 | |||||||
chr5:154757132 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.436+939G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757132 | |||||||
chr5:154757231 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0002g0143 |
3 | HG00609.hp2 HG02056.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.436+1038T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757231 | |||||||
chr5:154757283 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.436+1090G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757283 | |||||||
chr5:154757284 | G | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1091G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757284 | |||||||
chr5:154757322 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.436+1129T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757322 | |||||||
chr5:154757331 | G | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0236 a0001c0001t0001g0238 others(13): Show |
18 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.436+1138G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757331 | |||||||
chr5:154757342 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.436+1149C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757342 | |||||||
chr5:154757404 | T | TG | 37 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
39 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.436+1219dupG | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757404 | ||||||
chr5:154757489 | C | G | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0002g0249 |
3 | NA18964.hp2 NA18975.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.436+1296C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757489 | |||||||
chr5:154757500 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.436+1307T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757500 | |||||||
chr5:154757717 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.436+1524G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757717 | |||||||
chr5:154757780 | T | TCCTTCCC others(9): Show |
15 | a0001c0001t0001g0130 a0001c0001t0001g0232 a0001c0001t0001g0233 others(12): Show |
15 | HG00558.hp1 HG01123.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.436+1663_436+1678d others(18): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757780 | ||||||
chr5:154757780 | T | TCCTTCCC others(25): Show |
2 | a0001c0001t0001g0025 a0001c0001t0006g0131 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.436+1647_436+1678d others(34): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757780 | ||||||
chr5:154757780 | TCCTTCCC others(9): Show |
T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(13): Show |
17 | HG00642.hp1 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.436+1663_436+1678d others(18): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757780 | ||||||
chr5:154757780 | TCCTTCCC others(25): Show |
T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
35 | HG00323.hp1 HG01081.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.436+1647_436+1678d others(34): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757780 | ||||||
chr5:154757785 | C | CCCCCCCT others(9): Show |
1 | a0001c0001t0009g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.436+1597_436+1598i others(18): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757785 | ||||||
chr5:154757785 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.436+1592C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757785 | |||||||
chr5:154757801 | CCCCCCTG others(24): Show |
C | 1 | a0001c0001t0002g0277 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.436+1614_436+1644d others(33): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757801 | ||||||
chr5:154757817 | CCCCCCTG others(24): Show |
C | 1 | a0001c0001t0002g0255 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.436+1630_436+1660d others(33): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757817 | ||||||
chr5:154757824 | GCTCCCCT others(41): Show |
G | 1 | a0001c0001t0001g0278 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.436+1645_436+1692d others(50): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757824 | ||||||
chr5:154757832 | TCCCCCCT others(10): Show |
T | 1 | a0001c0001t0001g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436+1645_436+1661d others(19): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757832 | ||||||
chr5:154757833 | CCCCCCTG others(24): Show |
C | 2 | a0001c0001t0001g0279 a0001c0010t0011g0280 |
2 | HG02293.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.436+1646_436+1676d others(33): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757833 | ||||||
chr5:154757849 | CCCCCCTG others(8): Show |
C | 2 | a0001c0001t0001g0030 a0001c0001t0007g0029 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.436+1662_436+1676d others(17): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757849 | ||||||
chr5:154757864 | T | TC | 17 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0087 others(14): Show |
17 | HG00438.hp2 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.436+1677dupC | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757864 | ||||||
chr5:154757868 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.436+1675C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757868 | |||||||
chr5:154757872 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.436+1679C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757872 | |||||||
chr5:154757886 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0002g0148 |
2 | HG03453.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.436+1693T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757886 | |||||||
chr5:154757894 | C | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+1701C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154757894 | |||||||
chr5:154757896 | T | TC | 26 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(23): Show |
26 | HG00438.hp2 HG00597.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.436+1709dupC | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154757896 | ||||||
chr5:154758202 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.436+2009C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758202 | |||||||
chr5:154758223 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+2030C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758223 | |||||||
chr5:154758227 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.436+2034A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758227 | |||||||
chr5:154758329 | G | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0156 others(1): Show |
4 | HG00609.hp2 HG02056.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2136G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758329 | |||||||
chr5:154758503 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.436+2310A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758503 | |||||||
chr5:154758541 | C | A | 7 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(4): Show |
7 | HG00741.hp1 HG01081.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+2348C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758541 | |||||||
chr5:154758845 | A | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(68): Show |
75 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.436+2652A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758845 | |||||||
chr5:154758980 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(68): Show |
75 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.436+2787T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154758980 | |||||||
chr5:154759330 | T | C | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+3137T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154759330 | |||||||
chr5:154759366 | T | C | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.436+3173T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154759366 | |||||||
chr5:154759795 | T | TA | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+3603dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759795 | ||||||
chr5:154759918 | A | AGTTT | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0251 |
3 | HG02165.hp1 HG02630.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.436+3758_436+3761d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759918 | ||||||
chr5:154759918 | AGTTT | A | 59 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(56): Show |
61 | HG00597.hp2 HG01081.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.436+3758_436+3761d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759918 | ||||||
chr5:154759918 | AGTTTGTT others(5): Show |
A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0155 |
2 | HG00544.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.436+3750_436+3761d others(14): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759918 | ||||||
chr5:154759918 | AGTTTGTT others(9): Show |
A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+3746_436+3761d others(18): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759918 | ||||||
chr5:154759939 | GTTTGTTT others(9): Show |
G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436+3751_436+3766d others(18): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759939 | ||||||
chr5:154759947 | GTTTGTTT others(1): Show |
G | 33 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
37 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.436+3759_436+3766d others(10): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759947 | ||||||
chr5:154759951 | GTTTT | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0210 a0001c0001t0013g0064 |
3 | HG03834.hp2 HG04115.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.436+3762_436+3765d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154759951 | ||||||
chr5:154760046 | T | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0140 a0001c0001t0001g0165 others(6): Show |
9 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3853T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760046 | |||||||
chr5:154760064 | A | G | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.436+3871A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760064 | |||||||
chr5:154760091 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.436+3898C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760091 | |||||||
chr5:154760147 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.436+3954A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760147 | |||||||
chr5:154760165 | C | T | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0012g0121 |
3 | HG01243.hp2 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.436+3972C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760165 | |||||||
chr5:154760328 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.436+4135G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760328 | |||||||
chr5:154760440 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.436+4247A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760440 | |||||||
chr5:154760494 | T | C | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+4301T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760494 | |||||||
chr5:154760651 | A | G | 1 | a0001c0001t0002g0249 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.436+4458A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760651 | |||||||
chr5:154760748 | C | G | 1 | a0003c0005t0001g0226 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.436+4555C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760748 | |||||||
chr5:154760882 | A | G | 2 | a0003c0005t0001g0225 a0003c0005t0001g0226 |
2 | HG01934.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.436+4689A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760882 | |||||||
chr5:154760900 | A | G | 16 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(13): Show |
17 | HG01243.hp2 HG01952.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.436+4707A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154760900 | |||||||
chr5:154761215 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.436+5022C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154761215 | |||||||
chr5:154761440 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+5247C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154761440 | |||||||
chr5:154761606 | A | G | 1 | a0001c0001t0020g0224 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.436+5413A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154761606 | |||||||
chr5:154761886 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.436+5693C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154761886 | |||||||
chr5:154761945 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0099 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.436+5752G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154761945 | |||||||
chr5:154762185 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.436+5992G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762185 | |||||||
chr5:154762214 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+6021G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762214 | |||||||
chr5:154762378 | G | A | 1 | a0001c0003t0001g0019 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.436+6185G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762378 | |||||||
chr5:154762497 | G | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(82): Show |
89 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.436+6304G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762497 | |||||||
chr5:154762531 | C | CT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+6346dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154762531 | ||||||
chr5:154762677 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
15 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.436+6484G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762677 | |||||||
chr5:154762980 | C | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(70): Show |
77 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.436+6787C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154762980 | |||||||
chr5:154763025 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18950.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.436+6832T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763025 | |||||||
chr5:154763054 | C | CT | 29 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0022 others(26): Show |
29 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.436+6879dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154763054 | ||||||
chr5:154763054 | CT | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(27): Show |
32 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.436+6879delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154763054 | ||||||
chr5:154763054 | CTT | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
39 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.436+6878_436+6879d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154763054 | ||||||
chr5:154763097 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+6904C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763097 | |||||||
chr5:154763098 | G | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+6905G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763098 | |||||||
chr5:154763102 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.436+6909C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763102 | |||||||
chr5:154763137 | C | T | 11 | a0001c0002t0001g0013 a0001c0002t0001g0152 a0001c0002t0001g0215 others(8): Show |
12 | HG00639.hp2 HG01071.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.436+6944C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763137 | |||||||
chr5:154763152 | C | T | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+6959C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763152 | |||||||
chr5:154763293 | C | A | 1 | a0001c0001t0013g0064 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.436+7100C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763293 | |||||||
chr5:154763298 | G | A | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.436+7105G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763298 | |||||||
chr5:154763384 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.436+7191C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763384 | |||||||
chr5:154763519 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0147 a0001c0001t0001g0163 others(2): Show |
6 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+7326C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763519 | |||||||
chr5:154763576 | C | G | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436+7383C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763576 | |||||||
chr5:154763645 | T | G | 1 | a0001c0001t0022g0171 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.436+7452T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763645 | |||||||
chr5:154763747 | AC | A | 6 | a0001c0001t0001g0068 a0001c0001t0004g0067 a0001c0001t0008g0031 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+7558delC | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154763747 | ||||||
chr5:154763843 | C | CA | 24 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(21): Show |
25 | HG01243.hp2 HG01952.hp2 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.436+7662dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154763843 | ||||||
chr5:154763850 | A | C | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+7657A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763850 | |||||||
chr5:154763934 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+7741A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763934 | |||||||
chr5:154763938 | T | G | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.436+7745T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154763938 | |||||||
chr5:154764142 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.436+7949C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764142 | |||||||
chr5:154764170 | G | A | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0012g0121 |
3 | HG01243.hp2 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.436+7977G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764170 | |||||||
chr5:154764195 | A | C | 64 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(61): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.436+8002A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764195 | |||||||
chr5:154764309 | C | CA | 16 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(13): Show |
17 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.436+8131dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764309 | ||||||
chr5:154764372 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.436+8179T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764372 | |||||||
chr5:154764533 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0147 a0001c0001t0001g0213 |
4 | HG02572.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+8340C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764533 | |||||||
chr5:154764548 | C | CT | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.436+8355_436+8356i others(3): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764548 | |||||||
chr5:154764550 | A | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.436+8357A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764550 | |||||||
chr5:154764595 | C | CA | 84 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0023 others(81): Show |
87 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.436+8427dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764595 | ||||||
chr5:154764595 | C | CAA | 57 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0030 others(54): Show |
59 | HG00639.hp1 HG00738.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.436+8426_436+8427d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764595 | ||||||
chr5:154764595 | C | CAAA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG00558.hp1 HG00597.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.436+8425_436+8427d others(5): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764595 | ||||||
chr5:154764624 | G | T | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.436+8431G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764624 | |||||||
chr5:154764632 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(36): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.436+8439T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764632 | |||||||
chr5:154764643 | A | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(10): Show |
14 | HG01952.hp2 HG01978.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+8450A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764643 | |||||||
chr5:154764899 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+8706C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764899 | |||||||
chr5:154764904 | C | CA | 13 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0140 others(10): Show |
13 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.436+8726dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764904 | ||||||
chr5:154764904 | CA | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(67): Show |
74 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(71): Show |
intron_variant | MODIFIER | c.436+8726delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154764904 | ||||||
chr5:154764968 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.436+8775C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154764968 | |||||||
chr5:154765090 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.436+8897T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765090 | |||||||
chr5:154765104 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.436+8911G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765104 | |||||||
chr5:154765119 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0016g0122 |
2 | HG02886.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.436+8926G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765119 | |||||||
chr5:154765247 | C | G | 2 | a0001c0001t0006g0125 a0001c0001t0015g0124 |
2 | HG02895.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.436+9054C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765247 | |||||||
chr5:154765401 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.436+9208G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765401 | |||||||
chr5:154765405 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.436+9212C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765405 | |||||||
chr5:154765446 | A | G | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.436+9253A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765446 | |||||||
chr5:154765500 | T | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(68): Show |
75 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(72): Show |
intron_variant | MODIFIER | c.436+9307T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765500 | |||||||
chr5:154765566 | T | A | 35 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(32): Show |
37 | HG00558.hp1 HG01243.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.436+9373T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765566 | |||||||
chr5:154765594 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.436+9401A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765594 | |||||||
chr5:154765914 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.436+9721G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154765914 | |||||||
chr5:154766034 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.436+9841G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766034 | |||||||
chr5:154766071 | G | A | 13 | a0001c0001t0003g0006 a0001c0001t0003g0045 a0001c0001t0003g0074 others(10): Show |
14 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+9878G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766071 | |||||||
chr5:154766126 | A | G | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+9933A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766126 | |||||||
chr5:154766474 | A | G | 4 | a0001c0001t0008g0031 a0001c0001t0008g0032 a0001c0001t0008g0044 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+10281A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766474 | |||||||
chr5:154766478 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+10285G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766478 | |||||||
chr5:154766660 | T | G | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436+10467T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766660 | |||||||
chr5:154766674 | C | T | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436+10481C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154766674 | |||||||
chr5:154767127 | CAGTT | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0033 a0001c0001t0007g0069 others(1): Show |
4 | HG02451.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+10937_436+1094 others(8): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154767127 | ||||||
chr5:154767271 | T | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+11078T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767271 | |||||||
chr5:154767346 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.436+11153C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767346 | |||||||
chr5:154767636 | C | A | 1 | a0001c0001t0014g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.436+11443C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767636 | |||||||
chr5:154767671 | G | A | 3 | a0002c0004t0001g0015 a0002c0004t0001g0259 a0002c0004t0002g0015 |
3 | HG02280.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.436+11478G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767671 | |||||||
chr5:154767846 | G | A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+11653G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767846 | |||||||
chr5:154767915 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436+11722A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154767915 | |||||||
chr5:154768216 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.436+12023C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768216 | |||||||
chr5:154768556 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+12363C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768556 | |||||||
chr5:154768562 | T | A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0002g0249 |
3 | NA18964.hp2 NA18975.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.436+12369T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768562 | |||||||
chr5:154768570 | A | ATT | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+12379_436+1238 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154768570 | ||||||
chr5:154768576 | T | TTA | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+12384_436+1238 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154768576 | ||||||
chr5:154768729 | G | A | 1 | a0001c0001t0006g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.436+12536G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768729 | |||||||
chr5:154768817 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+12624G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768817 | |||||||
chr5:154768820 | A | G | 5 | a0001c0001t0007g0029 a0001c0001t0007g0033 a0001c0001t0007g0069 others(2): Show |
5 | HG00735.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+12627A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768820 | |||||||
chr5:154768848 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.436+12655T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154768848 | |||||||
chr5:154769145 | T | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
15 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.436+12952T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769145 | |||||||
chr5:154769171 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG00741.hp1 HG01081.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+12978G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769171 | |||||||
chr5:154769244 | A | C | 13 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0173 others(10): Show |
13 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.436+13051A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769244 | |||||||
chr5:154769302 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(36): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.436+13109T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769302 | |||||||
chr5:154769310 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+13117G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769310 | |||||||
chr5:154769369 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.436+13176G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769369 | |||||||
chr5:154769505 | G | A | 2 | a0003c0005t0001g0225 a0003c0005t0001g0226 |
2 | HG01934.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.436+13312G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769505 | |||||||
chr5:154769535 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0212 |
2 | HG00438.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.436+13342A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769535 | |||||||
chr5:154769642 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0058 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.436+13449T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154769642 | |||||||
chr5:154770086 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+13893G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770086 | |||||||
chr5:154770232 | AT | A | 10 | a0001c0001t0001g0109 a0001c0001t0001g0166 a0001c0001t0001g0260 others(7): Show |
10 | HG00558.hp1 HG01257.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.436+14055delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154770232 | ||||||
chr5:154770278 | A | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.436+14085A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770278 | |||||||
chr5:154770370 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+14177C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770370 | |||||||
chr5:154770407 | T | C | 4 | a0001c0001t0011g0256 a0001c0001t0011g0266 a0001c0001t0024g0265 others(1): Show |
4 | HG01346.hp2 HG01993.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+14214T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770407 | |||||||
chr5:154770471 | G | A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+14278G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770471 | |||||||
chr5:154770492 | C | T | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0102 others(5): Show |
8 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+14299C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770492 | |||||||
chr5:154770559 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+14366A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770559 | |||||||
chr5:154770713 | G | A | 1 | a0002c0004t0001g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.436+14520G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770713 | |||||||
chr5:154770749 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.436+14556G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770749 | |||||||
chr5:154770828 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.436+14635C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770828 | |||||||
chr5:154770840 | C | T | 5 | a0001c0001t0001g0178 a0001c0001t0001g0188 a0001c0001t0001g0189 others(2): Show |
5 | HG01106.hp1 HG01123.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+14647C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770840 | |||||||
chr5:154770891 | T | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(61): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.436+14698T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154770891 | |||||||
chr5:154771015 | G | A | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.436+14822G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154771015 | |||||||
chr5:154771067 | G | A | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
15 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.436+14874G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154771067 | |||||||
chr5:154771092 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(70): Show |
77 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.436+14899G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154771092 | |||||||
chr5:154771116 | G | GA | 65 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(62): Show |
68 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.436+14938dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154771116 | ||||||
chr5:154771116 | G | GAA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(3): Show |
7 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+14937_436+1493 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154771116 | ||||||
chr5:154771503 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436+15310T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154771503 | |||||||
chr5:154771745 | T | C | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.436+15552T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154771745 | |||||||
chr5:154772206 | ATAATC | A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+16018_436+1602 others(9): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154772206 | ||||||
chr5:154772235 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.436+16042A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154772235 | |||||||
chr5:154772264 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.436+16071T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154772264 | |||||||
chr5:154772494 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.436+16301C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154772494 | |||||||
chr5:154772880 | T | A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.436+16687T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154772880 | |||||||
chr5:154772942 | A | G | 1 | a0001c0008t0001g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.436+16749A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154772942 | |||||||
chr5:154772980 | C | CT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(51): Show |
59 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.436+16810dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154772980 | ||||||
chr5:154772980 | C | CTT | 7 | a0001c0001t0001g0109 a0001c0001t0002g0255 a0001c0001t0011g0256 others(4): Show |
7 | HG01346.hp2 HG01993.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+16809_436+1681 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154772980 | ||||||
chr5:154772980 | CT | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0048 a0001c0001t0001g0058 others(8): Show |
11 | HG01069.hp2 HG01099.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.436+16810delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154772980 | ||||||
chr5:154773108 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+16915C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773108 | |||||||
chr5:154773362 | G | C | 1 | a0001c0001t0003g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.437-16963G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773362 | |||||||
chr5:154773415 | A | G | 3 | a0002c0004t0001g0015 a0002c0004t0001g0259 a0002c0004t0002g0015 |
3 | HG02280.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.437-16910A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773415 | |||||||
chr5:154773586 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.437-16739C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773586 | |||||||
chr5:154773790 | C | T | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-16535C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773790 | |||||||
chr5:154773865 | G | C | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437-16460G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773865 | |||||||
chr5:154773888 | G | C | 1 | a0001c0002t0001g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.437-16437G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773888 | |||||||
chr5:154773952 | C | T | 1 | a0001c0001t0001g0017 | 2 | NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.437-16373C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154773952 | |||||||
chr5:154774037 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(69): Show |
76 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.437-16288A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774037 | |||||||
chr5:154774049 | A | AT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(54): Show |
60 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(57): Show |
intron_variant | MODIFIER | c.437-16261dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154774049 | ||||||
chr5:154774152 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.437-16173T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774152 | |||||||
chr5:154774185 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.437-16140G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774185 | |||||||
chr5:154774358 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-15967C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774358 | |||||||
chr5:154774391 | G | C | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-15934G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774391 | |||||||
chr5:154774458 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(70): Show |
77 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.437-15867A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774458 | |||||||
chr5:154774491 | G | A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-15834G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154774491 | |||||||
chr5:154775001 | C | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-15324C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775001 | |||||||
chr5:154775294 | C | T | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0012g0121 |
3 | HG01243.hp2 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.437-15031C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775294 | |||||||
chr5:154775387 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.437-14938G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775387 | |||||||
chr5:154775390 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437-14935G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775390 | |||||||
chr5:154775493 | C | CA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
19 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-14816dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154775493 | ||||||
chr5:154775493 | CA | C | 17 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0231 others(14): Show |
18 | HG00735.hp1 HG01952.hp2 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.437-14816delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154775493 | ||||||
chr5:154775674 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.437-14651A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775674 | |||||||
chr5:154775682 | C | T | 2 | a0001c0001t0006g0129 a0001c0001t0012g0127 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.437-14643C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154775682 | |||||||
chr5:154776221 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.437-14104G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776221 | |||||||
chr5:154776269 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-14056T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776269 | |||||||
chr5:154776316 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-14009G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776316 | |||||||
chr5:154776349 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.437-13976C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776349 | |||||||
chr5:154776376 | A | T | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-13949A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776376 | |||||||
chr5:154776694 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.437-13631G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776694 | |||||||
chr5:154776913 | T | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.437-13412T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776913 | |||||||
chr5:154776984 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-13341G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154776984 | |||||||
chr5:154777069 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.437-13256A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777069 | |||||||
chr5:154777223 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-13102G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777223 | |||||||
chr5:154777290 | C | T | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-13035C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777290 | |||||||
chr5:154777315 | A | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0140 others(9): Show |
12 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-13010A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777315 | |||||||
chr5:154777348 | T | TA | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.437-12962dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154777348 | ||||||
chr5:154777616 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437-12709T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777616 | |||||||
chr5:154777692 | T | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0279 |
2 | HG02080.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.437-12633T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777692 | |||||||
chr5:154777774 | C | T | 4 | a0001c0002t0001g0013 a0001c0002t0001g0152 a0001c0002t0001g0218 others(1): Show |
5 | HG01515.hp2 HG01517.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-12551C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777774 | |||||||
chr5:154777849 | T | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG00140.hp2 HG00642.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-12476T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777849 | |||||||
chr5:154777852 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-12473A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777852 | |||||||
chr5:154777954 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.437-12371T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154777954 | |||||||
chr5:154778144 | C | T | 8 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0050 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-12181C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778144 | |||||||
chr5:154778175 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0004g0067 a0001c0001t0007g0029 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-12150G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778175 | |||||||
chr5:154778177 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.437-12148G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778177 | |||||||
chr5:154778258 | T | TA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
9 | HG00642.hp1 HG01175.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.437-12048dupA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154778258 | ||||||
chr5:154778258 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-12057_437-1204 others(14): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154778258 | ||||||
chr5:154778258 | T | TTAAAAAA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(20): Show |
25 | HG01081.hp1 HG01123.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.437-12067_437-1206 others(11): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778258 | |||||||
chr5:154778258 | T | TTAAAAAA others(1): Show |
6 | a0001c0001t0001g0262 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01255.hp1 HG01975.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-12067_437-1206 others(12): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778258 | |||||||
chr5:154778258 | T | TTAAAAAA others(2): Show |
3 | a0001c0001t0001g0264 a0001c0001t0001g0269 a0001c0001t0002g0277 |
3 | HG00597.hp2 HG02148.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.437-12067_437-1206 others(13): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778258 | |||||||
chr5:154778258 | T | TTAAAAAA others(3): Show |
1 | a0001c0001t0005g0258 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.437-12067_437-1206 others(14): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778258 | |||||||
chr5:154778258 | TA | T | 30 | a0001c0001t0001g0109 a0001c0001t0001g0115 a0001c0001t0001g0117 others(27): Show |
31 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(28): Show |
intron_variant | MODIFIER | c.437-12048delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154778258 | ||||||
chr5:154778381 | G | C | 1 | a0001c0001t0004g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.437-11944G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778381 | |||||||
chr5:154778531 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.437-11794T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778531 | |||||||
chr5:154778622 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.437-11703A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778622 | |||||||
chr5:154778732 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.437-11593C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154778732 | |||||||
chr5:154779036 | C | CT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(36): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.437-11282dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154779036 | ||||||
chr5:154779505 | C | CT | 51 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0016 others(48): Show |
53 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.437-10800dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154779505 | ||||||
chr5:154779505 | CT | C | 31 | a0001c0001t0001g0058 a0001c0001t0001g0088 a0001c0001t0001g0103 others(28): Show |
32 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.437-10800delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154779505 | ||||||
chr5:154779507 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.437-10818T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779507 | |||||||
chr5:154779569 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.437-10756C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779569 | |||||||
chr5:154779578 | G | A | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-10747G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779578 | |||||||
chr5:154779698 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0087 a0001c0001t0001g0089 others(2): Show |
5 | HG00140.hp1 HG00738.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-10627G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779698 | |||||||
chr5:154779827 | G | T | 26 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0130 others(23): Show |
27 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.437-10498G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779827 | |||||||
chr5:154779947 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.437-10378T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779947 | |||||||
chr5:154779970 | T | C | 1 | a0001c0001t0006g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.437-10355T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154779970 | |||||||
chr5:154780029 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-10296C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780029 | |||||||
chr5:154780117 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.437-10208G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780117 | |||||||
chr5:154780219 | T | C | 11 | a0001c0001t0001g0068 a0001c0001t0004g0067 a0001c0001t0007g0029 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-10106T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780219 | |||||||
chr5:154780577 | C | A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-9748C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780577 | |||||||
chr5:154780773 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0140 others(9): Show |
12 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-9552G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780773 | |||||||
chr5:154780891 | A | G | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(70): Show |
77 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(74): Show |
intron_variant | MODIFIER | c.437-9434A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780891 | |||||||
chr5:154780982 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.437-9343G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154780982 | |||||||
chr5:154781047 | T | C | 160 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(157): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.437-9278T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781047 | |||||||
chr5:154781064 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.437-9261G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781064 | |||||||
chr5:154781076 | A | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0096 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-9249A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781076 | |||||||
chr5:154781182 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437-9143C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781182 | |||||||
chr5:154781336 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0007g0033 a0001c0001t0007g0069 others(2): Show |
5 | HG00735.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-8989G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781336 | |||||||
chr5:154781368 | C | T | 9 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0125 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.437-8957C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781368 | |||||||
chr5:154781375 | C | T | 8 | a0001c0001t0001g0262 a0001c0001t0001g0264 a0001c0001t0001g0269 others(5): Show |
8 | HG00597.hp2 HG01255.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-8950C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781375 | |||||||
chr5:154781418 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.437-8907C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781418 | |||||||
chr5:154781420 | G | T | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-8905G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781420 | |||||||
chr5:154781434 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.437-8891T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781434 | |||||||
chr5:154781473 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.437-8852A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781473 | |||||||
chr5:154781517 | T | C | 14 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
14 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.437-8808T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781517 | |||||||
chr5:154781550 | G | A | 2 | a0001c0001t0006g0129 a0001c0001t0012g0127 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.437-8775G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781550 | |||||||
chr5:154781551 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.437-8774C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781551 | |||||||
chr5:154781589 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-8736G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781589 | |||||||
chr5:154781613 | A | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-8712A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781613 | |||||||
chr5:154781694 | G | A | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-8631G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781694 | |||||||
chr5:154781695 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.437-8630G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781695 | |||||||
chr5:154781705 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.437-8620C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781705 | |||||||
chr5:154781803 | C | T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.437-8522C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781803 | |||||||
chr5:154781905 | T | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-8420T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154781905 | |||||||
chr5:154782216 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.437-8109G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782216 | |||||||
chr5:154782480 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.437-7845C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782480 | |||||||
chr5:154782570 | C | T | 1 | a0001c0003t0001g0118 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.437-7755C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782570 | |||||||
chr5:154782585 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.437-7740C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782585 | |||||||
chr5:154782766 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.437-7559T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782766 | |||||||
chr5:154782808 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.437-7517C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154782808 | |||||||
chr5:154783005 | A | T | 1 | a0001c0002t0001g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.437-7320A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783005 | |||||||
chr5:154783042 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.437-7283G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783042 | |||||||
chr5:154783191 | A | T | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
52 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.437-7134A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783191 | |||||||
chr5:154783202 | C | CT | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-7122dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154783202 | ||||||
chr5:154783289 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.437-7036A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783289 | |||||||
chr5:154783356 | G | A | 13 | a0001c0002t0001g0013 a0001c0002t0001g0152 a0001c0002t0001g0200 others(10): Show |
14 | HG00639.hp2 HG01071.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.437-6969G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783356 | |||||||
chr5:154783418 | C | T | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.437-6907C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783418 | |||||||
chr5:154783496 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.437-6829G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783496 | |||||||
chr5:154783518 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.437-6807T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783518 | |||||||
chr5:154783726 | C | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(234): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.437-6599C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154783726 | |||||||
chr5:154784032 | G | T | 2 | a0001c0001t0006g0110 a0001c0001t0006g0111 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.437-6293G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154784032 | |||||||
chr5:154784033 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.437-6292C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154784033 | |||||||
chr5:154784525 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.437-5800G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154784525 | |||||||
chr5:154784888 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.437-5437A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154784888 | |||||||
chr5:154785006 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
2 | NA18942.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.437-5319A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785006 | |||||||
chr5:154785144 | C | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
37 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.437-5181C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785144 | |||||||
chr5:154785177 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.437-5148C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785177 | |||||||
chr5:154785179 | A | G | 1 | a0001c0002t0001g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.437-5146A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785179 | |||||||
chr5:154785307 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.437-5018C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785307 | |||||||
chr5:154785415 | G | A | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.437-4910G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785415 | |||||||
chr5:154785420 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0212 |
2 | HG00438.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.437-4905C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785420 | |||||||
chr5:154785423 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.437-4902G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785423 | |||||||
chr5:154785702 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-4623T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785702 | |||||||
chr5:154785741 | G | A | 1 | a0001c0008t0001g0230 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.437-4584G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785741 | |||||||
chr5:154785746 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0006g0126 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.437-4579C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785746 | |||||||
chr5:154785786 | A | G | 1 | a0001c0001t0022g0171 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.437-4539A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154785786 | |||||||
chr5:154786028 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.437-4297T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786028 | |||||||
chr5:154786038 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-4287G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786038 | |||||||
chr5:154786039 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.437-4286G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786039 | |||||||
chr5:154786104 | G | A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-4221G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786104 | |||||||
chr5:154786129 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0102 others(5): Show |
8 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-4196G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786129 | |||||||
chr5:154786222 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.437-4103G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786222 | |||||||
chr5:154786261 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-4064T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786261 | |||||||
chr5:154786345 | T | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02109.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.437-3980T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786345 | |||||||
chr5:154786410 | A | G | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-3915A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786410 | |||||||
chr5:154786445 | T | A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.437-3880T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786445 | |||||||
chr5:154786453 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0140 others(9): Show |
12 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.437-3872A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786453 | |||||||
chr5:154786480 | C | T | 8 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0050 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-3845C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786480 | |||||||
chr5:154786524 | A | AG | 3 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0196 |
3 | HG00438.hp1 HG01993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.437-3798dupG | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154786524 | ||||||
chr5:154786571 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-3754C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786571 | |||||||
chr5:154786816 | C | A | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437-3509C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786816 | |||||||
chr5:154786882 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.437-3443T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786882 | |||||||
chr5:154786894 | T | G | 4 | a0001c0001t0011g0256 a0002c0004t0001g0015 a0002c0004t0001g0259 others(1): Show |
4 | HG02280.hp2 HG02300.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-3431T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786894 | |||||||
chr5:154786895 | T | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(37): Show |
43 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(40): Show |
intron_variant | MODIFIER | c.437-3430T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786895 | |||||||
chr5:154786960 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.437-3365C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154786960 | |||||||
chr5:154787320 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.437-3005A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154787320 | |||||||
chr5:154787644 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.437-2681C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154787644 | |||||||
chr5:154787658 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.437-2667G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154787658 | |||||||
chr5:154788092 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.437-2233G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788092 | |||||||
chr5:154788178 | G | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0144 a0001c0001t0001g0156 others(1): Show |
4 | HG00609.hp2 HG02056.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-2147G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788178 | |||||||
chr5:154788233 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.437-2092G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788233 | |||||||
chr5:154788288 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.437-2037G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788288 | |||||||
chr5:154788390 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.437-1935G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788390 | |||||||
chr5:154788605 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.437-1720G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788605 | |||||||
chr5:154788632 | T | C | 41 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
43 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.437-1693T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788632 | |||||||
chr5:154788647 | G | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.437-1678G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788647 | |||||||
chr5:154788659 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.437-1666G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788659 | |||||||
chr5:154788688 | G | A | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.437-1637G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154788688 | |||||||
chr5:154788743 | TA | T | 10 | a0001c0001t0001g0117 a0001c0001t0004g0106 a0001c0001t0006g0125 others(7): Show |
10 | HG01168.hp2 HG01346.hp2 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1568delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154788743 | ||||||
chr5:154789069 | G | A | 1 | a0001c0006t0001g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.437-1256G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789069 | |||||||
chr5:154789083 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0005g0057 |
3 | HG02717.hp1 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.437-1242C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789083 | |||||||
chr5:154789136 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.437-1189G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789136 | |||||||
chr5:154789219 | C | CT | 58 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(55): Show |
60 | HG00558.hp1 HG00735.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.437-1086dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154789219 | ||||||
chr5:154789219 | C | CTT | 80 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0016 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.437-1087_437-1086d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154789219 | ||||||
chr5:154789219 | C | CTTT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
10 | HG01952.hp1 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.437-1088_437-1086d others(5): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 154789219 | ||||||
chr5:154789258 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0268 |
3 | NA18951.hp1 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.437-1067C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789258 | |||||||
chr5:154789455 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.437-870G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789455 | |||||||
chr5:154789466 | C | T | 8 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0102 others(5): Show |
8 | HG01099.hp1 HG01168.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.437-859C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789466 | |||||||
chr5:154789889 | G | T | 4 | a0001c0001t0006g0126 a0001c0001t0006g0128 a0001c0001t0006g0129 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-436G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154789889 | |||||||
chr5:154790030 | C | T | 16 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(13): Show |
17 | HG01243.hp2 HG01952.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.437-295C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154790030 | |||||||
chr5:154790179 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.437-146G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154790179 | |||||||
chr5:154790181 | G | A | 11 | a0001c0001t0001g0068 a0001c0001t0004g0067 a0001c0001t0007g0029 others(8): Show |
11 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-144G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154790181 | |||||||
chr5:154790284 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.437-41A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 1/18 | chr5 | 154790284 | |||||||
chr5:154790789 | C | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.564+79C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154790789 | |||||||
chr5:154791134 | G | GT | 28 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0078 others(25): Show |
28 | HG00621.hp2 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.564+442dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 154791134 | ||||||
chr5:154791134 | GT | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(34): Show |
40 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.564+442delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 154791134 | ||||||
chr5:154791138 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.564+428T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791138 | |||||||
chr5:154791239 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.564+529A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791239 | |||||||
chr5:154791274 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564+564T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791274 | |||||||
chr5:154791483 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.564+773A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791483 | |||||||
chr5:154791534 | G | A | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+824G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791534 | |||||||
chr5:154791554 | A | C | 1 | a0001c0001t0001g0150 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.564+844A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791554 | |||||||
chr5:154791633 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.564+923T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791633 | |||||||
chr5:154791640 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.564+930C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791640 | |||||||
chr5:154791706 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0009g0136 a0001c0001t0009g0137 others(2): Show |
5 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.565-916C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791706 | |||||||
chr5:154791770 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.565-852A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791770 | |||||||
chr5:154791970 | G | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(36): Show |
42 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.565-652G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154791970 | |||||||
chr5:154792011 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.565-611C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154792011 | |||||||
chr5:154792040 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.565-582G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154792040 | |||||||
chr5:154792126 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.565-496G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154792126 | |||||||
chr5:154792252 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.565-370T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 3/18 | chr5 | 154792252 | |||||||
chr5:154792937 | A | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(2): Show |
5 | HG00323.hp2 HG01106.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.739+141A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154792937 | |||||||
chr5:154793228 | G | T | 1 | a0001c0001t0002g0277 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.740-367G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154793228 | |||||||
chr5:154793349 | G | T | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.740-246G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154793349 | |||||||
chr5:154793362 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.740-233C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154793362 | |||||||
chr5:154793412 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0087 a0001c0001t0001g0090 others(1): Show |
4 | HG00140.hp1 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-183C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154793412 | |||||||
chr5:154793508 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.740-87C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 4/18 | chr5 | 154793508 | |||||||
chr5:154794434 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1232+172T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154794434 | |||||||
chr5:154794464 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1232+202A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154794464 | |||||||
chr5:154794587 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02109.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1232+325G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154794587 | |||||||
chr5:154794697 | C | T | 1 | a0001c0001t0007g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1232+435C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154794697 | |||||||
chr5:154794979 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1233-196A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154794979 | |||||||
chr5:154795034 | A | G | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1233-141A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154795034 | |||||||
chr5:154795167 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18747.hp2 | splice_region_variant&intron_variant | LOW | c.1233-8C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 7/18 | chr5 | 154795167 | |||||||
chr5:154795416 | T | C | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1377+97T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795416 | |||||||
chr5:154795620 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1377+301C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795620 | |||||||
chr5:154795716 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0109 |
3 | HG02486.hp1 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1377+397C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795716 | |||||||
chr5:154795809 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(10): Show |
14 | HG01952.hp2 HG01978.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1377+490C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795809 | |||||||
chr5:154795811 | CCATA | C | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1377+493_1377+496d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795811 | |||||||
chr5:154795823 | TTA | T | 25 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(22): Show |
28 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.1377+514_1377+515d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795823 | ||||||
chr5:154795825 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0201 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1377+513_1377+514i others(21): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795825 | ||||||
chr5:154795838 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0046 a0001c0001t0001g0096 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1377+519A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795838 | |||||||
chr5:154795916 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1377+597A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154795916 | |||||||
chr5:154795918 | ATATT | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1377+603_1377+606d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795918 | ||||||
chr5:154795928 | TTATA | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02109.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1377+613_1377+616d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795928 | ||||||
chr5:154795950 | TTA | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(35): Show |
41 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1377+639_1377+640d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795950 | ||||||
chr5:154795986 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0239 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1377+709_1377+744d others(38): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795986 | ||||||
chr5:154795986 | TTATATAT others(29): Show |
T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1377+709_1377+744d others(38): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795986 | ||||||
chr5:154795998 | ATATATAT others(8): Show |
A | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1377+694_1377+708d others(17): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154795998 | ||||||
chr5:154796017 | ATATTATA others(5): Show |
A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1377+700_1377+711d others(14): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796017 | ||||||
chr5:154796023 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1377+704T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796023 | |||||||
chr5:154796034 | A | ATATATAT others(23): Show |
1 | a0001c0001t0009g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1377+723_1377+752d others(32): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796034 | ||||||
chr5:154796055 | A | ATTATATA others(32): Show |
1 | a0001c0001t0001g0180 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1377+773_1377+811d others(41): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796055 | ||||||
chr5:154796082 | TTA | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0109 a0001c0001t0001g0115 |
3 | HG01928.hp2 HG01978.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1377+773_1377+774d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796082 | ||||||
chr5:154796084 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0010 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1377+766_1377+787d others(24): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796084 | ||||||
chr5:154796094 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1377+775T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796094 | |||||||
chr5:154796114 | A | ATATATAT others(19): Show |
1 | a0001c0003t0001g0118 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1377+812_1377+837d others(28): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796114 | ||||||
chr5:154796121 | T | TTATATAT others(21): Show |
28 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0115 others(25): Show |
30 | HG00558.hp1 HG01243.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1377+817_1377+844d others(30): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796121 | ||||||
chr5:154796121 | T | TTATATAT others(49): Show |
4 | a0001c0001t0001g0024 a0001c0001t0009g0136 a0001c0001t0009g0137 others(1): Show |
4 | HG02080.hp2 HG02129.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377+844_1377+845i others(58): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796121 | ||||||
chr5:154796121 | T | TTATATAT others(77): Show |
1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1377+844_1377+845i others(86): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796121 | ||||||
chr5:154796136 | ATATTTAT others(21): Show |
A | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1377+845_1377+872d others(30): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154796136 | ||||||
chr5:154796146 | A | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0279 |
2 | HG02080.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1377+827A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796146 | |||||||
chr5:154796147 | T | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0279 |
2 | HG02080.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1377+828T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796147 | |||||||
chr5:154796164 | G | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(42): Show |
48 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1377+845G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796164 | |||||||
chr5:154796297 | A | G | 1 | a0001c0001t0001g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1377+978A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796297 | |||||||
chr5:154796572 | C | A | 1 | a0001c0001t0001g0253 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1377+1253C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796572 | |||||||
chr5:154796617 | A | G | 2 | a0001c0001t0007g0029 a0001c0001t0007g0033 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1377+1298A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796617 | |||||||
chr5:154796874 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1377+1555A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154796874 | |||||||
chr5:154797214 | T | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0140 others(9): Show |
12 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1377+1895T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797214 | |||||||
chr5:154797218 | GTTGTTTT others(1): Show |
G | 7 | a0001c0001t0001g0260 a0001c0001t0001g0264 a0001c0001t0001g0272 others(4): Show |
7 | HG01346.hp2 HG01993.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377+1902_1377+190 others(12): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797218 | ||||||
chr5:154797218 | GTTGTTTT others(2): Show |
G | 25 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(22): Show |
27 | HG00597.hp2 HG01123.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.1377+1902_1377+191 others(13): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797218 | ||||||
chr5:154797218 | GTTGTTTT others(3): Show |
G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0279 |
2 | HG01081.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1377+1902_1377+191 others(14): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797218 | ||||||
chr5:154797221 | G | GT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0056 a0001c0001t0001g0058 others(27): Show |
30 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1377+1931dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797221 | ||||||
chr5:154797221 | GT | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(83): Show |
88 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1377+1931delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797221 | ||||||
chr5:154797221 | GTT | G | 12 | a0001c0001t0001g0025 a0001c0001t0001g0166 a0001c0001t0001g0245 others(9): Show |
12 | HG01109.hp1 HG01257.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.1377+1930_1377+193 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797221 | ||||||
chr5:154797221 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1377+1921_1377+193 others(15): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797221 | ||||||
chr5:154797221 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1377+1917_1377+193 others(19): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797221 | ||||||
chr5:154797224 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1377+1905T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797224 | |||||||
chr5:154797229 | T | G | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1377+1910T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797229 | |||||||
chr5:154797234 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1377+1915T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797234 | |||||||
chr5:154797306 | T | C | 1 | a0001c0001t0004g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1377+1987T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797306 | |||||||
chr5:154797316 | C | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0147 a0001c0001t0001g0163 others(5): Show |
9 | HG01884.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1377+1997C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797316 | |||||||
chr5:154797680 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0268 others(13): Show |
17 | HG01243.hp1 HG02080.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378-1895dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797680 | ||||||
chr5:154797680 | C | CTT | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(35): Show |
41 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1378-1896_1378-189 others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797680 | ||||||
chr5:154797680 | CT | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0036 others(9): Show |
12 | HG01517.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1378-1895delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154797680 | ||||||
chr5:154797854 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1378-1737T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797854 | |||||||
chr5:154797866 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378-1725G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797866 | |||||||
chr5:154797949 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0196 |
2 | HG01993.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1378-1642G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154797949 | |||||||
chr5:154798131 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1378-1460G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798131 | |||||||
chr5:154798140 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1378-1451C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798140 | |||||||
chr5:154798188 | C | T | 13 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(10): Show |
14 | HG01952.hp2 HG01978.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378-1403C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798188 | |||||||
chr5:154798189 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1378-1402G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798189 | |||||||
chr5:154798401 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0058 |
2 | HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1378-1190G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798401 | |||||||
chr5:154798544 | C | G | 3 | a0002c0004t0001g0015 a0002c0004t0001g0259 a0002c0004t0002g0015 |
3 | HG02280.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1378-1047C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798544 | |||||||
chr5:154798622 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1378-969C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798622 | |||||||
chr5:154798647 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1378-944G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798647 | |||||||
chr5:154798855 | T | TTTTG | 26 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0115 others(23): Show |
28 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(25): Show |
intron_variant | MODIFIER | c.1378-711_1378-708d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154798855 | ||||||
chr5:154798855 | TTTTG | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378-711_1378-708d others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154798855 | ||||||
chr5:154798887 | C | T | 1 | a0001c0003t0001g0042 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1378-704C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798887 | |||||||
chr5:154798968 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0241 a0001c0001t0002g0002 others(1): Show |
6 | HG00609.hp1 HG02129.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1378-623G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154798968 | |||||||
chr5:154799014 | C | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0173 others(11): Show |
14 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1378-577C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154799014 | |||||||
chr5:154799125 | G | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.1378-466G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154799125 | |||||||
chr5:154799197 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1378-394A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154799197 | |||||||
chr5:154799316 | C | CCCTGTTT others(28): Show |
1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1378-243_1378-242i others(37): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr5 | 154799316 | ||||||
chr5:154799473 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1378-118T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 8/18 | chr5 | 154799473 | |||||||
chr5:154799780 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+21A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 9/18 | chr5 | 154799780 | |||||||
chr5:154799797 | T | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546+38T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 9/18 | chr5 | 154799797 | |||||||
chr5:154800069 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1716+27G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800069 | |||||||
chr5:154800430 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1716+388C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800430 | |||||||
chr5:154800577 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+535A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800577 | |||||||
chr5:154800580 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+538G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800580 | |||||||
chr5:154800581 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+539G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800581 | |||||||
chr5:154800582 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+540A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800582 | |||||||
chr5:154800583 | A | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+541A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800583 | |||||||
chr5:154800584 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+542G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800584 | |||||||
chr5:154800585 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1716+543G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800585 | |||||||
chr5:154800810 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1716+768C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154800810 | |||||||
chr5:154801191 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1717-816T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154801191 | |||||||
chr5:154801557 | C | T | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1717-450C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154801557 | |||||||
chr5:154801799 | T | C | 5 | a0001c0001t0007g0029 a0001c0001t0007g0033 a0001c0001t0007g0069 others(2): Show |
5 | HG00735.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1717-208T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154801799 | |||||||
chr5:154801893 | A | G | 6 | a0001c0001t0003g0045 a0001c0001t0003g0075 a0001c0001t0003g0083 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1717-114A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 10/18 | chr5 | 154801893 | |||||||
chr5:154802431 | C | T | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2109+32C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802431 | |||||||
chr5:154802436 | T | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.2109+37T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802436 | |||||||
chr5:154802523 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0004g0067 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2109+124T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802523 | |||||||
chr5:154802676 | T | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(46): Show |
51 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.2109+277T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802676 | |||||||
chr5:154802714 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2109+315T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802714 | |||||||
chr5:154802909 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02109.hp2 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2110-381G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154802909 | |||||||
chr5:154803005 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2110-285G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154803005 | |||||||
chr5:154803071 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02280.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2110-219G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 11/18 | chr5 | 154803071 | |||||||
chr5:154803452 | G | A | 1 | a0001c0001t0010g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2233+39G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 12/18 | chr5 | 154803452 | |||||||
chr5:154803937 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(69): Show |
76 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.2439+192A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 13/18 | chr5 | 154803937 | |||||||
chr5:154803982 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(31): Show |
36 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.2440-219C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 13/18 | chr5 | 154803982 | |||||||
chr5:154804397 | GA | G | 14 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0173 others(11): Show |
14 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2546+94delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 154804397 | ||||||
chr5:154804401 | A | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0173 others(11): Show |
14 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2546+94A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804401 | |||||||
chr5:154804466 | C | G | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2546+159C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804466 | |||||||
chr5:154804504 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2546+197T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804504 | |||||||
chr5:154804582 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2546+275C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804582 | |||||||
chr5:154804588 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(81): Show |
88 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(85): Show |
intron_variant | MODIFIER | c.2546+281G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804588 | |||||||
chr5:154804603 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2546+296G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804603 | |||||||
chr5:154804772 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2546+465A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804772 | |||||||
chr5:154804903 | T | C | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2546+596T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804903 | |||||||
chr5:154804923 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2546+616C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804923 | |||||||
chr5:154804943 | G | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(74): Show |
81 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(78): Show |
intron_variant | MODIFIER | c.2546+636G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804943 | |||||||
chr5:154804945 | T | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.2546+638T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154804945 | |||||||
chr5:154805003 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0236 a0001c0001t0001g0238 others(13): Show |
18 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2546+696A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805003 | |||||||
chr5:154805011 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2546+704T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805011 | |||||||
chr5:154805111 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
6 | HG02109.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2547-770C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805111 | |||||||
chr5:154805171 | G | T | 10 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0125 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2547-710G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805171 | |||||||
chr5:154805230 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
8 | HG02109.hp2 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2547-651A>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805230 | |||||||
chr5:154805312 | T | TAGCAGGC others(83): Show |
5 | a0001c0001t0001g0239 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02165.hp1 HG02293.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2547-537_2547-448d others(92): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 154805312 | ||||||
chr5:154805312 | T | TAGCAGGC others(173): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0241 a0001c0001t0001g0244 others(3): Show |
8 | HG02056.hp2 HG02129.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.2547-448_2547-447i others(182): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 154805312 | ||||||
chr5:154805312 | T | TAGCAGGC others(263): Show |
1 | a0001c0001t0014g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2547-448_2547-447i others(272): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 154805312 | ||||||
chr5:154805312 | TAGCAGGC others(83): Show |
T | 1 | a0001c0001t0001g0268 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2547-537_2547-448d others(92): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr5 | 154805312 | ||||||
chr5:154805349 | G | C | 1 | a0001c0001t0004g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2547-532G>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805349 | |||||||
chr5:154805716 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2547-165A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 14/18 | chr5 | 154805716 | |||||||
chr5:154806066 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2698+34G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806066 | |||||||
chr5:154806119 | ACTCTTTT | A | 8 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0050 others(5): Show |
8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2698+92_2698+98del others(7): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 154806119 | ||||||
chr5:154806139 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2698+107A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806139 | |||||||
chr5:154806171 | A | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(69): Show |
76 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(73): Show |
intron_variant | MODIFIER | c.2698+139A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806171 | |||||||
chr5:154806188 | G | A | 13 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(10): Show |
14 | HG01952.hp2 HG01978.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.2698+156G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806188 | |||||||
chr5:154806239 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2698+207C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806239 | |||||||
chr5:154806343 | A | C | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2698+311A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806343 | |||||||
chr5:154806654 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2698+622T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806654 | |||||||
chr5:154806712 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2698+680A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806712 | |||||||
chr5:154806742 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2698+710T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154806742 | |||||||
chr5:154807201 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2698+1169C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807201 | |||||||
chr5:154807618 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2699-841A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807618 | |||||||
chr5:154807743 | G | A | 1 | a0001c0001t0006g0131 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2699-716G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807743 | |||||||
chr5:154807884 | A | G | 7 | a0001c0001t0006g0110 a0001c0001t0006g0111 a0001c0001t0006g0126 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2699-575A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807884 | |||||||
chr5:154807909 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2699-550T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807909 | |||||||
chr5:154807918 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2699-541C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154807918 | |||||||
chr5:154808037 | T | G | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2699-422T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154808037 | |||||||
chr5:154808123 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2699-336T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154808123 | |||||||
chr5:154808186 | C | A | 1 | a0001c0001t0001g0005 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2699-273C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154808186 | |||||||
chr5:154808325 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2699-134G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154808325 | |||||||
chr5:154808447 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2699-12C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 15/18 | chr5 | 154808447 | |||||||
chr5:154808654 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2843+51G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154808654 | |||||||
chr5:154808887 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2843+284G>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154808887 | |||||||
chr5:154809117 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0026 others(2): Show |
6 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2843+514T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809117 | |||||||
chr5:154809171 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2843+568T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809171 | |||||||
chr5:154809217 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2843+614C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809217 | |||||||
chr5:154809240 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2843+637G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809240 | |||||||
chr5:154809287 | C | T | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2843+684C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809287 | |||||||
chr5:154809384 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0140 others(9): Show |
12 | HG00558.hp2 HG00621.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2843+781C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809384 | |||||||
chr5:154809493 | A | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG00140.hp2 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.2843+890A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809493 | |||||||
chr5:154809699 | C | CT | 8 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0163 others(5): Show |
8 | HG02300.hp2 HG02976.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.2843+1114dupT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr5 | 154809699 | ||||||
chr5:154809798 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2843+1195C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809798 | |||||||
chr5:154809850 | C | G | 1 | a0001c0001t0009g0136 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2843+1247C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809850 | |||||||
chr5:154809862 | C | T | 1 | a0001c0003t0001g0042 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2843+1259C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809862 | |||||||
chr5:154809997 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2844-1250C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154809997 | |||||||
chr5:154810013 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2844-1234T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810013 | |||||||
chr5:154810019 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2844-1228C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810019 | |||||||
chr5:154810083 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0004g0067 |
2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2844-1164G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810083 | |||||||
chr5:154810341 | T | C | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.2844-906T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810341 | |||||||
chr5:154810368 | A | G | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0016 others(43): Show |
49 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.2844-879A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810368 | |||||||
chr5:154810427 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2844-820C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810427 | |||||||
chr5:154810428 | T | G | 77 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.2844-819T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810428 | |||||||
chr5:154810466 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2844-781A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810466 | |||||||
chr5:154810490 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2844-757T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810490 | |||||||
chr5:154810621 | G | A | 1 | a0001c0001t0006g0126 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2844-626G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810621 | |||||||
chr5:154810650 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2844-597G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810650 | |||||||
chr5:154810786 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2844-461C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810786 | |||||||
chr5:154810962 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2844-285C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810962 | |||||||
chr5:154810963 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0236 a0001c0001t0001g0238 others(13): Show |
18 | HG00323.hp1 HG00609.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2844-284G>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154810963 | |||||||
chr5:154811130 | T | C | 1 | a0004c0009t0017g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2844-117T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 16/18 | chr5 | 154811130 | |||||||
chr5:154811501 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2954-12C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 17/18 | chr5 | 154811501 | |||||||
chr5:154811993 | C | T | 2 | a0001c0001t0013g0064 a0001c0001t0013g0079 |
2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.3081+353C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154811993 | |||||||
chr5:154812003 | T | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02559.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3081+363T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812003 | |||||||
chr5:154812169 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3081+529A>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812169 | |||||||
chr5:154812505 | GC | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(132): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.3081+877delC | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154812505 | ||||||
chr5:154812505 | GCC | G | 39 | a0001c0001t0001g0036 a0001c0001t0001g0094 a0001c0001t0001g0103 others(36): Show |
40 | HG00558.hp1 HG00642.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.3081+876_3081+877d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154812505 | ||||||
chr5:154812505 | GCCC | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
35 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.3081+875_3081+877d others(5): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154812505 | ||||||
chr5:154812516 | C | A | 1 | a0001c0003t0001g0052 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3081+876C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812516 | |||||||
chr5:154812517 | C | A | 12 | a0001c0001t0001g0068 a0001c0001t0001g0157 a0001c0001t0004g0067 others(9): Show |
12 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.3081+877C>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812517 | |||||||
chr5:154812517 | C | G | 1 | a0001c0002t0002g0162 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3081+877C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812517 | |||||||
chr5:154812518 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3081+878A>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812518 | |||||||
chr5:154812525 | CT | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0025 others(2): Show |
6 | HG02486.hp1 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3081+896delT | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154812525 | ||||||
chr5:154812525 | CTT | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(30): Show |
35 | HG00597.hp2 HG01081.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.3081+895_3081+896d others(4): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154812525 | ||||||
chr5:154812587 | T | G | 4 | a0001c0001t0009g0136 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG00558.hp1 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3081+947T>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812587 | |||||||
chr5:154812612 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3081+972C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812612 | |||||||
chr5:154812660 | TA | T | 5 | a0001c0001t0007g0029 a0001c0001t0007g0033 a0001c0001t0007g0069 others(2): Show |
5 | HG00735.hp2 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3081+1021delA | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812660 | |||||||
chr5:154812676 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3081+1036C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812676 | |||||||
chr5:154812828 | T | A | 1 | a0001c0001t0001g0276 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3082-1059T>A | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812828 | |||||||
chr5:154812888 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3082-999C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812888 | |||||||
chr5:154812911 | C | T | 2 | a0001c0002t0001g0200 a0001c0002t0001g0223 |
2 | HG03834.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-976C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154812911 | |||||||
chr5:154813022 | T | C | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0005g0113 others(22): Show |
26 | HG01243.hp2 HG01891.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.3082-865T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154813022 | |||||||
chr5:154813100 | T | C | 1 | a0001c0003t0001g0116 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3082-787T>C | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154813100 | |||||||
chr5:154813100 | T | TAGAC | 238 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.3082-785_3082-784i others(6): Show |
LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 154813100 | ||||||
chr5:154813268 | C | T | 1 | a0001c0001t0016g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3082-619C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154813268 | |||||||
chr5:154813692 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3082-195C>G | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154813692 | |||||||
chr5:154813841 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0041 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3082-46C>T | LARP1 | ENSG00000155506.19 | transcript | ENST00000518297.6 | protein_coding | 18/18 | chr5 | 154813841 |