Item | Value |
---|---|
geneid | 57142 |
ensemblid | ENSG00000115310.19 |
hgncid | 14085 |
symbol | RTN4 |
name | reticulon 4 |
refseq_nuc | NM_020532.5 |
refseq_prot | NP_065393.1 |
ensembl_nuc | ENST00000337526.11 |
ensembl_prot | ENSP00000337838.6 |
mane_status | MANE Select |
chr | chr2 |
start | 54972189 |
end | 55050451 |
strand | - |
ver | v1.2 |
region | chr2:54972189-55050451 |
region5000 | chr2:54967189-55055451 |
regionname0 | RTN4_chr2_54972189_55050451 |
regionname5000 | RTN4_chr2_54967189_55055451 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1192 | 254 | 65 | 35 | 110 | 13 | 29 | 92 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0002 | 0/0 | 1192 | 49 | 1 | 18 | 21 | 1 | 8 | 17 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0003 | 0/0 | 1192 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0004 | 0/0 | 1192 | 8 | 0 | 2 | 5 | 1 | 0 | 4 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0005 | 0/0 | 1192 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0006 | 0/0 | 1192 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0007 | 0/0 | 1192 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0008 | 0/0 | 1192 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0009 | 0/0 | 1192 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0010 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0011 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0012 | 0/0 | 1192 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0013 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0014 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0015 | 0/0 | 1114 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MDFGN others(1109): Show |
chr2 | 54967189 | 55055451 |
a0016 | 0/0 | 1192 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
a0017 | 0/0 | 1192 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | MEDLD others(1187): Show |
chr2 | 54967189 | 55055451 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3576 | 243 | 59 | 31 | 109 | 13 | 29 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0008 | 0/0 | 3576 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0010 | 0/0 | 3576 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0012 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0013 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0017 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0021 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0001c0023 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0002c0002 | 0/0 | 3576 | 48 | 1 | 17 | 21 | 1 | 8 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0002c0011 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0003c0003 | 0/0 | 3576 | 9 | 9 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0004c0004 | 0/0 | 3576 | 8 | 0 | 2 | 5 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0005c0005 | 0/0 | 3576 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0006c0006 | 0/0 | 3576 | 6 | 5 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0007c0007 | 0/0 | 3576 | 5 | 4 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0008c0009 | 0/0 | 3576 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0009c0022 | 0/0 | 3576 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0010c0024 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0011c0015 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0012c0020 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0013c0014 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0014c0018 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0015c0025 | 0/0 | 3576 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | GGGGT others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0016c0019 | 0/0 | 3576 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 | ||
a0017c0016 | 0/0 | 3576 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATGGA others(3571): Show |
chr2 | 54967189 | 55055451 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4697 | 95 | 12 | 14 | 49 | 7 | 12 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0002 | 0/1 | 4696 | 77 | 3 | 11 | 52 | 5 | 5 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0003 | 0/0 | 4698 | 5 | 0 | 0 | 5 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0004 | 0/0 | 4698 | 17 | 15 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0005 | 0/0 | 4693 | 26 | 13 | 3 | 0 | 1 | 9 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4688): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0006 | 0/0 | 4693 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4688): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0007 | 0/0 | 4698 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0009 | 0/0 | 4698 | 4 | 4 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0011 | 0/0 | 4700 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4695): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0012 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0014 | 0/0 | 4696 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0016 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0020 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4696): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0021 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0023 | 0/0 | 4696 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0001c0001t0024 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0008t0008 | 0/0 | 4698 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0008t0017 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4695): Show |
chr2 | 54967189 | 55055451 |
a0001c0010t0002 | 0/0 | 4696 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0001c0012t0004 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0013t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0017t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0001c0021t0007 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0001c0023t0001 | 0/0 | 4697 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0002c0002t0001 | 0/0 | 4697 | 2 | 0 | 1 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0002c0002t0002 | 0/0 | 4696 | 4 | 0 | 0 | 4 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0002c0002t0003 | 0/0 | 4698 | 38 | 1 | 16 | 14 | 1 | 6 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0002c0002t0010 | 0/0 | 4702 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4697): Show |
chr2 | 54967189 | 55055451 |
a0002c0002t0018 | 0/0 | 4698 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0002c0011t0003 | 0/0 | 4698 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0003c0003t0004 | 0/0 | 4698 | 7 | 7 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0003c0003t0013 | 0/0 | 4698 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0004c0004t0002 | 0/0 | 4696 | 8 | 0 | 2 | 5 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0005c0005t0001 | 0/0 | 4697 | 8 | 8 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0006c0006t0002 | 0/0 | 4696 | 5 | 4 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0006c0006t0022 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0007c0007t0004 | 0/0 | 4698 | 3 | 3 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0007c0007t0012 | 0/0 | 4697 | 2 | 1 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0008c0009t0001 | 0/0 | 4697 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0009c0022t0001 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0010c0024t0006 | 0/0 | 4693 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4688): Show |
chr2 | 54967189 | 55055451 |
a0011c0015t0008 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4693): Show |
chr2 | 54967189 | 55055451 |
a0012c0020t0002 | 0/0 | 4696 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4691): Show |
chr2 | 54967189 | 55055451 |
a0013c0014t0001 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0014c0018t0019 | 0/0 | 4700 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4695): Show |
chr2 | 54967189 | 55055451 |
a0015c0025t0015 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ACTGG others(4692): Show |
chr2 | 54967189 | 55055451 |
a0016c0019t0001 | 0/0 | 4697 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
a0017c0016t0001 | 0/0 | 4697 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | ATTGT others(4692): Show |
chr2 | 54967189 | 55055451 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0006g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0009g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0009g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0011g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0014g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0014g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0020g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0021g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0023g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0001t0024g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0008t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0008t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0008t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0008t0017g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0010t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0010t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0012t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0013t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0017t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0021t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0001c0023t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0010g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0010g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0002t0018g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0002c0011t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0003c0003t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0004c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0005c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0006c0006t0002g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0006c0006t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0006c0006t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0006c0006t0022g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0007c0007t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0007c0007t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0007c0007t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0007c0007t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0007c0007t0012g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0008c0009t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0008c0009t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0009c0022t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0010c0024t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0011c0015t0008g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0012c0020t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0013c0014t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0014c0018t0019g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0015c0025t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0016c0019t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
a0017c0016t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0290 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0178 | EUR | GBR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0132 | EUR | FIN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00544 | hp2 | a0002 | c0002 | t0003 | g0020 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00558 | hp2 | a0008 | c0009 | t0001 | g0106 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0054 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00735 | hp1 | a0002 | c0002 | t0003 | g0040 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00738 | hp1 | a0006 | c0006 | t0002 | g0003 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0037 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01070 | hp1 | a0002 | c0002 | t0003 | g0051 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01070 | hp2 | a0004 | c0004 | t0002 | g0009 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0287 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01071 | hp2 | a0004 | c0004 | t0002 | g0009 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01167 | hp1 | a0007 | c0007 | t0012 | g0065 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0061 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01168 | hp2 | a0002 | c0002 | t0003 | g0035 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01256 | hp1 | a0001 | c0010 | t0002 | g0320 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0013 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01257 | hp2 | a0009 | c0022 | t0001 | g0319 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01258 | hp1 | a0001 | c0010 | t0002 | g0321 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0017 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0048 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01496 | hp1 | a0001 | c0017 | t0001 | g0265 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01496 | hp2 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01515 | hp1 | a0004 | c0004 | t0002 | g0137 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0024 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0080 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01891 | hp2 | a0003 | c0003 | t0004 | g0004 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01943 | hp2 | a0002 | c0011 | t0003 | g0046 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01952 | hp1 | a0001 | c0001 | t0023 | g0150 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0016 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0036 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01981 | hp1 | a0002 | c0002 | t0003 | g0038 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02055 | hp2 | a0001 | c0001 | t0020 | g0118 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02083 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02132 | hp2 | a0001 | c0001 | t0011 | g0267 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0032 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0303 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0306 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0041 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02451 | hp2 | a0007 | c0007 | t0004 | g0066 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02523 | hp1 | a0002 | c0002 | t0003 | g0021 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02523 | hp2 | a0004 | c0004 | t0002 | g0191 | EAS | KHV | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02572 | hp1 | a0003 | c0003 | t0004 | g0073 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02615 | hp1 | a0010 | c0024 | t0006 | g0331 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0299 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0333 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0050 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02698 | hp2 | a0002 | c0002 | t0003 | g0031 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02717 | hp2 | a0003 | c0003 | t0004 | g0005 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0330 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0286 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02809 | hp1 | a0001 | c0008 | t0017 | g0067 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0298 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02818 | hp1 | a0005 | c0005 | t0001 | g0325 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02818 | hp2 | a0001 | c0008 | t0008 | g0261 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02886 | hp1 | a0006 | c0006 | t0002 | g0003 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02886 | hp2 | a0001 | c0008 | t0008 | g0259 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02895 | hp1 | a0003 | c0003 | t0004 | g0318 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02895 | hp2 | a0011 | c0015 | t0008 | g0308 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02896 | hp1 | a0005 | c0005 | t0001 | g0324 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0316 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02897 | hp1 | a0005 | c0005 | t0001 | g0326 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02897 | hp2 | a0003 | c0003 | t0004 | g0317 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02922 | hp1 | a0006 | c0006 | t0002 | g0302 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02922 | hp2 | a0003 | c0003 | t0004 | g0005 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0309 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02970 | hp2 | a0001 | c0021 | t0007 | g0336 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03017 | hp2 | a0002 | c0002 | t0003 | g0055 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03130 | hp2 | a0007 | c0007 | t0004 | g0062 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0164 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03195 | hp2 | a0001 | c0001 | t0016 | g0313 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03209 | hp2 | a0003 | c0003 | t0004 | g0004 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03225 | hp2 | a0005 | c0005 | t0001 | g0329 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03239 | hp1 | a0002 | c0002 | t0003 | g0057 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03453 | hp1 | a0006 | c0006 | t0002 | g0003 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0293 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0335 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03486 | hp2 | a0001 | c0008 | t0008 | g0260 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03491 | hp2 | a0002 | c0002 | t0018 | g0023 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03516 | hp1 | a0012 | c0020 | t0002 | g0315 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03516 | hp2 | a0003 | c0003 | t0013 | g0071 | AFR | ESN | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0327 | AFR | GWD | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0334 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03654 | hp1 | a0001 | c0001 | t0014 | g0254 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0282 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03704 | hp2 | a0002 | c0002 | t0003 | g0052 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03710 | hp1 | a0001 | c0001 | t0021 | g0221 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0281 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04184 | hp1 | a0001 | c0001 | t0014 | g0146 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04184 | hp2 | a0002 | c0002 | t0003 | g0053 | SAS | BEB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG04228 | hp2 | a0013 | c0014 | t0001 | g0244 | SAS | STU | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18522 | hp2 | a0006 | c0006 | t0002 | g0301 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0027 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0019 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18960 | hp2 | a0002 | c0002 | t0003 | g0028 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18972 | hp1 | a0002 | c0002 | t0003 | g0026 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18974 | hp1 | a0004 | c0004 | t0002 | g0168 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18985 | hp1 | a0014 | c0018 | t0019 | g0160 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18985 | hp2 | a0002 | c0002 | t0003 | g0045 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18986 | hp1 | a0001 | c0001 | t0011 | g0264 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18989 | hp2 | a0002 | c0002 | t0003 | g0042 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18990 | hp2 | a0004 | c0004 | t0002 | g0166 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18992 | hp1 | a0002 | c0002 | t0010 | g0018 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18993 | hp2 | a0002 | c0002 | t0010 | g0043 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18999 | hp1 | a0001 | c0001 | t0011 | g0268 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19003 | hp1 | a0002 | c0002 | t0003 | g0029 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0030 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19030 | hp2 | a0015 | c0025 | t0015 | g0012 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0279 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0217 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19055 | hp2 | a0001 | c0023 | t0001 | g0322 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19056 | hp1 | a0016 | c0019 | t0001 | g0269 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19057 | hp1 | a0004 | c0004 | t0002 | g0165 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19058 | hp1 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19082 | hp1 | a0008 | c0009 | t0001 | g0105 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19082 | hp2 | a0002 | c0002 | t0010 | g0034 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19086 | hp1 | a0004 | c0004 | t0002 | g0167 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA19240 | hp2 | a0005 | c0005 | t0001 | g0328 | AFR | YRI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20129 | hp1 | a0001 | c0012 | t0004 | g0213 | AFR | ASW | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0332 | AFR | ASW | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20752 | hp2 | a0017 | c0016 | t0001 | g0107 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | TSI | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0284 | SAS | GIH | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01123 | hp1 | a0001 | c0013 | t0001 | g0122 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0291 | AMR | CLM | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02109 | hp1 | a0005 | c0005 | t0001 | g0323 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02559 | hp1 | a0007 | c0007 | t0004 | g0063 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0192 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG03471 | hp2 | a0006 | c0006 | t0022 | g0305 | AFR | MSL | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG06807 | hp1 | a0007 | c0007 | t0012 | g0064 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | USA | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA21309 | hp1 | a0003 | c0003 | t0013 | g0072 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | LWK | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0144 | REF | REF | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0245 | REF | REF | RTN4_chr2_54967189_55055451 | RTN4 | chr2 | 54967189 | 55055451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:54973197 | T | A | 1 | a0014 | 1 | NA18985.hp1 | missense_variant&splice_region_variant | MODERATE | c.3538A>T | p.Ile1180Phe | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 3689/4697 | 3538/3579 | 1180/1192 | chr2 | 54973197 | |||
chr2:54982570 | G | A | 1 | a0016 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.3305C>T | p.Thr1102Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/9 | 3456/4697 | 3305/3579 | 1102/1192 | chr2 | 54982570 | |||
chr2:54982630 | G | C | 1 | a0012 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.3245C>G | p.Ala1082Gly | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/9 | 3396/4697 | 3245/3579 | 1082/1192 | chr2 | 54982630 | |||
chr2:55025328 | A | G | 1 | a0006 | 6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
missense_variant | MODERATE | c.2771T>C | p.Ile924Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2922/4697 | 2771/3579 | 924/1192 | chr2 | 55025328 | |||
chr2:55025340 | G | C | 1 | a0003 | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
missense_variant | MODERATE | c.2759C>G | p.Ser920Cys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2910/4697 | 2759/3579 | 920/1192 | chr2 | 55025340 | |||
chr2:55025404 | C | G | 1 | a0003 | 9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
missense_variant | MODERATE | c.2695G>C | p.Glu899Gln | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2846/4697 | 2695/3579 | 899/1192 | chr2 | 55025404 | |||
chr2:55025659 | G | T | 1 | a0017 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.2440C>A | p.Leu814Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2591/4697 | 2440/3579 | 814/1192 | chr2 | 55025659 | |||
chr2:55025743 | C | T | 1 | a0011 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.2356G>A | p.Glu786Lys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2507/4697 | 2356/3579 | 786/1192 | chr2 | 55025743 | |||
chr2:55025808 | A | T | 1 | a0013 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2291T>A | p.Val764Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2442/4697 | 2291/3579 | 764/1192 | chr2 | 55025808 | |||
chr2:55026750 | G | A | 2 | a0005 a0015 |
9 | HG02109.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.1349C>T | p.Thr450Met | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1500/4697 | 1349/3579 | 450/1192 | chr2 | 55026750 | |||
chr2:55026924 | C | T | 1 | a0007 | 5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
missense_variant | MODERATE | c.1175G>A | p.Arg392Gln | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1326/4697 | 1175/3579 | 392/1192 | chr2 | 55026924 | |||
chr2:55026960 | A | G | 1 | a0008 | 2 | HG00558.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.1139T>C | p.Met380Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1290/4697 | 1139/3579 | 380/1192 | chr2 | 55026960 | |||
chr2:55027029 | T | A | 1 | a0004 | 8 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(5): Show |
missense_variant | MODERATE | c.1070A>T | p.Asp357Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1221/4697 | 1070/3579 | 357/1192 | chr2 | 55027029 | |||
chr2:55049968 | G | C | 1 | a0009 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.333C>G | p.Ser111Arg | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 484/4697 | 333/3579 | 111/1192 | chr2 | 55049968 | |||
chr2:55050072 | G | C | 3 | a0005 a0010 a0015 |
10 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
missense_variant | MODERATE | c.229C>G | p.Pro77Ala | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 380/4697 | 229/3579 | 77/1192 | chr2 | 55050072 | |||
chr2:55050090 | C | T | 1 | a0002 | 49 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(46): Show |
missense_variant | MODERATE | c.211G>A | p.Ala71Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 362/4697 | 211/3579 | 71/1192 | chr2 | 55050090 | |||
chr2:55050178 | T | G | 1 | a0010 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.123A>C | p.Glu41Asp | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 274/4697 | 123/3579 | 41/1192 | chr2 | 55050178 | |||
chr2:55050282 | A | T | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.19T>A | p.Ser7Thr | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 170/4697 | 19/3579 | 7/1192 | chr2 | 55050282 | |||
chr2:55050285 | G | C | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.16C>G | p.Gln6Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 167/4697 | 16/3579 | 6/1192 | chr2 | 55050285 | |||
chr2:55050290 | A | C | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.11T>G | p.Leu4Arg | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 162/4697 | 11/3579 | 4/1192 | chr2 | 55050290 | |||
chr2:55050293 | T | C | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.8A>G | p.Asp3Gly | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 159/4697 | 8/3579 | 3/1192 | chr2 | 55050293 | |||
chr2:55050296 | T | A | 1 | a0015 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.5A>T | p.Glu2Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 156/4697 | 5/3579 | 2/1192 | chr2 | 55050296 | |||
chr2:55050299 | A | C | 1 | a0015 | 1 | NA19030.hp2 | start_lost | HIGH | c.2T>G | p.Met1? | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 153/4697 | 2/3579 | 1/1192 | chr2 | 55050299 | |||
chr2:55050300 | T | C | 1 | a0015 | 1 | NA19030.hp2 | start_lost | HIGH | c.1A>G | p.Met1? | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 152/4697 | 1/3579 | 1/1192 | chr2 | 55050300 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55025123 | T | C | 2 | a0001c0008 a0011c0015 |
5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.2976A>G | p.Pro992Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 3127/4697 | 2976/3579 | 992/1192 | chr2 | 55025123 | |||
chr2:55025330 | G | A | 1 | a0001c0021 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2769C>T | p.Asn923Asn | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2920/4697 | 2769/3579 | 923/1192 | chr2 | 55025330 | |||
chr2:55025387 | C | T | 1 | a0001c0017 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.2712G>A | p.Pro904Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2863/4697 | 2712/3579 | 904/1192 | chr2 | 55025387 | |||
chr2:55025408 | T | C | 1 | a0002c0011 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.2691A>G | p.Lys897Lys | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2842/4697 | 2691/3579 | 897/1192 | chr2 | 55025408 | |||
chr2:55026241 | A | G | 2 | a0001c0012 a0007c0007 |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.1858T>C | p.Leu620Leu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 2009/4697 | 1858/3579 | 620/1192 | chr2 | 55026241 | |||
chr2:55026911 | C | T | 1 | a0001c0013 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.1188G>A | p.Val396Val | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/9 | 1339/4697 | 1188/3579 | 396/1192 | chr2 | 55026911 | |||
chr2:55028219 | A | G | 1 | a0001c0012 | 1 | NA20129.hp1 | splice_region_variant&synonymous_variant | LOW | c.558T>C | p.Asp186Asp | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/9 | 709/4697 | 558/3579 | 186/1192 | chr2 | 55028219 | |||
chr2:55050007 | G | C | 1 | a0001c0010 | 2 | HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.294C>G | p.Pro98Pro | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 445/4697 | 294/3579 | 98/1192 | chr2 | 55050007 | |||
chr2:55050034 | C | A | 1 | a0001c0023 | 1 | NA19055.hp2 | synonymous_variant | LOW | c.267G>T | p.Ala89Ala | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 418/4697 | 267/3579 | 89/1192 | chr2 | 55050034 | |||
chr2:55050280 | A | G | 1 | a0015c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.21T>C | p.Ser7Ser | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 172/4697 | 21/3579 | 7/1192 | chr2 | 55050280 | |||
chr2:55050291 | G | A | 1 | a0015c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.10C>T | p.Leu4Leu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 161/4697 | 10/3579 | 4/1192 | chr2 | 55050291 | |||
chr2:55050295 | T | C | 1 | a0015c0025 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.6A>G | p.Glu2Glu | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 157/4697 | 6/3579 | 2/1192 | chr2 | 55050295 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:54972306 | T | A | 8 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0016 others(5): Show |
34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*850A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 850 | chr2 | 54972306 | ||||||
chr2:54972320 | A | ATGTT | 2 | a0001c0001t0020 a0002c0002t0010 |
4 | HG02055.hp2 NA18992.hp1 NA18993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*832_*835dupAACA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 835 | chr2 | 54972320 | ||||||
chr2:54972363 | A | G | 1 | a0001c0008t0017 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 793 | chr2 | 54972363 | ||||||
chr2:54972374 | A | C | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0021t0007 |
9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*782T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 782 | chr2 | 54972374 | ||||||
chr2:54972380 | T | A | 1 | a0014c0018t0019 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 776 | chr2 | 54972380 | ||||||
chr2:54972421 | A | ATGT | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0014 others(9): Show |
105 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*732_*734dupACA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 734 | chr2 | 54972421 | ||||||
chr2:54972464 | T | C | 1 | a0001c0001t0021 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*692A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 692 | chr2 | 54972464 | ||||||
chr2:54972628 | T | C | 3 | a0001c0008t0008 a0001c0008t0017 a0011c0015t0008 |
5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*528A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 528 | chr2 | 54972628 | ||||||
chr2:54972707 | C | T | 1 | a0002c0002t0018 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 449 | chr2 | 54972707 | ||||||
chr2:54972712 | T | C | 2 | a0001c0001t0006 a0010c0024t0006 |
5 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*444A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 444 | chr2 | 54972712 | ||||||
chr2:54972795 | C | CT | 17 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(14): Show |
93 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*360dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 360 | chr2 | 54972795 | ||||||
chr2:54972819 | C | A | 1 | a0001c0001t0023 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 337 | chr2 | 54972819 | ||||||
chr2:54972902 | CAGAT | C | 12 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(9): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*250_*253delATCT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 250 | chr2 | 54972902 | ||||||
chr2:54972905 | A | ATAGAT | 1 | a0001c0001t0001 | 3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*246_*250dupATCTA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 250 | chr2 | 54972905 | ||||||
chr2:54972929 | C | A | 1 | a0001c0001t0024 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*227G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 227 | chr2 | 54972929 | ||||||
chr2:54972945 | A | G | 3 | a0001c0008t0008 a0001c0008t0017 a0011c0015t0008 |
5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*211T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 211 | chr2 | 54972945 | ||||||
chr2:54972968 | T | A | 1 | a0003c0003t0013 | 2 | HG03516.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*188A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 188 | chr2 | 54972968 | ||||||
chr2:54972986 | C | A | 1 | a0001c0001t0016 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*170G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 170 | chr2 | 54972986 | ||||||
chr2:54972989 | G | T | 1 | a0001c0001t0016 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 167 | chr2 | 54972989 | ||||||
chr2:54973086 | G | C | 1 | a0001c0001t0014 | 2 | HG03654.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*70C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 9/9 | 70 | chr2 | 54973086 | ||||||
chr2:55050304 | T | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 4 | chr2 | 55050304 | ||||||
chr2:55050306 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-6C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050306 | |||||||
chr2:55050310 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 10 | chr2 | 55050310 | ||||||
chr2:55050311 | T | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 11 | chr2 | 55050311 | ||||||
chr2:55050312 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-12C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 12 | chr2 | 55050312 | ||||||
chr2:55050314 | A | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 14 | chr2 | 55050314 | ||||||
chr2:55050316 | A | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 16 | chr2 | 55050316 | ||||||
chr2:55050318 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050318 | |||||||
chr2:55050320 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 20 | chr2 | 55050320 | ||||||
chr2:55050322 | C | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 22 | chr2 | 55050322 | ||||||
chr2:55050323 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-23A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050323 | |||||||
chr2:55050324 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 24 | chr2 | 55050324 | ||||||
chr2:55050328 | C | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 28 | chr2 | 55050328 | ||||||
chr2:55050330 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 30 | chr2 | 55050330 | ||||||
chr2:55050331 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 31 | chr2 | 55050331 | ||||||
chr2:55050334 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 34 | chr2 | 55050334 | ||||||
chr2:55050335 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 35 | chr2 | 55050335 | ||||||
chr2:55050337 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 37 | chr2 | 55050337 | ||||||
chr2:55050338 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050338 | |||||||
chr2:55050346 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 46 | chr2 | 55050346 | ||||||
chr2:55050349 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 49 | chr2 | 55050349 | ||||||
chr2:55050352 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 52 | chr2 | 55050352 | ||||||
chr2:55050354 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 54 | chr2 | 55050354 | ||||||
chr2:55050355 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 55 | chr2 | 55050355 | ||||||
chr2:55050356 | T | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 56 | chr2 | 55050356 | ||||||
chr2:55050357 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 57 | chr2 | 55050357 | ||||||
chr2:55050361 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 61 | chr2 | 55050361 | ||||||
chr2:55050362 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 62 | chr2 | 55050362 | ||||||
chr2:55050363 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050363 | |||||||
chr2:55050365 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 65 | chr2 | 55050365 | ||||||
chr2:55050366 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050366 | |||||||
chr2:55050369 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-69G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 69 | chr2 | 55050369 | ||||||
chr2:55050372 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-72A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 72 | chr2 | 55050372 | ||||||
chr2:55050373 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-73A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 73 | chr2 | 55050373 | ||||||
chr2:55050375 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 75 | chr2 | 55050375 | ||||||
chr2:55050378 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 78 | chr2 | 55050378 | ||||||
chr2:55050381 | T | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 81 | chr2 | 55050381 | ||||||
chr2:55050382 | T | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 82 | chr2 | 55050382 | ||||||
chr2:55050384 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 84 | chr2 | 55050384 | ||||||
chr2:55050388 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 88 | chr2 | 55050388 | ||||||
chr2:55050399 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-99C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 99 | chr2 | 55050399 | ||||||
chr2:55050401 | C | A | 2 | a0001c0001t0007 a0001c0021t0007 |
5 | HG02647.hp2 HG02970.hp2 HG03486.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-101G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 101 | chr2 | 55050401 | ||||||
chr2:55050406 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-106G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 106 | chr2 | 55050406 | ||||||
chr2:55050407 | C | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 107 | chr2 | 55050407 | ||||||
chr2:55050409 | A | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-109T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 109 | chr2 | 55050409 | ||||||
chr2:55050410 | C | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-110G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 110 | chr2 | 55050410 | ||||||
chr2:55050411 | T | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-111A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 111 | chr2 | 55050411 | ||||||
chr2:55050415 | C | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 115 | chr2 | 55050415 | ||||||
chr2:55050416 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 116 | chr2 | 55050416 | ||||||
chr2:55050419 | G | A | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-119C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 119 | chr2 | 55050419 | ||||||
chr2:55050421 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 121 | chr2 | 55050421 | ||||||
chr2:55050422 | A | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-122T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 122 | chr2 | 55050422 | ||||||
chr2:55050425 | T | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-125A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 125 | chr2 | 55050425 | ||||||
chr2:55050426 | A | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 126 | chr2 | 55050426 | ||||||
chr2:55050428 | T | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 128 | chr2 | 55050428 | ||||||
chr2:55050430 | T | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 130 | chr2 | 55050430 | ||||||
chr2:55050432 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-132C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 132 | chr2 | 55050432 | ||||||
chr2:55050435 | A | T | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-135T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 135 | chr2 | 55050435 | ||||||
chr2:55050437 | G | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 137 | chr2 | 55050437 | ||||||
chr2:55050440 | T | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-140A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 140 | chr2 | 55050440 | ||||||
chr2:55050441 | C | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-141G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 141 | chr2 | 55050441 | ||||||
chr2:55050447 | A | C | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | 147 | chr2 | 55050447 | ||||||
chr2:55050450 | A | G | 1 | a0015c0025t0015 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-150T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/9 | chr2 | 55050450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:54973648 | T | G | 1 | a0001c0001t0001g0250 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3478-27A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973648 | |||||||
chr2:54973664 | T | G | 90 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(87): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.3478-43A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973664 | |||||||
chr2:54973759 | G | A | 1 | a0001c0001t0023g0150 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3477+62C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 7/8 | chr2 | 54973759 | |||||||
chr2:54973902 | C | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(245): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.3431-35G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54973902 | |||||||
chr2:54973980 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3431-113T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54973980 | |||||||
chr2:54974113 | A | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3431-246T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974113 | |||||||
chr2:54974225 | G | C | 8 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(5): Show |
8 | HG02647.hp2 HG02896.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3431-358C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974225 | |||||||
chr2:54974285 | C | T | 5 | a0002c0002t0001g0049 a0002c0002t0003g0050 a0002c0002t0003g0051 others(2): Show |
5 | HG01070.hp1 HG02683.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.3430+410G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974285 | |||||||
chr2:54974340 | C | G | 1 | a0001c0001t0006g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3430+355G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974340 | |||||||
chr2:54974560 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3430+135G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974560 | |||||||
chr2:54974592 | C | T | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3430+103G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 6/8 | chr2 | 54974592 | |||||||
chr2:54974863 | G | C | 1 | a0004c0004t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3361-99C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54974863 | |||||||
chr2:54974863 | G | T | 2 | a0001c0001t0003g0130 a0001c0001t0003g0131 |
2 | NA18954.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.3361-99C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54974863 | |||||||
chr2:54975120 | T | G | 1 | a0002c0002t0003g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3361-356A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975120 | |||||||
chr2:54975319 | G | A | 57 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(54): Show |
60 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.3361-555C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975319 | |||||||
chr2:54975343 | C | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3361-579G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975343 | |||||||
chr2:54975369 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3361-605A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975369 | |||||||
chr2:54975401 | C | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3361-637G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975401 | |||||||
chr2:54975503 | T | C | 3 | a0003c0003t0004g0004 a0003c0003t0013g0071 a0003c0003t0013g0072 |
4 | HG01891.hp2 HG03209.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-739A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975503 | |||||||
chr2:54975513 | C | T | 247 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(244): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.3361-749G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975513 | |||||||
chr2:54975624 | A | G | 4 | a0001c0001t0002g0174 a0001c0001t0002g0292 a0001c0010t0002g0320 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.3361-860T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975624 | |||||||
chr2:54975773 | T | C | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3361-1009A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975773 | |||||||
chr2:54975792 | T | G | 1 | a0002c0002t0003g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3361-1028A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975792 | |||||||
chr2:54975915 | T | A | 2 | a0001c0001t0001g0074 a0002c0002t0003g0031 |
2 | HG00544.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.3361-1151A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975915 | |||||||
chr2:54975947 | T | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1183A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975947 | |||||||
chr2:54975948 | A | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1184T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975948 | |||||||
chr2:54975949 | T | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1185A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54975949 | |||||||
chr2:54976071 | A | G | 9 | a0005c0005t0001g0323 a0005c0005t0001g0324 a0005c0005t0001g0325 others(6): Show |
9 | HG02109.hp1 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.3361-1307T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976071 | |||||||
chr2:54976192 | G | C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0237 others(5): Show |
8 | HG02080.hp1 NA18947.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.3361-1428C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976192 | |||||||
chr2:54976231 | T | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-1467A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976231 | |||||||
chr2:54976259 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-1495C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976259 | |||||||
chr2:54976316 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3361-1552G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976316 | |||||||
chr2:54976512 | G | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3361-1748C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976512 | |||||||
chr2:54976587 | G | A | 1 | a0004c0004t0002g0167 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.3361-1823C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976587 | |||||||
chr2:54976604 | A | C | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3361-1840T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976604 | |||||||
chr2:54976795 | C | G | 91 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(88): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.3361-2031G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976795 | |||||||
chr2:54976838 | C | G | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3361-2074G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976838 | |||||||
chr2:54976892 | A | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(88): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.3361-2128T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976892 | |||||||
chr2:54976907 | A | G | 4 | a0001c0001t0004g0193 a0001c0001t0004g0194 a0001c0001t0006g0309 others(1): Show |
4 | HG02109.hp2 HG02145.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-2143T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976907 | |||||||
chr2:54976947 | G | T | 1 | a0001c0001t0002g0189 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3361-2183C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54976947 | |||||||
chr2:54977017 | G | A | 1 | a0004c0004t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3361-2253C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977017 | |||||||
chr2:54977029 | C | T | 58 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(55): Show |
59 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3361-2265G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977029 | |||||||
chr2:54977083 | G | A | 4 | a0006c0006t0002g0003 a0006c0006t0002g0301 a0006c0006t0002g0302 others(1): Show |
6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3361-2319C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977083 | |||||||
chr2:54977127 | TA | T | 12 | a0001c0001t0005g0011 a0001c0001t0005g0281 a0001c0001t0005g0282 others(9): Show |
13 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.3361-2364delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977127 | |||||||
chr2:54977170 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3361-2406G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977170 | |||||||
chr2:54977362 | G | C | 182 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(179): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.3361-2598C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977362 | |||||||
chr2:54977374 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3361-2610G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977374 | |||||||
chr2:54977401 | A | G | 10 | a0001c0001t0001g0214 a0001c0001t0007g0332 a0001c0001t0007g0333 others(7): Show |
10 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3361-2637T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977401 | |||||||
chr2:54977406 | G | GT | 177 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(174): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3361-2643dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977406 | |||||||
chr2:54977406 | G | GTT | 20 | a0001c0001t0001g0087 a0001c0001t0001g0214 a0001c0001t0001g0273 others(17): Show |
20 | HG02132.hp2 HG02145.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.3361-2644_3361-264 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977406 | |||||||
chr2:54977439 | T | G | 1 | a0001c0001t0001g0314 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3361-2675A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977439 | |||||||
chr2:54977469 | C | T | 7 | a0001c0001t0002g0008 a0001c0001t0002g0141 a0001c0001t0002g0151 others(4): Show |
8 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(5): Show |
intron_variant | MODIFIER | c.3361-2705G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977469 | |||||||
chr2:54977631 | T | A | 1 | a0001c0001t0002g0133 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3361-2867A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977631 | |||||||
chr2:54977660 | A | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3361-2896T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977660 | |||||||
chr2:54977664 | C | G | 297 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(294): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.3361-2900G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977664 | |||||||
chr2:54977685 | G | A | 1 | a0001c0008t0008g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3361-2921C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977685 | |||||||
chr2:54977729 | T | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3361-2965A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977729 | |||||||
chr2:54977759 | G | T | 4 | a0001c0001t0002g0081 a0001c0001t0002g0133 a0001c0001t0002g0153 others(1): Show |
4 | NA18965.hp1 NA19056.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.3361-2995C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977759 | |||||||
chr2:54977895 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3361-3131C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977895 | |||||||
chr2:54977951 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-3187T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977951 | |||||||
chr2:54977956 | T | C | 297 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(294): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.3361-3192A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977956 | |||||||
chr2:54977988 | T | C | 181 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(178): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.3361-3224A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54977988 | |||||||
chr2:54978054 | T | G | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3361-3290A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978054 | |||||||
chr2:54978111 | A | C | 3 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 |
3 | HG03041.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3361-3347T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978111 | |||||||
chr2:54978126 | C | A | 297 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(294): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.3361-3362G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978126 | |||||||
chr2:54978187 | T | C | 9 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(6): Show |
9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3361-3423A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978187 | |||||||
chr2:54978335 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3361-3571G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978335 | |||||||
chr2:54978386 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0312 |
2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3361-3622C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978386 | |||||||
chr2:54978390 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0127 |
3 | HG02559.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3361-3626G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978390 | |||||||
chr2:54978393 | C | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3361-3629G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978393 | |||||||
chr2:54978405 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0001g0238 a0001c0001t0001g0239 others(1): Show |
4 | NA18947.hp2 NA18967.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.3361-3641A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978405 | |||||||
chr2:54978417 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3361-3653G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978417 | |||||||
chr2:54978431 | C | CA | 94 | a0001c0001t0001g0100 a0001c0001t0001g0124 a0001c0001t0001g0216 others(91): Show |
103 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.3361-3668dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | |||||||
chr2:54978431 | C | CAA | 15 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0142 others(12): Show |
15 | HG00323.hp1 HG00609.hp2 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.3361-3669_3361-366 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | |||||||
chr2:54978431 | CA | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(79): Show |
85 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.3361-3668delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | |||||||
chr2:54978431 | CAA | C | 10 | a0001c0001t0001g0214 a0001c0001t0007g0332 a0001c0001t0007g0333 others(7): Show |
10 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3361-3669_3361-366 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978431 | |||||||
chr2:54978811 | A | G | 249 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(246): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.3360+3704T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978811 | |||||||
chr2:54978869 | C | T | 9 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(6): Show |
9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+3646G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978869 | |||||||
chr2:54978923 | G | A | 13 | a0001c0001t0001g0214 a0001c0001t0001g0273 a0001c0001t0001g0275 others(10): Show |
13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+3592C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978923 | |||||||
chr2:54978938 | A | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3360+3577T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978938 | |||||||
chr2:54978998 | A | C | 1 | a0001c0001t0005g0296 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3360+3517T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54978998 | |||||||
chr2:54979011 | T | A | 2 | a0001c0001t0007g0332 a0001c0001t0007g0335 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3360+3504A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979011 | |||||||
chr2:54979052 | A | AT | 15 | a0001c0001t0001g0121 a0001c0001t0001g0253 a0001c0001t0002g0154 others(12): Show |
15 | HG02109.hp1 HG02572.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.3360+3462dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979052 | |||||||
chr2:54979052 | AT | A | 9 | a0001c0001t0002g0145 a0001c0001t0002g0189 a0001c0001t0002g0209 others(6): Show |
12 | HG00423.hp2 HG00738.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.3360+3462delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979052 | |||||||
chr2:54979170 | A | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3360+3345T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979170 | |||||||
chr2:54979193 | C | A | 1 | a0002c0002t0003g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3360+3322G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979193 | |||||||
chr2:54979208 | A | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0134 a0001c0001t0002g0141 others(8): Show |
12 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.3360+3307T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979208 | |||||||
chr2:54979227 | GT | G | 177 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(174): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.3360+3287delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979227 | |||||||
chr2:54979227 | GTT | G | 9 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(6): Show |
9 | HG02647.hp2 HG02723.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+3286_3360+328 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979227 | |||||||
chr2:54979393 | T | G | 1 | a0001c0001t0004g0139 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3360+3122A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979393 | |||||||
chr2:54979463 | G | A | 2 | a0001c0008t0017g0067 a0012c0020t0002g0315 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3360+3052C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979463 | |||||||
chr2:54979547 | T | C | 2 | a0004c0004t0002g0168 a0004c0004t0002g0191 |
2 | HG02523.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.3360+2968A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979547 | |||||||
chr2:54979642 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0023t0001g0322 others(1): Show |
4 | HG02040.hp2 HG02165.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3360+2873C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979642 | |||||||
chr2:54979927 | C | T | 15 | a0001c0001t0001g0214 a0001c0001t0001g0273 a0001c0001t0001g0275 others(12): Show |
15 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.3360+2588G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54979927 | |||||||
chr2:54980017 | A | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3360+2498T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980017 | |||||||
chr2:54980074 | T | A | 2 | a0005c0005t0001g0325 a0005c0005t0001g0327 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3360+2441A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980074 | |||||||
chr2:54980116 | T | C | 1 | a0004c0004t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3360+2399A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980116 | |||||||
chr2:54980266 | C | T | 1 | a0001c0001t0023g0150 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3360+2249G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980266 | |||||||
chr2:54980485 | A | T | 2 | a0001c0008t0017g0067 a0012c0020t0002g0315 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3360+2030T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980485 | |||||||
chr2:54980545 | T | A | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3360+1970A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980545 | |||||||
chr2:54980557 | C | T | 58 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(55): Show |
59 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3360+1958G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980557 | |||||||
chr2:54980583 | T | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3360+1932A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980583 | |||||||
chr2:54980759 | C | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(245): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.3360+1756G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980759 | |||||||
chr2:54980934 | T | C | 4 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0029 others(1): Show |
4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.3360+1581A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980934 | |||||||
chr2:54980992 | A | G | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3360+1523T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54980992 | |||||||
chr2:54981190 | G | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3360+1325C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981190 | |||||||
chr2:54981229 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3360+1286T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981229 | |||||||
chr2:54981276 | TG | T | 3 | a0001c0001t0002g0292 a0001c0010t0002g0320 a0001c0010t0002g0321 |
3 | HG01109.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3360+1238delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981276 | |||||||
chr2:54981277 | G | GT | 9 | a0001c0001t0002g0186 a0001c0001t0002g0189 a0001c0001t0002g0204 others(6): Show |
9 | HG01952.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.3360+1237dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981277 | |||||||
chr2:54981278 | T | G | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3360+1237A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981278 | |||||||
chr2:54981282 | TG | T | 13 | a0001c0001t0001g0214 a0001c0001t0001g0266 a0001c0001t0001g0276 others(10): Show |
13 | HG00099.hp2 HG00423.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3360+1232delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981282 | |||||||
chr2:54981283 | G | T | 191 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(188): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.3360+1232C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981283 | |||||||
chr2:54981283 | GT | G | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02896.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3360+1231delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981283 | |||||||
chr2:54981284 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3360+1231A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981284 | |||||||
chr2:54981295 | T | A | 1 | a0001c0001t0005g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3360+1220A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981295 | |||||||
chr2:54981296 | A | T | 3 | a0001c0001t0001g0216 a0014c0018t0019g0160 a0017c0016t0001g0107 |
3 | NA18906.hp1 NA18985.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.3360+1219T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981296 | |||||||
chr2:54981338 | A | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02735.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3360+1177T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981338 | |||||||
chr2:54981664 | G | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3360+851C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981664 | |||||||
chr2:54981732 | G | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(245): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.3360+783C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981732 | |||||||
chr2:54981733 | T | C | 13 | a0001c0001t0001g0214 a0001c0001t0001g0273 a0001c0001t0001g0275 others(10): Show |
13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+782A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981733 | |||||||
chr2:54981817 | A | ATATGAAT others(19): Show |
151 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(148): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.3360+697_3360+698i others(28): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981817 | |||||||
chr2:54981873 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3360+642G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981873 | |||||||
chr2:54981901 | GATTA | G | 3 | a0001c0001t0006g0303 a0001c0001t0006g0309 a0001c0001t0006g0310 |
3 | HG02145.hp2 HG02257.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3360+610_3360+613d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981901 | |||||||
chr2:54981947 | C | CTA | 13 | a0001c0001t0001g0214 a0001c0001t0001g0273 a0001c0001t0001g0275 others(10): Show |
13 | HG02145.hp1 HG02280.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.3360+566_3360+567d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54981947 | |||||||
chr2:54982041 | G | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(83): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.3360+474C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982041 | |||||||
chr2:54982048 | G | A | 1 | a0002c0002t0003g0021 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3360+467C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982048 | |||||||
chr2:54982090 | G | A | 28 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0139 others(25): Show |
30 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.3360+425C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982090 | |||||||
chr2:54982099 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3360+416C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982099 | |||||||
chr2:54982143 | ACGGGGTT others(1): Show |
A | 30 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(27): Show |
31 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.3360+364_3360+371d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982143 | |||||||
chr2:54982252 | G | A | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3360+263C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 5/8 | chr2 | 54982252 | |||||||
chr2:54982850 | A | G | 2 | a0001c0001t0004g0198 a0001c0001t0004g0218 |
2 | HG02717.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3222-197T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982850 | |||||||
chr2:54982888 | A | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-235T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982888 | |||||||
chr2:54982970 | T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3222-317A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982970 | |||||||
chr2:54982979 | G | T | 1 | a0002c0002t0003g0039 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3222-326C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54982979 | |||||||
chr2:54983065 | G | GT | 6 | a0001c0001t0002g0204 a0001c0001t0005g0277 a0002c0002t0003g0027 others(3): Show |
6 | NA18952.hp1 NA18960.hp2 NA19001.hp2 others(3): Show |
intron_variant | MODIFIER | c.3222-413dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983065 | |||||||
chr2:54983135 | T | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-482A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983135 | |||||||
chr2:54983207 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3222-554C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983207 | |||||||
chr2:54983280 | C | T | 4 | a0005c0005t0001g0324 a0005c0005t0001g0326 a0005c0005t0001g0328 others(1): Show |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.3222-627G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983280 | |||||||
chr2:54983321 | T | TAATA | 77 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0134 others(74): Show |
78 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.3222-672_3222-669d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | |||||||
chr2:54983321 | T | TAATAAAT others(1): Show |
9 | a0001c0001t0005g0296 a0001c0001t0005g0299 a0001c0001t0005g0300 others(6): Show |
9 | HG01168.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3222-676_3222-669d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | |||||||
chr2:54983321 | T | TAATAAAT others(5): Show |
5 | a0001c0001t0003g0129 a0001c0001t0005g0294 a0001c0001t0005g0297 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3222-680_3222-669d others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | |||||||
chr2:54983321 | TAATA | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3222-672_3222-669d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | |||||||
chr2:54983321 | TAATAAAT others(1): Show |
T | 8 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(5): Show |
8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3222-676_3222-669d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983321 | |||||||
chr2:54983352 | T | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(32): Show |
36 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.3222-699A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983352 | |||||||
chr2:54983368 | G | A | 1 | a0016c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3222-715C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983368 | |||||||
chr2:54983469 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(79): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3222-816A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983469 | |||||||
chr2:54983518 | A | C | 1 | a0001c0001t0005g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3222-865T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983518 | |||||||
chr2:54983582 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3222-929G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983582 | |||||||
chr2:54983617 | T | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-964A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983617 | |||||||
chr2:54983658 | G | A | 2 | a0001c0001t0011g0268 a0012c0020t0002g0315 |
2 | HG03516.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3222-1005C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983658 | |||||||
chr2:54983720 | C | T | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3222-1067G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983720 | |||||||
chr2:54983721 | G | A | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3222-1068C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54983721 | |||||||
chr2:54984010 | T | G | 8 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(5): Show |
8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.3222-1357A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984010 | |||||||
chr2:54984036 | C | A | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3222-1383G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984036 | |||||||
chr2:54984160 | C | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3222-1507G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984160 | |||||||
chr2:54984179 | C | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3222-1526G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984179 | |||||||
chr2:54984188 | C | A | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3222-1535G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984188 | |||||||
chr2:54984310 | G | A | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3222-1657C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984310 | |||||||
chr2:54984394 | A | T | 1 | a0001c0001t0009g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3222-1741T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984394 | |||||||
chr2:54984397 | T | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3222-1744A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984397 | |||||||
chr2:54984501 | G | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3222-1848C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984501 | |||||||
chr2:54984709 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3222-2056A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984709 | |||||||
chr2:54984748 | C | G | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3222-2095G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984748 | |||||||
chr2:54984806 | A | G | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-2153T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984806 | |||||||
chr2:54984807 | G | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3222-2154C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984807 | |||||||
chr2:54984884 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3222-2231A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54984884 | |||||||
chr2:54985043 | G | T | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3222-2390C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985043 | |||||||
chr2:54985048 | A | G | 2 | a0002c0002t0002g0047 a0002c0002t0002g0060 |
2 | NA18978.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.3222-2395T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985048 | |||||||
chr2:54985153 | C | CT | 58 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(55): Show |
59 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.3221+2337dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | C | CTT | 65 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(62): Show |
65 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3221+2336_3221+233 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | C | CTTT | 23 | a0001c0001t0001g0078 a0001c0001t0001g0093 a0001c0001t0001g0100 others(20): Show |
23 | HG01175.hp2 HG01361.hp1 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.3221+2335_3221+233 others(7): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | C | CTTTT | 11 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0095 others(8): Show |
11 | HG00099.hp1 HG01256.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.3221+2334_3221+233 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | C | CTTTTTTT others(6): Show |
1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3221+2325_3221+233 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | CT | C | 77 | a0001c0001t0001g0214 a0001c0001t0001g0251 a0001c0001t0002g0001 others(74): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.3221+2337delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | CTT | C | 30 | a0001c0001t0002g0136 a0001c0001t0005g0277 a0001c0001t0005g0278 others(27): Show |
30 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.3221+2336_3221+233 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0003g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3221+2325_3221+233 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985153 | CTTTTTTT others(9): Show |
C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
7 | NA18951.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+2322_3221+233 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985153 | |||||||
chr2:54985191 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3221+2300C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985191 | |||||||
chr2:54985201 | T | C | 239 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(236): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3221+2290A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985201 | |||||||
chr2:54985202 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3221+2289A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985202 | |||||||
chr2:54985288 | T | C | 1 | a0001c0001t0004g0201 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3221+2203A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985288 | |||||||
chr2:54985339 | T | G | 2 | a0001c0001t0005g0296 a0001c0001t0005g0297 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3221+2152A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985339 | |||||||
chr2:54985359 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(78): Show |
82 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.3221+2132A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985359 | |||||||
chr2:54985437 | G | C | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+2054C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985437 | |||||||
chr2:54985454 | T | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3221+2037A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985454 | |||||||
chr2:54985769 | A | C | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1722T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985769 | |||||||
chr2:54985787 | G | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1704C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985787 | |||||||
chr2:54985789 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(119): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3221+1702A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54985789 | |||||||
chr2:54986174 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3221+1317T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986174 | |||||||
chr2:54986184 | G | A | 30 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(27): Show |
32 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(29): Show |
intron_variant | MODIFIER | c.3221+1307C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986184 | |||||||
chr2:54986262 | G | A | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1229C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986262 | |||||||
chr2:54986263 | A | G | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+1228T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986263 | |||||||
chr2:54986297 | T | C | 1 | a0002c0002t0001g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3221+1194A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986297 | |||||||
chr2:54986727 | C | T | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3221+764G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986727 | |||||||
chr2:54986728 | G | A | 3 | a0001c0001t0002g0135 a0001c0001t0002g0162 a0001c0001t0002g0163 |
3 | HG01074.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3221+763C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986728 | |||||||
chr2:54986733 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3221+758A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986733 | |||||||
chr2:54986776 | C | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3221+715G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986776 | |||||||
chr2:54986785 | T | C | 7 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0011g0264 others(4): Show |
7 | HG02040.hp2 HG02132.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3221+706A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986785 | |||||||
chr2:54986854 | C | CAATTAAA others(7): Show |
1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3221+623_3221+636d others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986854 | |||||||
chr2:54986863 | A | G | 2 | a0001c0008t0017g0067 a0012c0020t0002g0315 |
2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3221+628T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986863 | |||||||
chr2:54986879 | C | T | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3221+612G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986879 | |||||||
chr2:54986929 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3221+562A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54986929 | |||||||
chr2:54987309 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3221+182G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54987309 | |||||||
chr2:54987482 | A | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(181): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.3221+9T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 4/8 | chr2 | 54987482 | |||||||
chr2:54987776 | C | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3014-78G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987776 | |||||||
chr2:54987842 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3014-144A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987842 | |||||||
chr2:54987878 | T | A | 1 | a0001c0001t0002g0188 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3014-180A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987878 | |||||||
chr2:54987967 | G | A | 1 | a0001c0001t0005g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3014-269C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987967 | |||||||
chr2:54987999 | A | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3014-301T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54987999 | |||||||
chr2:54988332 | G | T | 1 | a0001c0001t0005g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3014-634C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988332 | |||||||
chr2:54988347 | A | C | 6 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(3): Show |
6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3014-649T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988347 | |||||||
chr2:54988481 | G | A | 29 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(26): Show |
31 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.3014-783C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988481 | |||||||
chr2:54988502 | T | C | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-804A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988502 | |||||||
chr2:54988689 | G | A | 246 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(243): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.3014-991C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988689 | |||||||
chr2:54988954 | C | T | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-1256G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988954 | |||||||
chr2:54988982 | T | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-1284A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988982 | |||||||
chr2:54988991 | T | C | 32 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(29): Show |
34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3014-1293A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54988991 | |||||||
chr2:54989084 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3014-1386A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989084 | |||||||
chr2:54989085 | G | A | 8 | a0001c0001t0001g0214 a0001c0001t0007g0332 a0001c0001t0007g0333 others(5): Show |
8 | HG02280.hp1 HG02647.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3014-1387C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989085 | |||||||
chr2:54989337 | C | T | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3014-1639G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989337 | |||||||
chr2:54989372 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-1674G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989372 | |||||||
chr2:54989409 | C | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(84): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3014-1711G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989409 | |||||||
chr2:54989417 | G | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-1719C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989417 | |||||||
chr2:54989517 | G | A | 2 | a0001c0001t0014g0146 a0001c0001t0014g0254 |
2 | HG03654.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3014-1819C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989517 | |||||||
chr2:54989771 | G | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3014-2073C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989771 | |||||||
chr2:54989857 | A | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-2159T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989857 | |||||||
chr2:54989998 | C | T | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-2300G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54989998 | |||||||
chr2:54990182 | T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-2484A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990182 | |||||||
chr2:54990294 | A | T | 32 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(29): Show |
34 | HG01109.hp1 HG01167.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.3014-2596T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990294 | |||||||
chr2:54990310 | C | CG | 3 | a0001c0001t0001g0112 a0001c0001t0001g0276 a0014c0018t0019g0160 |
3 | HG02145.hp1 NA18956.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3014-2613dupC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990310 | |||||||
chr2:54990324 | G | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-2626C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990324 | |||||||
chr2:54990382 | T | C | 51 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0003g0128 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-2684A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990382 | |||||||
chr2:54990443 | G | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-2745C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990443 | |||||||
chr2:54990468 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-2770A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990468 | |||||||
chr2:54990478 | TTAA | T | 3 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 |
3 | HG02818.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3014-2783_3014-278 others(7): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990478 | |||||||
chr2:54990651 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-2953A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990651 | |||||||
chr2:54990681 | T | C | 1 | a0011c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3014-2983A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990681 | |||||||
chr2:54990721 | T | A | 1 | a0009c0022t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3014-3023A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990721 | |||||||
chr2:54990722 | A | T | 1 | a0009c0022t0001g0319 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3014-3024T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990722 | |||||||
chr2:54990787 | T | A | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3014-3089A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990787 | |||||||
chr2:54990816 | C | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-3118G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990816 | |||||||
chr2:54990835 | G | A | 51 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0003g0128 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-3137C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990835 | |||||||
chr2:54990871 | C | T | 2 | a0001c0001t0009g0164 a0001c0001t0009g0316 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3014-3173G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990871 | |||||||
chr2:54990890 | A | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(83): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.3014-3192T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990890 | |||||||
chr2:54990990 | G | A | 1 | a0004c0004t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3014-3292C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54990990 | |||||||
chr2:54991382 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-3684A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991382 | |||||||
chr2:54991622 | C | T | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3014-3924G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991622 | |||||||
chr2:54991655 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(79): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3014-3957C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991655 | |||||||
chr2:54991669 | G | T | 88 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(85): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.3014-3971C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991669 | |||||||
chr2:54991722 | G | C | 1 | a0002c0002t0018g0023 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3014-4024C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991722 | |||||||
chr2:54991864 | A | T | 2 | a0003c0003t0013g0071 a0003c0003t0013g0072 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3014-4166T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991864 | |||||||
chr2:54991969 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-4271G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991969 | |||||||
chr2:54991999 | C | T | 31 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(28): Show |
32 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.3014-4301G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54991999 | |||||||
chr2:54992199 | A | C | 1 | a0001c0001t0002g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3014-4501T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992199 | |||||||
chr2:54992380 | G | T | 34 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(31): Show |
35 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.3014-4682C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992380 | |||||||
chr2:54992493 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3014-4795T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992493 | |||||||
chr2:54992523 | C | T | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3014-4825G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992523 | |||||||
chr2:54992663 | G | A | 34 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(31): Show |
35 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.3014-4965C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992663 | |||||||
chr2:54992674 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3014-4976T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992674 | |||||||
chr2:54992760 | A | C | 1 | a0001c0001t0020g0118 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3014-5062T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992760 | |||||||
chr2:54992853 | A | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(83): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.3014-5155T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992853 | |||||||
chr2:54992885 | C | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(83): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.3014-5187G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992885 | |||||||
chr2:54992896 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-5198G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54992896 | |||||||
chr2:54993028 | T | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-5330A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993028 | |||||||
chr2:54993061 | G | A | 150 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(147): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.3014-5363C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993061 | |||||||
chr2:54993073 | CG | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.3014-5376delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993073 | |||||||
chr2:54993074 | G | GA | 29 | a0001c0001t0004g0193 a0001c0001t0005g0011 a0001c0001t0005g0278 others(26): Show |
30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.3014-5377_3014-537 others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | |||||||
chr2:54993074 | G | GAA | 3 | a0001c0001t0004g0194 a0001c0001t0005g0293 a0001c0001t0005g0298 |
3 | HG02109.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3014-5377_3014-537 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | |||||||
chr2:54993074 | GGA | G | 32 | a0001c0001t0001g0114 a0001c0001t0001g0214 a0001c0001t0001g0273 others(29): Show |
34 | HG01109.hp1 HG01346.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.3014-5378_3014-537 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993074 | |||||||
chr2:54993075 | G | A | 37 | a0001c0001t0001g0119 a0001c0001t0004g0193 a0001c0001t0004g0194 others(34): Show |
38 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.3014-5377C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | |||||||
chr2:54993075 | G | GA | 6 | a0001c0001t0001g0240 a0001c0001t0002g0188 a0001c0001t0002g0311 others(3): Show |
6 | HG01175.hp2 HG01361.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-5378dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | |||||||
chr2:54993075 | GA | G | 12 | a0001c0001t0001g0236 a0001c0001t0002g0132 a0001c0008t0017g0067 others(9): Show |
12 | HG00323.hp1 HG02109.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.3014-5378delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993075 | |||||||
chr2:54993076 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3014-5378T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993076 | |||||||
chr2:54993099 | G | C | 1 | a0001c0001t0011g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3014-5401C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993099 | |||||||
chr2:54993122 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3014-5424C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993122 | |||||||
chr2:54993170 | A | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-5472T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993170 | |||||||
chr2:54993224 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3014-5526A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993224 | |||||||
chr2:54993381 | T | A | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3014-5683A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993381 | |||||||
chr2:54993439 | G | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3014-5741C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993439 | |||||||
chr2:54993448 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3014-5750G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993448 | |||||||
chr2:54993671 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3014-5973A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993671 | |||||||
chr2:54993824 | T | C | 173 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(170): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.3014-6126A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54993824 | |||||||
chr2:54994013 | A | G | 1 | a0001c0001t0004g0194 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3014-6315T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994013 | |||||||
chr2:54994147 | T | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-6449A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994147 | |||||||
chr2:54994371 | A | G | 1 | a0001c0008t0008g0261 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3014-6673T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994371 | |||||||
chr2:54994410 | C | T | 26 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(23): Show |
28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3014-6712G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994410 | |||||||
chr2:54994591 | A | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-6893T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994591 | |||||||
chr2:54994611 | G | C | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-6913C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994611 | |||||||
chr2:54994699 | G | T | 39 | a0001c0001t0004g0138 a0001c0001t0004g0197 a0001c0001t0004g0202 others(36): Show |
40 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3014-7001C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994699 | |||||||
chr2:54994861 | A | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-7163T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994861 | |||||||
chr2:54994944 | T | C | 2 | a0001c0001t0007g0332 a0001c0001t0007g0335 |
2 | HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3014-7246A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994944 | |||||||
chr2:54994966 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3014-7268G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994966 | |||||||
chr2:54994970 | C | T | 153 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(150): Show |
157 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.3014-7272G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994970 | |||||||
chr2:54994996 | G | A | 87 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(84): Show |
96 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.3014-7298C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54994996 | |||||||
chr2:54995029 | G | C | 1 | a0001c0001t0004g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3014-7331C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995029 | |||||||
chr2:54995082 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3014-7384T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995082 | |||||||
chr2:54995109 | C | A | 2 | a0001c0001t0005g0293 a0001c0001t0005g0298 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3014-7411G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995109 | |||||||
chr2:54995202 | T | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3014-7504A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995202 | |||||||
chr2:54995256 | T | A | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3014-7558A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995256 | |||||||
chr2:54995289 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3014-7591T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995289 | |||||||
chr2:54995494 | A | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(77): Show |
81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3014-7796T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995494 | |||||||
chr2:54995544 | G | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(77): Show |
81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3014-7846C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995544 | |||||||
chr2:54995569 | A | G | 1 | a0004c0004t0002g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3014-7871T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995569 | |||||||
chr2:54995688 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3014-7990G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995688 | |||||||
chr2:54995881 | T | G | 1 | a0007c0007t0012g0065 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3014-8183A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995881 | |||||||
chr2:54995971 | T | A | 51 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0003g0128 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-8273A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995971 | |||||||
chr2:54995988 | G | C | 1 | a0001c0001t0011g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3014-8290C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54995988 | |||||||
chr2:54996009 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3014-8311C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996009 | |||||||
chr2:54996043 | T | C | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3014-8345A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996043 | |||||||
chr2:54996146 | C | T | 147 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(144): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.3014-8448G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996146 | |||||||
chr2:54996223 | A | G | 1 | a0002c0002t0003g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3014-8525T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996223 | |||||||
chr2:54996286 | C | T | 10 | a0001c0001t0024g0080 a0005c0005t0001g0323 a0005c0005t0001g0324 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.3014-8588G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996286 | |||||||
chr2:54996319 | G | A | 24 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(21): Show |
26 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.3014-8621C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996319 | |||||||
chr2:54996502 | G | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(53): Show |
57 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.3014-8804C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996502 | |||||||
chr2:54996550 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3014-8852C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996550 | |||||||
chr2:54996698 | C | T | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-9000G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54996698 | |||||||
chr2:54997037 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3014-9339G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997037 | |||||||
chr2:54997273 | C | T | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9575G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997273 | |||||||
chr2:54997278 | T | C | 1 | a0001c0001t0002g0153 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3014-9580A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997278 | |||||||
chr2:54997321 | C | T | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9623G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997321 | |||||||
chr2:54997357 | A | G | 1 | a0011c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3014-9659T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997357 | |||||||
chr2:54997357 | A | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3014-9659T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997357 | |||||||
chr2:54997522 | T | C | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9824A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997522 | |||||||
chr2:54997532 | A | C | 19 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(16): Show |
19 | HG02080.hp1 NA18942.hp2 NA18947.hp2 others(16): Show |
intron_variant | MODIFIER | c.3014-9834T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997532 | |||||||
chr2:54997567 | T | C | 11 | a0001c0001t0001g0214 a0001c0001t0007g0332 a0001c0001t0007g0333 others(8): Show |
11 | HG02109.hp1 HG02280.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3014-9869A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997567 | |||||||
chr2:54997574 | T | C | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-9876A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997574 | |||||||
chr2:54997775 | T | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-10077A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54997775 | |||||||
chr2:54998061 | G | A | 1 | a0002c0002t0003g0042 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3014-10363C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998061 | |||||||
chr2:54998064 | A | C | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3014-10366T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998064 | |||||||
chr2:54998167 | T | C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(73): Show |
77 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3014-10469A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998167 | |||||||
chr2:54998246 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-10548C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998246 | |||||||
chr2:54998330 | TA | T | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0012g0064 others(2): Show |
5 | HG01167.hp1 HG02559.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3014-10633delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998330 | |||||||
chr2:54998494 | T | C | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-10796A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998494 | |||||||
chr2:54998666 | T | C | 1 | a0001c0001t0002g0175 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3014-10968A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998666 | |||||||
chr2:54998683 | C | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3014-10985G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998683 | |||||||
chr2:54998701 | G | A | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-11003C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998701 | |||||||
chr2:54998809 | T | C | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-11111A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998809 | |||||||
chr2:54998873 | G | A | 218 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(215): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.3014-11175C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54998873 | |||||||
chr2:54999403 | T | C | 3 | a0005c0005t0001g0323 a0005c0005t0001g0325 a0005c0005t0001g0327 |
3 | HG02109.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3014-11705A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999403 | |||||||
chr2:54999792 | C | T | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3014-12094G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999792 | |||||||
chr2:54999809 | G | A | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-12111C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999809 | |||||||
chr2:54999891 | T | C | 10 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(7): Show |
10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3014-12193A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 54999891 | |||||||
chr2:55000054 | T | C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0182 |
2 | HG02165.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.3014-12356A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000054 | |||||||
chr2:55000095 | C | G | 144 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(141): Show |
148 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.3014-12397G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000095 | |||||||
chr2:55000113 | A | G | 1 | a0001c0001t0014g0254 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3014-12415T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000113 | |||||||
chr2:55000210 | G | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.3014-12512C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000210 | |||||||
chr2:55000239 | C | G | 247 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.3014-12541G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000239 | |||||||
chr2:55000247 | G | T | 117 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(114): Show |
119 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.3014-12549C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000247 | |||||||
chr2:55000322 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3014-12624G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000322 | |||||||
chr2:55000346 | T | TA | 7 | a0001c0001t0004g0079 a0001c0001t0004g0193 a0001c0001t0004g0194 others(4): Show |
7 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3014-12649dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000346 | |||||||
chr2:55000835 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3014-13137C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000835 | |||||||
chr2:55000987 | A | AT | 28 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(25): Show |
29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-13290dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55000987 | |||||||
chr2:55001034 | A | C | 6 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(3): Show |
6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3014-13336T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001034 | |||||||
chr2:55001256 | C | T | 239 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-13558G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001256 | |||||||
chr2:55001363 | C | T | 239 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-13665G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001363 | |||||||
chr2:55001429 | T | A | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3014-13731A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001429 | |||||||
chr2:55001437 | T | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0312 |
2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.3014-13739A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001437 | |||||||
chr2:55001504 | A | G | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-13806T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001504 | |||||||
chr2:55001585 | T | C | 26 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(23): Show |
28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3014-13887A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001585 | |||||||
chr2:55001587 | G | C | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(86): Show |
90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3014-13889C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001587 | |||||||
chr2:55001699 | T | C | 102 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0214 others(99): Show |
103 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.3014-14001A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001699 | |||||||
chr2:55001725 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.3014-14027C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001725 | |||||||
chr2:55001811 | A | G | 51 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.3014-14113T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001811 | |||||||
chr2:55001947 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3014-14249G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001947 | |||||||
chr2:55001949 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3014-14251C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001949 | |||||||
chr2:55001968 | T | C | 1 | a0001c0001t0024g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3014-14270A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001968 | |||||||
chr2:55001990 | T | A | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14292A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001990 | |||||||
chr2:55001991 | A | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14293T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55001991 | |||||||
chr2:55002049 | T | TTTTA | 92 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(89): Show |
93 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.3014-14355_3014-14 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002049 | |||||||
chr2:55002057 | A | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-14359T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002057 | |||||||
chr2:55002058 | T | C | 6 | a0001c0008t0017g0067 a0007c0007t0004g0062 a0007c0007t0004g0063 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-14360A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002058 | |||||||
chr2:55002173 | C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-14475G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002173 | |||||||
chr2:55002203 | C | T | 28 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(25): Show |
29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-14505G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002203 | |||||||
chr2:55002207 | C | T | 28 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(25): Show |
29 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3014-14509G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002207 | |||||||
chr2:55002231 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3014-14533A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002231 | |||||||
chr2:55002237 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3014-14539A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002237 | |||||||
chr2:55002351 | G | T | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3014-14653C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002351 | |||||||
chr2:55002364 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-14666A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002364 | |||||||
chr2:55002372 | T | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(190): Show |
195 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.3014-14674A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002372 | |||||||
chr2:55002383 | A | G | 1 | a0001c0001t0024g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3014-14685T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002383 | |||||||
chr2:55002691 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3014-14993G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002691 | |||||||
chr2:55002719 | C | A | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3014-15021G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002719 | |||||||
chr2:55002806 | T | C | 3 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0002c0002t0018g0023 |
3 | HG03491.hp2 NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3014-15108A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002806 | |||||||
chr2:55002820 | C | A | 4 | a0001c0001t0001g0241 a0001c0001t0001g0247 a0001c0001t0001g0257 others(1): Show |
4 | NA18969.hp2 NA18991.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.3014-15122G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002820 | |||||||
chr2:55002884 | T | C | 11 | a0001c0001t0002g0147 a0001c0001t0002g0155 a0001c0001t0002g0190 others(8): Show |
12 | HG01070.hp2 HG01071.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.3014-15186A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002884 | |||||||
chr2:55002933 | T | A | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-15235A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002933 | |||||||
chr2:55002949 | C | T | 88 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(85): Show |
89 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.3014-15251G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002949 | |||||||
chr2:55002951 | A | T | 88 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(85): Show |
89 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.3014-15253T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55002951 | |||||||
chr2:55003047 | T | C | 4 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(1): Show |
4 | HG02145.hp1 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.3014-15349A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003047 | |||||||
chr2:55003083 | C | T | 239 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(236): Show |
244 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.3014-15385G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003083 | |||||||
chr2:55003278 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-15580A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003278 | |||||||
chr2:55003410 | C | T | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3014-15712G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003410 | |||||||
chr2:55003906 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3014-16208A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003906 | |||||||
chr2:55003918 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3014-16220G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003918 | |||||||
chr2:55003982 | T | A | 7 | a0001c0008t0017g0067 a0007c0007t0004g0062 a0007c0007t0004g0063 others(4): Show |
7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3014-16284A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003982 | |||||||
chr2:55003991 | A | C | 7 | a0001c0008t0017g0067 a0007c0007t0004g0062 a0007c0007t0004g0063 others(4): Show |
7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.3014-16293T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003991 | |||||||
chr2:55003997 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3014-16299C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55003997 | |||||||
chr2:55004160 | T | G | 2 | a0001c0001t0002g0189 a0001c0001t0002g0311 |
2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3014-16462A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004160 | |||||||
chr2:55004220 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3014-16522G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004220 | |||||||
chr2:55004293 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3014-16595C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004293 | |||||||
chr2:55004312 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3014-16614A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004312 | |||||||
chr2:55004379 | G | A | 85 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(82): Show |
86 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.3014-16681C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004379 | |||||||
chr2:55004427 | G | A | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-16729C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004427 | |||||||
chr2:55004521 | T | A | 10 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(7): Show |
10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3014-16823A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004521 | |||||||
chr2:55004562 | G | A | 1 | a0001c0001t0005g0299 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3014-16864C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004562 | |||||||
chr2:55004602 | G | C | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3014-16904C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004602 | |||||||
chr2:55004672 | G | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-16974C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004672 | |||||||
chr2:55004693 | C | T | 38 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(35): Show |
39 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.3014-16995G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004693 | |||||||
chr2:55004705 | G | A | 58 | a0001c0001t0001g0214 a0001c0001t0004g0077 a0001c0001t0004g0079 others(55): Show |
61 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.3014-17007C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004705 | |||||||
chr2:55004792 | T | C | 93 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(90): Show |
94 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.3014-17094A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004792 | |||||||
chr2:55004806 | T | C | 5 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(2): Show |
5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.3014-17108A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004806 | |||||||
chr2:55004848 | C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17150G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004848 | |||||||
chr2:55004859 | G | C | 14 | a0002c0002t0001g0056 a0002c0002t0003g0014 a0002c0002t0003g0024 others(11): Show |
14 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.3014-17161C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55004859 | |||||||
chr2:55005117 | G | C | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17419C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005117 | |||||||
chr2:55005118 | C | T | 1 | a0001c0023t0001g0322 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3014-17420G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005118 | |||||||
chr2:55005220 | C | T | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-17522G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005220 | |||||||
chr2:55005561 | G | A | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014-17863C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005561 | |||||||
chr2:55005649 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3014-17951A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005649 | |||||||
chr2:55005814 | G | C | 6 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(3): Show |
6 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014-18116C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005814 | |||||||
chr2:55005859 | A | G | 1 | a0001c0001t0005g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3014-18161T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005859 | |||||||
chr2:55005973 | A | T | 1 | a0001c0001t0011g0267 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3014-18275T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55005973 | |||||||
chr2:55006053 | C | T | 2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3014-18355G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006053 | |||||||
chr2:55006054 | G | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(32): Show |
36 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.3014-18356C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006054 | |||||||
chr2:55006197 | T | G | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3014-18499A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006197 | |||||||
chr2:55006222 | A | C | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3014-18524T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006222 | |||||||
chr2:55006392 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3013+18694G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006392 | |||||||
chr2:55006412 | G | A | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.3013+18674C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006412 | |||||||
chr2:55006688 | A | G | 1 | a0007c0007t0004g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3013+18398T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006688 | |||||||
chr2:55006806 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3013+18280G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006806 | |||||||
chr2:55006806 | C | G | 3 | a0001c0001t0011g0264 a0001c0001t0011g0267 a0001c0001t0011g0268 |
3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+18280G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55006806 | |||||||
chr2:55007126 | C | A | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+17960G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007126 | |||||||
chr2:55007145 | T | C | 2 | a0001c0001t0001g0272 a0001c0017t0001g0265 |
2 | HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.3013+17941A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007145 | |||||||
chr2:55007168 | C | T | 1 | a0014c0018t0019g0160 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3013+17918G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007168 | |||||||
chr2:55007176 | T | C | 27 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(24): Show |
29 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.3013+17910A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007176 | |||||||
chr2:55007182 | G | T | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+17904C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007182 | |||||||
chr2:55007209 | C | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0098 others(2): Show |
5 | HG01081.hp2 HG01257.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+17877G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007209 | |||||||
chr2:55007335 | C | A | 17 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(14): Show |
17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.3013+17751G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007335 | |||||||
chr2:55007453 | T | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3013+17633A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007453 | |||||||
chr2:55007794 | A | G | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+17292T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55007794 | |||||||
chr2:55008110 | G | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+16976C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008110 | |||||||
chr2:55008142 | A | AAC | 55 | a0001c0001t0001g0078 a0001c0001t0001g0086 a0001c0001t0001g0087 others(52): Show |
55 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.3013+16942_3013+16 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACAC | 16 | a0001c0001t0001g0083 a0001c0001t0001g0093 a0001c0001t0001g0096 others(13): Show |
17 | HG00423.hp1 HG01167.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.3013+16940_3013+16 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACAC | 41 | a0001c0001t0001g0110 a0001c0001t0001g0126 a0001c0001t0001g0223 others(38): Show |
41 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(38): Show |
intron_variant | MODIFIER | c.3013+16938_3013+16 others(12): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACACA others(1): Show |
43 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0075 others(40): Show |
45 | HG00323.hp2 HG00544.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.3013+16936_3013+16 others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACACA others(3): Show |
48 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0113 others(45): Show |
49 | HG00558.hp2 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.3013+16934_3013+16 others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACACA others(5): Show |
14 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0275 others(11): Show |
15 | HG00642.hp1 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3013+16932_3013+16 others(18): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACACA others(7): Show |
3 | a0001c0001t0007g0335 a0001c0008t0017g0067 a0002c0011t0003g0046 |
3 | HG01943.hp2 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3013+16930_3013+16 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | AACACACA others(9): Show |
1 | a0002c0002t0003g0044 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3013+16928_3013+16 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | ACACAC | 3 | a0001c0001t0001g0270 a0001c0001t0002g0070 a0001c0001t0004g0079 |
3 | HG02165.hp2 HG02615.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.3013+16943_3013+16 others(11): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008142 | A | ACACACAC others(4): Show |
2 | a0002c0002t0003g0020 a0003c0003t0013g0072 |
2 | HG00544.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3013+16943_3013+16 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008142 | |||||||
chr2:55008237 | T | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+16849A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008237 | |||||||
chr2:55008367 | G | C | 3 | a0001c0001t0002g0292 a0001c0010t0002g0320 a0001c0010t0002g0321 |
3 | HG01109.hp2 HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3013+16719C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008367 | |||||||
chr2:55008731 | T | C | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+16355A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008731 | |||||||
chr2:55008748 | CTTAAG | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+16333_3013+16 others(11): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008748 | |||||||
chr2:55008830 | T | C | 33 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(30): Show |
36 | HG00099.hp2 HG00738.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.3013+16256A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008830 | |||||||
chr2:55008954 | A | G | 4 | a0006c0006t0002g0003 a0006c0006t0002g0301 a0006c0006t0002g0302 others(1): Show |
6 | HG00738.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+16132T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55008954 | |||||||
chr2:55009039 | A | AT | 97 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(94): Show |
98 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.3013+16046dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009039 | |||||||
chr2:55009224 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(69): Show |
73 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.3013+15862G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009224 | |||||||
chr2:55009312 | T | C | 96 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(93): Show |
97 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.3013+15774A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009312 | |||||||
chr2:55009438 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3013+15648C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009438 | |||||||
chr2:55009490 | T | G | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3013+15596A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009490 | |||||||
chr2:55009526 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+15560C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009526 | |||||||
chr2:55009732 | G | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+15354C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009732 | |||||||
chr2:55009863 | GAC | G | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15221_3013+15 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009863 | |||||||
chr2:55009866 | T | G | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15220A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009866 | |||||||
chr2:55009868 | A | T | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15218T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009868 | |||||||
chr2:55009869 | A | T | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15217T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009869 | |||||||
chr2:55009870 | A | T | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15216T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009870 | |||||||
chr2:55009873 | A | G | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+15213T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009873 | |||||||
chr2:55009880 | C | T | 1 | a0002c0002t0003g0050 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3013+15206G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009880 | |||||||
chr2:55009913 | T | G | 97 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(94): Show |
98 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.3013+15173A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55009913 | |||||||
chr2:55010131 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3013+14955C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010131 | |||||||
chr2:55010161 | T | C | 1 | a0001c0001t0005g0285 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3013+14925A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010161 | |||||||
chr2:55010577 | A | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3013+14509T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010577 | |||||||
chr2:55010770 | A | C | 6 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(3): Show |
6 | HG02647.hp2 HG02970.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+14316T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55010770 | |||||||
chr2:55011096 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3013+13990T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011096 | |||||||
chr2:55011202 | C | A | 1 | a0001c0001t0002g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3013+13884G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011202 | |||||||
chr2:55011293 | C | T | 67 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(64): Show |
68 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.3013+13793G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011293 | |||||||
chr2:55011371 | T | A | 1 | a0002c0002t0003g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3013+13715A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011371 | |||||||
chr2:55011404 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3013+13682A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011404 | |||||||
chr2:55011452 | C | G | 1 | a0001c0008t0008g0259 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3013+13634G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011452 | |||||||
chr2:55011458 | C | T | 2 | a0003c0003t0004g0317 a0003c0003t0004g0318 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3013+13628G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011458 | |||||||
chr2:55011521 | G | A | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+13565C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011521 | |||||||
chr2:55011540 | C | T | 3 | a0001c0001t0011g0264 a0001c0001t0011g0267 a0001c0001t0011g0268 |
3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+13546G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011540 | |||||||
chr2:55011541 | G | A | 56 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(53): Show |
57 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.3013+13545C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011541 | |||||||
chr2:55011620 | C | G | 82 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(79): Show |
85 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.3013+13466G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011620 | |||||||
chr2:55011715 | C | G | 163 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(160): Show |
165 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.3013+13371G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011715 | |||||||
chr2:55011723 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3013+13363A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011723 | |||||||
chr2:55011748 | G | A | 1 | a0001c0001t0003g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3013+13338C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011748 | |||||||
chr2:55011754 | G | A | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02145.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+13332C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011754 | |||||||
chr2:55011770 | T | C | 1 | a0002c0002t0003g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3013+13316A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011770 | |||||||
chr2:55011914 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3013+13172A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011914 | |||||||
chr2:55011944 | A | G | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+13142T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55011944 | |||||||
chr2:55012066 | G | T | 220 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.3013+13020C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012066 | |||||||
chr2:55012200 | T | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12886A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012200 | |||||||
chr2:55012274 | T | C | 187 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(184): Show |
189 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.3013+12812A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012274 | |||||||
chr2:55012372 | C | A | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12714G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012372 | |||||||
chr2:55012401 | A | T | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+12685T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012401 | |||||||
chr2:55012415 | AC | A | 15 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(12): Show |
15 | HG00140.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.3013+12670delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012415 | |||||||
chr2:55012591 | T | C | 10 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(7): Show |
10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+12495A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012591 | |||||||
chr2:55012682 | A | G | 7 | a0001c0001t0004g0138 a0001c0001t0004g0197 a0001c0001t0004g0199 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.3013+12404T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012682 | |||||||
chr2:55012772 | A | G | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.3013+12314T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012772 | |||||||
chr2:55012890 | A | C | 247 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.3013+12196T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55012890 | |||||||
chr2:55013015 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3013+12071A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013015 | |||||||
chr2:55013210 | G | A | 1 | a0002c0002t0003g0052 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3013+11876C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013210 | |||||||
chr2:55013228 | T | C | 10 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(7): Show |
10 | HG02109.hp1 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+11858A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013228 | |||||||
chr2:55013251 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3013+11835A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013251 | |||||||
chr2:55013276 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3013+11810G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013276 | |||||||
chr2:55013463 | C | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(73): Show |
77 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.3013+11623G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013463 | |||||||
chr2:55013503 | C | T | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3013+11583G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013503 | |||||||
chr2:55013554 | A | T | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11532T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013554 | |||||||
chr2:55013599 | G | GT | 12 | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0124 others(9): Show |
12 | HG01978.hp2 HG02055.hp2 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.3013+11486dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013599 | |||||||
chr2:55013608 | T | G | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11478A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013608 | |||||||
chr2:55013608 | TG | T | 159 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0112 others(156): Show |
165 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.3013+11477delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013608 | |||||||
chr2:55013609 | G | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3013+11477C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013609 | |||||||
chr2:55013610 | G | T | 22 | a0001c0001t0001g0099 a0001c0001t0001g0216 a0001c0001t0001g0273 others(19): Show |
22 | HG01167.hp1 HG02109.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.3013+11476C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013610 | |||||||
chr2:55013622 | G | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.3013+11464C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013622 | |||||||
chr2:55013627 | A | AG | 11 | a0001c0001t0001g0263 a0001c0001t0002g0154 a0001c0001t0002g0156 others(8): Show |
11 | HG01109.hp1 HG01175.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.3013+11458dupC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013627 | |||||||
chr2:55013678 | T | TTAGATTT others(9): Show |
1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+11407_3013+11 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013678 | |||||||
chr2:55013748 | T | G | 1 | a0001c0001t0016g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3013+11338A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55013748 | |||||||
chr2:55014080 | A | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.3013+11006T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014080 | |||||||
chr2:55014159 | A | C | 4 | a0001c0001t0009g0082 a0005c0005t0001g0323 a0005c0005t0001g0325 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+10927T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014159 | |||||||
chr2:55014279 | G | A | 2 | a0004c0004t0002g0009 a0004c0004t0002g0137 |
3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.3013+10807C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014279 | |||||||
chr2:55014522 | A | AT | 123 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(120): Show |
125 | HG00099.hp2 HG00544.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.3013+10563dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014522 | |||||||
chr2:55014550 | G | T | 238 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(235): Show |
243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.3013+10536C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014550 | |||||||
chr2:55014575 | T | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.3013+10511A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014575 | |||||||
chr2:55014613 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.3013+10473C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014613 | |||||||
chr2:55014866 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3013+10220G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55014866 | |||||||
chr2:55015059 | G | A | 3 | a0001c0001t0011g0264 a0001c0001t0011g0267 a0001c0001t0011g0268 |
3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+10027C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015059 | |||||||
chr2:55015133 | C | T | 1 | a0002c0002t0003g0036 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3013+9953G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015133 | |||||||
chr2:55015245 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3013+9841G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015245 | |||||||
chr2:55015320 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(95): Show |
99 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.3013+9766G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015320 | |||||||
chr2:55015327 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0140 a0001c0001t0002g0141 others(2): Show |
6 | HG00438.hp2 HG02080.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+9759C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015327 | |||||||
chr2:55015328 | G | A | 2 | a0004c0004t0002g0009 a0004c0004t0002g0137 |
3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.3013+9758C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015328 | |||||||
chr2:55015555 | G | T | 1 | a0001c0001t0007g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3013+9531C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015555 | |||||||
chr2:55015579 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0307 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3013+9507A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015579 | |||||||
chr2:55015737 | A | G | 1 | a0001c0001t0005g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3013+9349T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015737 | |||||||
chr2:55015859 | T | C | 6 | a0001c0001t0004g0079 a0001c0001t0004g0193 a0001c0001t0004g0194 others(3): Show |
6 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.3013+9227A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55015859 | |||||||
chr2:55016068 | T | A | 31 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(28): Show |
35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+9018A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016068 | |||||||
chr2:55016301 | G | A | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+8785C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016301 | |||||||
chr2:55016347 | C | T | 4 | a0001c0001t0009g0082 a0005c0005t0001g0323 a0005c0005t0001g0325 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+8739G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016347 | |||||||
chr2:55016348 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3013+8738G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016348 | |||||||
chr2:55016490 | C | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+8596G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016490 | |||||||
chr2:55016534 | G | C | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3013+8552C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016534 | |||||||
chr2:55016549 | A | C | 38 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(35): Show |
39 | HG00735.hp2 HG01928.hp2 HG02080.hp1 others(36): Show |
intron_variant | MODIFIER | c.3013+8537T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016549 | |||||||
chr2:55016628 | GAATAA | G | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+8453_3013+845 others(9): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016628 | |||||||
chr2:55016665 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.3013+8421G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016665 | |||||||
chr2:55016667 | G | C | 5 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+8419C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016667 | |||||||
chr2:55016746 | T | A | 1 | a0002c0002t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.3013+8340A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016746 | |||||||
chr2:55016810 | C | A | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+8276G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55016810 | |||||||
chr2:55017064 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0140 a0001c0001t0002g0141 others(2): Show |
6 | HG00438.hp2 HG02080.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+8022G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017064 | |||||||
chr2:55017262 | C | G | 1 | a0002c0002t0002g0047 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3013+7824G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017262 | |||||||
chr2:55017266 | G | A | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+7820C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017266 | |||||||
chr2:55017302 | G | A | 220 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(217): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.3013+7784C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017302 | |||||||
chr2:55017357 | A | G | 3 | a0001c0001t0011g0264 a0001c0001t0011g0267 a0001c0001t0011g0268 |
3 | HG02132.hp2 NA18986.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.3013+7729T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017357 | |||||||
chr2:55017360 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.3013+7726A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017360 | |||||||
chr2:55017402 | A | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(77): Show |
81 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3013+7684T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017402 | |||||||
chr2:55017544 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3013+7542C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017544 | |||||||
chr2:55017566 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3013+7520G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017566 | |||||||
chr2:55017609 | A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3013+7477T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017609 | |||||||
chr2:55017695 | C | A | 26 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(23): Show |
28 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.3013+7391G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017695 | |||||||
chr2:55017846 | C | T | 29 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(26): Show |
30 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3013+7240G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55017846 | |||||||
chr2:55018028 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3013+7058C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018028 | |||||||
chr2:55018041 | T | C | 194 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(191): Show |
196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.3013+7045A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018041 | |||||||
chr2:55018084 | A | G | 291 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(288): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.3013+7002T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018084 | |||||||
chr2:55018143 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3013+6943A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018143 | |||||||
chr2:55018147 | T | C | 5 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+6939A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018147 | |||||||
chr2:55018238 | T | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3013+6848A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018238 | |||||||
chr2:55018531 | GT | G | 55 | a0001c0001t0001g0214 a0001c0001t0004g0077 a0001c0001t0004g0079 others(52): Show |
58 | HG00099.hp2 HG01109.hp1 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.3013+6554delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018531 | |||||||
chr2:55018613 | T | C | 1 | a0001c0001t0005g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3013+6473A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018613 | |||||||
chr2:55018719 | A | G | 1 | a0002c0002t0010g0018 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3013+6367T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55018719 | |||||||
chr2:55019066 | C | G | 31 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(28): Show |
35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+6020G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019066 | |||||||
chr2:55019167 | T | C | 31 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(28): Show |
35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+5919A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019167 | |||||||
chr2:55019287 | A | G | 63 | a0001c0001t0001g0214 a0001c0001t0004g0077 a0001c0001t0004g0079 others(60): Show |
68 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.3013+5799T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019287 | |||||||
chr2:55019306 | G | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0134 a0001c0001t0002g0151 others(8): Show |
12 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.3013+5780C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019306 | |||||||
chr2:55019348 | G | A | 1 | a0001c0001t0005g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3013+5738C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019348 | |||||||
chr2:55019415 | C | T | 250 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(247): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3013+5671G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019415 | |||||||
chr2:55019460 | C | T | 31 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(28): Show |
35 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.3013+5626G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019460 | |||||||
chr2:55019603 | C | T | 31 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(28): Show |
32 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.3013+5483G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019603 | |||||||
chr2:55019651 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.3013+5435C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019651 | |||||||
chr2:55019729 | T | G | 2 | a0001c0001t0002g0145 a0001c0001t0002g0187 |
2 | HG02622.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3013+5357A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019729 | |||||||
chr2:55019780 | T | C | 3 | a0001c0001t0004g0199 a0001c0001t0004g0200 a0001c0001t0004g0201 |
3 | HG03041.hp2 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3013+5306A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019780 | |||||||
chr2:55019935 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3013+5151A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55019935 | |||||||
chr2:55020121 | C | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(66): Show |
70 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.3013+4965G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020121 | |||||||
chr2:55020122 | G | A | 8 | a0001c0001t0004g0138 a0001c0001t0004g0197 a0001c0001t0004g0198 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3013+4964C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020122 | |||||||
chr2:55020130 | C | G | 1 | a0005c0005t0001g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3013+4956G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020130 | |||||||
chr2:55020327 | G | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.3013+4759C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020327 | |||||||
chr2:55020341 | T | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(186): Show |
191 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.3013+4745A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020341 | |||||||
chr2:55020363 | T | C | 5 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.3013+4723A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020363 | |||||||
chr2:55020421 | G | GA | 189 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(186): Show |
191 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.3013+4664dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020421 | |||||||
chr2:55020477 | A | ACTAC | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(86): Show |
90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3013+4605_3013+460 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020477 | |||||||
chr2:55020618 | C | T | 1 | a0001c0001t0002g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3013+4468G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020618 | |||||||
chr2:55020707 | C | G | 7 | a0001c0001t0004g0079 a0001c0001t0004g0193 a0001c0001t0004g0194 others(4): Show |
7 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+4379G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020707 | |||||||
chr2:55020743 | C | A | 4 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+4343G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020743 | |||||||
chr2:55020818 | A | G | 249 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(246): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3013+4268T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55020818 | |||||||
chr2:55021043 | T | C | 4 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+4043A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021043 | |||||||
chr2:55021221 | T | G | 195 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.3013+3865A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021221 | |||||||
chr2:55021325 | G | A | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3013+3761C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021325 | |||||||
chr2:55021391 | G | GC | 40 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(37): Show |
41 | HG00099.hp2 HG01123.hp2 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.3013+3694dupG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021391 | |||||||
chr2:55021394 | C | CG | 89 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0219 others(86): Show |
90 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.3013+3691_3013+369 others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021394 | |||||||
chr2:55021400 | G | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3686C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021400 | |||||||
chr2:55021401 | C | G | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3685G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021401 | |||||||
chr2:55021403 | A | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3013+3683T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021403 | |||||||
chr2:55021466 | C | CT | 8 | a0001c0001t0002g0076 a0001c0001t0002g0222 a0002c0002t0001g0049 others(5): Show |
10 | HG00609.hp1 HG00738.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.3013+3619dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021466 | |||||||
chr2:55021466 | CT | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(79): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.3013+3619delA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021466 | |||||||
chr2:55021512 | G | A | 10 | a0002c0002t0001g0049 a0002c0002t0003g0013 a0002c0002t0003g0015 others(7): Show |
10 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+3574C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021512 | |||||||
chr2:55021543 | G | C | 1 | a0001c0001t0002g0180 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3013+3543C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021543 | |||||||
chr2:55021593 | G | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+3493C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021593 | |||||||
chr2:55021682 | T | C | 35 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(32): Show |
36 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3013+3404A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021682 | |||||||
chr2:55021721 | A | G | 35 | a0001c0001t0001g0214 a0001c0001t0005g0011 a0001c0001t0005g0277 others(32): Show |
36 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.3013+3365T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021721 | |||||||
chr2:55021829 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3013+3257G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55021829 | |||||||
chr2:55022068 | A | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3013+3018T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022068 | |||||||
chr2:55022220 | A | G | 2 | a0001c0001t0009g0164 a0001c0001t0009g0316 |
2 | HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3013+2866T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022220 | |||||||
chr2:55022235 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3013+2851G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022235 | |||||||
chr2:55022346 | T | C | 15 | a0001c0001t0002g0155 a0001c0001t0002g0190 a0001c0001t0009g0164 others(12): Show |
18 | HG00738.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.3013+2740A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022346 | |||||||
chr2:55022554 | A | G | 1 | a0001c0001t0005g0280 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3013+2532T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022554 | |||||||
chr2:55022896 | A | AAC | 18 | a0001c0001t0002g0081 a0001c0001t0002g0133 a0001c0001t0002g0154 others(15): Show |
18 | HG01069.hp2 HG01071.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.3013+2188_3013+218 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACAC | 10 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0002g0152 others(7): Show |
10 | HG00140.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3013+2186_3013+218 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACAC | 3 | a0001c0001t0001g0273 a0001c0001t0005g0278 a0001c0008t0017g0067 |
3 | HG02647.hp1 HG02809.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3013+2184_3013+218 others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(1): Show |
16 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0206 others(13): Show |
16 | HG00099.hp1 HG01175.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.3013+2182_3013+218 others(12): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(3): Show |
3 | a0001c0001t0001g0093 a0001c0001t0001g0262 a0001c0017t0001g0265 |
3 | HG01496.hp1 HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.3013+2180_3013+218 others(14): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(5): Show |
45 | a0001c0001t0001g0006 a0001c0001t0001g0075 a0001c0001t0001g0078 others(42): Show |
46 | HG00558.hp2 HG00741.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.3013+2178_3013+218 others(16): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(7): Show |
15 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0103 others(12): Show |
15 | HG00323.hp2 HG00423.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.3013+2176_3013+218 others(18): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(9): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0121 others(1): Show |
4 | HG00544.hp1 HG02559.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013+2174_3013+218 others(20): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(11): Show |
29 | a0001c0001t0001g0010 a0001c0001t0001g0219 a0001c0001t0001g0223 others(26): Show |
30 | HG00735.hp2 HG01070.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.3013+2172_3013+218 others(22): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(13): Show |
16 | a0001c0001t0001g0120 a0001c0001t0001g0243 a0001c0001t0001g0250 others(13): Show |
16 | HG00735.hp1 HG00738.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.3013+2170_3013+218 others(24): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(15): Show |
25 | a0001c0001t0001g0225 a0001c0001t0001g0237 a0001c0001t0001g0238 others(22): Show |
25 | HG00642.hp1 HG01167.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.3013+2168_3013+218 others(26): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(17): Show |
10 | a0001c0001t0001g0224 a0001c0001t0001g0230 a0001c0001t0001g0234 others(7): Show |
10 | HG00544.hp2 HG01074.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.3013+2166_3013+218 others(28): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(19): Show |
6 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0236 others(3): Show |
6 | HG02148.hp1 NA18952.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.3013+2164_3013+218 others(30): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | AACACACA others(21): Show |
1 | a0013c0014t0001g0244 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3013+2162_3013+218 others(32): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022896 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3013+2189_3013+219 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022896 | |||||||
chr2:55022930 | C | CACACACA others(6): Show |
1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3013+2155_3013+215 others(17): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022930 | |||||||
chr2:55022930 | C | CACACACA others(12): Show |
2 | a0001c0001t0001g0252 a0002c0002t0003g0053 |
2 | HG04184.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.3013+2155_3013+215 others(23): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022930 | |||||||
chr2:55022985 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3013+2101T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55022985 | |||||||
chr2:55023258 | G | T | 1 | a0001c0001t0007g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3013+1828C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023258 | |||||||
chr2:55023485 | A | G | 1 | a0002c0002t0003g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3013+1601T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023485 | |||||||
chr2:55023610 | G | A | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.3013+1476C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55023610 | |||||||
chr2:55024071 | T | C | 32 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0005g0011 others(29): Show |
33 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.3013+1015A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024071 | |||||||
chr2:55024089 | T | C | 1 | a0001c0001t0011g0268 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3013+997A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024089 | |||||||
chr2:55024095 | C | T | 30 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(27): Show |
32 | HG00738.hp1 HG01109.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.3013+991G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024095 | |||||||
chr2:55024216 | C | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3013+870G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024216 | |||||||
chr2:55024238 | G | A | 134 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.3013+848C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024238 | |||||||
chr2:55024331 | G | A | 19 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(16): Show |
19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3013+755C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024331 | |||||||
chr2:55024375 | C | G | 50 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.3013+711G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024375 | |||||||
chr2:55024415 | C | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3013+671G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024415 | |||||||
chr2:55024468 | A | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3013+618T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024468 | |||||||
chr2:55024505 | A | G | 4 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.3013+581T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024505 | |||||||
chr2:55024585 | T | C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
7 | NA18951.hp1 NA18971.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.3013+501A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024585 | |||||||
chr2:55024654 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3013+432T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024654 | |||||||
chr2:55024705 | T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3013+381A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024705 | |||||||
chr2:55024975 | A | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3013+111T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55024975 | |||||||
chr2:55025041 | C | T | 23 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(20): Show |
25 | HG00738.hp1 HG01109.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.3013+45G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025041 | |||||||
chr2:55025058 | G | A | 1 | a0001c0001t0002g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3013+28C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025058 | |||||||
chr2:55025078 | T | G | 35 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(32): Show |
36 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(33): Show |
splice_region_variant&intron_variant | LOW | c.3013+8A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 3/8 | chr2 | 55025078 | |||||||
chr2:55027567 | G | A | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-82C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027567 | |||||||
chr2:55027585 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0219 a0001c0001t0001g0223 others(16): Show |
20 | HG00735.hp2 HG01928.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.614-100A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027585 | |||||||
chr2:55027667 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.614-182A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027667 | |||||||
chr2:55027678 | CAT | C | 17 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(14): Show |
17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.614-195_614-194del others(2): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027678 | |||||||
chr2:55027717 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.614-232C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027717 | |||||||
chr2:55027970 | G | A | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02040.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.613+194C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 2/8 | chr2 | 55027970 | |||||||
chr2:55028523 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.557-303T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028523 | |||||||
chr2:55028587 | C | T | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-367G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028587 | |||||||
chr2:55028660 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0002g0274 |
3 | HG00140.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.557-440G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028660 | |||||||
chr2:55028734 | C | T | 287 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(284): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.557-514G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028734 | |||||||
chr2:55028787 | CA | C | 227 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(224): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.557-568delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028787 | |||||||
chr2:55028799 | A | T | 247 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0074 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.557-579T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028799 | |||||||
chr2:55028863 | A | G | 1 | a0001c0001t0021g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.557-643T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028863 | |||||||
chr2:55028962 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.557-742T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55028962 | |||||||
chr2:55029007 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-787A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029007 | |||||||
chr2:55029105 | AC | A | 5 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0023t0001g0322 others(2): Show |
5 | HG02040.hp2 HG02165.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-886delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029105 | |||||||
chr2:55029277 | A | C | 1 | a0001c0001t0002g0070 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.557-1057T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029277 | |||||||
chr2:55029518 | T | C | 1 | a0001c0001t0006g0304 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.557-1298A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029518 | |||||||
chr2:55029591 | A | G | 4 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0029 others(1): Show |
4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-1371T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55029591 | |||||||
chr2:55030062 | T | C | 2 | a0001c0001t0005g0287 a0001c0001t0005g0288 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.557-1842A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030062 | |||||||
chr2:55030099 | G | C | 1 | a0016c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.557-1879C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030099 | |||||||
chr2:55030149 | T | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-1929A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030149 | |||||||
chr2:55030273 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(79): Show |
83 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.557-2053A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030273 | |||||||
chr2:55030351 | T | C | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.557-2131A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030351 | |||||||
chr2:55030450 | G | T | 29 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(26): Show |
30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.557-2230C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030450 | |||||||
chr2:55030453 | T | C | 1 | a0001c0001t0005g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.557-2233A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030453 | |||||||
chr2:55030541 | C | T | 63 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(60): Show |
64 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.557-2321G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55030541 | |||||||
chr2:55031018 | AC | A | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.557-2799delG | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031018 | |||||||
chr2:55031059 | C | T | 19 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(16): Show |
19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-2839G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031059 | |||||||
chr2:55031241 | C | T | 19 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(16): Show |
19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-3021G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031241 | |||||||
chr2:55031421 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.557-3201T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031421 | |||||||
chr2:55031568 | C | G | 59 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.557-3348G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031568 | |||||||
chr2:55031710 | C | G | 4 | a0002c0002t0003g0027 a0002c0002t0003g0028 a0002c0002t0003g0029 others(1): Show |
4 | NA18952.hp1 NA18960.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-3490G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031710 | |||||||
chr2:55031715 | T | C | 2 | a0001c0001t0016g0313 a0002c0002t0002g0060 |
2 | HG03195.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.557-3495A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031715 | |||||||
chr2:55031789 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.557-3569C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031789 | |||||||
chr2:55031815 | C | A | 1 | a0006c0006t0002g0302 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.557-3595G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031815 | |||||||
chr2:55031993 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.557-3773A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55031993 | |||||||
chr2:55032023 | T | C | 1 | a0001c0001t0007g0333 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.557-3803A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032023 | |||||||
chr2:55032056 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.557-3836G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032056 | |||||||
chr2:55032133 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.557-3913A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032133 | |||||||
chr2:55032159 | C | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.557-3939G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032159 | |||||||
chr2:55032544 | A | G | 19 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(16): Show |
19 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.557-4324T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032544 | |||||||
chr2:55032602 | T | A | 1 | a0001c0001t0002g0182 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-4382A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032602 | |||||||
chr2:55032603 | T | C | 1 | a0001c0001t0002g0182 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.557-4383A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032603 | |||||||
chr2:55032612 | A | T | 94 | a0001c0001t0001g0010 a0001c0001t0001g0219 a0001c0001t0001g0223 others(91): Show |
95 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.557-4392T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032612 | |||||||
chr2:55032785 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.557-4565A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032785 | |||||||
chr2:55032791 | G | A | 3 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 |
3 | HG02818.hp2 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.557-4571C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55032791 | |||||||
chr2:55033050 | T | TA | 63 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(60): Show |
66 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.557-4831dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033050 | |||||||
chr2:55033050 | TA | T | 7 | a0001c0001t0001g0084 a0001c0001t0001g0226 a0001c0001t0002g0132 others(4): Show |
7 | HG00323.hp1 HG01257.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-4831delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033050 | |||||||
chr2:55033057 | A | G | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.557-4837T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033057 | |||||||
chr2:55033161 | A | C | 1 | a0007c0007t0004g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.557-4941T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033161 | |||||||
chr2:55033277 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.557-5057A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033277 | |||||||
chr2:55033426 | C | G | 14 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0273 others(11): Show |
14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.557-5206G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033426 | |||||||
chr2:55033498 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.557-5278A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033498 | |||||||
chr2:55033511 | G | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(51): Show |
55 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.557-5291C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033511 | |||||||
chr2:55033596 | G | A | 8 | a0001c0001t0002g0190 a0001c0001t0007g0332 a0001c0001t0007g0333 others(5): Show |
8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-5376C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033596 | |||||||
chr2:55033807 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.557-5587A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033807 | |||||||
chr2:55033810 | G | A | 29 | a0001c0001t0005g0011 a0001c0001t0005g0278 a0001c0001t0005g0279 others(26): Show |
30 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.557-5590C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033810 | |||||||
chr2:55033921 | T | C | 1 | a0002c0002t0003g0019 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.557-5701A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033921 | |||||||
chr2:55033955 | C | T | 1 | a0001c0001t0009g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.557-5735G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55033955 | |||||||
chr2:55034161 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.557-5941A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034161 | |||||||
chr2:55034351 | C | A | 238 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(235): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.557-6131G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034351 | |||||||
chr2:55034496 | T | C | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-6276A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034496 | |||||||
chr2:55034523 | T | C | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.557-6303A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034523 | |||||||
chr2:55034603 | T | A | 1 | a0001c0001t0009g0082 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.557-6383A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034603 | |||||||
chr2:55034795 | T | A | 247 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(244): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.557-6575A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55034795 | |||||||
chr2:55035002 | A | G | 2 | a0001c0001t0002g0183 a0001c0001t0023g0150 |
2 | HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.557-6782T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035002 | |||||||
chr2:55035023 | C | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.557-6803G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035023 | |||||||
chr2:55035174 | G | A | 5 | a0001c0001t0001g0216 a0001c0001t0001g0273 a0001c0001t0001g0275 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-6954C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035174 | |||||||
chr2:55035229 | T | G | 1 | a0001c0001t0002g0183 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.557-7009A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035229 | |||||||
chr2:55035368 | G | A | 1 | a0001c0001t0002g0148 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.557-7148C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035368 | |||||||
chr2:55035409 | AG | A | 17 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(14): Show |
17 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.557-7190delC | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035409 | |||||||
chr2:55035411 | G | T | 1 | a0001c0001t0005g0294 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.557-7191C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035411 | |||||||
chr2:55035478 | TAGAG | T | 4 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0021 others(1): Show |
4 | HG00544.hp2 HG02083.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-7262_557-7259d others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035478 | |||||||
chr2:55035488 | T | C | 1 | a0002c0002t0003g0048 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.557-7268A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035488 | |||||||
chr2:55035529 | G | A | 10 | a0002c0002t0001g0049 a0002c0002t0003g0013 a0002c0002t0003g0015 others(7): Show |
10 | HG01070.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.557-7309C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035529 | |||||||
chr2:55035625 | TA | T | 13 | a0001c0001t0001g0103 a0001c0001t0001g0119 a0001c0001t0001g0120 others(10): Show |
13 | HG01069.hp1 HG01167.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.557-7406delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035625 | |||||||
chr2:55035656 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.557-7436G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035656 | |||||||
chr2:55035696 | T | C | 1 | a0016c0019t0001g0269 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.557-7476A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035696 | |||||||
chr2:55035727 | G | C | 1 | a0005c0005t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.557-7507C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035727 | |||||||
chr2:55035823 | C | A | 1 | a0005c0005t0001g0330 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.557-7603G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035823 | |||||||
chr2:55035849 | T | G | 2 | a0001c0001t0005g0290 a0001c0001t0005g0291 |
2 | HG00099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.557-7629A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55035849 | |||||||
chr2:55036007 | C | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(125): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.557-7787G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036007 | |||||||
chr2:55036324 | G | T | 1 | a0011c0015t0008g0308 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.557-8104C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036324 | |||||||
chr2:55036471 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.557-8251C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036471 | |||||||
chr2:55036564 | T | C | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-8344A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036564 | |||||||
chr2:55036599 | C | CA | 54 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(51): Show |
55 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.557-8380dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036599 | C | CAA | 7 | a0001c0001t0001g0119 a0001c0001t0001g0263 a0001c0001t0002g0292 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.557-8381_557-8380d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036599 | CA | C | 80 | a0001c0001t0001g0214 a0001c0001t0001g0219 a0001c0001t0001g0224 others(77): Show |
82 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.557-8380delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036599 | CAA | C | 46 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0087 others(43): Show |
46 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.557-8381_557-8380d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036599 | CAAA | C | 27 | a0001c0001t0001g0086 a0001c0001t0005g0011 a0001c0001t0005g0277 others(24): Show |
30 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.557-8382_557-8380d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036599 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0010 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
7 | NA18951.hp1 NA18971.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.557-8387_557-8380d others(10): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036599 | |||||||
chr2:55036622 | AAAT | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(68): Show |
78 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.557-8405_557-8403d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036622 | |||||||
chr2:55036627 | A | T | 157 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(154): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.557-8407T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036627 | |||||||
chr2:55036673 | T | C | 34 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(31): Show |
37 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.557-8453A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036673 | |||||||
chr2:55036706 | G | T | 14 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0273 others(11): Show |
14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.557-8486C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036706 | |||||||
chr2:55036882 | A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-8662T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036882 | |||||||
chr2:55036968 | C | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0129 |
2 | NA18950.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.557-8748G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55036968 | |||||||
chr2:55037139 | A | G | 12 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(9): Show |
14 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.557-8919T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037139 | |||||||
chr2:55037197 | T | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.557-8977A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037197 | |||||||
chr2:55037314 | T | C | 1 | a0001c0012t0004g0213 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.557-9094A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037314 | |||||||
chr2:55037389 | A | G | 8 | a0001c0001t0002g0190 a0001c0001t0007g0332 a0001c0001t0007g0333 others(5): Show |
8 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-9169T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037389 | |||||||
chr2:55037430 | T | C | 4 | a0001c0001t0004g0138 a0001c0001t0004g0197 a0001c0001t0004g0202 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.557-9210A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037430 | |||||||
chr2:55037567 | T | C | 6 | a0001c0001t0002g0002 a0001c0001t0002g0207 a0001c0001t0002g0208 others(3): Show |
8 | HG00423.hp2 HG00621.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.557-9347A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037567 | |||||||
chr2:55037723 | C | G | 102 | a0001c0001t0001g0181 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
109 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.557-9503G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037723 | |||||||
chr2:55037823 | A | C | 3 | a0001c0001t0005g0278 a0001c0001t0005g0279 a0001c0001t0005g0280 |
3 | HG02647.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557-9603T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037823 | |||||||
chr2:55037825 | G | C | 38 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(35): Show |
41 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.557-9605C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037825 | |||||||
chr2:55037961 | T | C | 1 | a0001c0001t0007g0334 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.557-9741A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55037961 | |||||||
chr2:55038062 | A | C | 1 | a0001c0001t0002g0147 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.557-9842T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038062 | |||||||
chr2:55038067 | C | G | 238 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(235): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.557-9847G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038067 | |||||||
chr2:55038076 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.557-9856A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038076 | |||||||
chr2:55038332 | G | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.557-10112C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038332 | |||||||
chr2:55038498 | C | CAT | 110 | a0001c0001t0001g0181 a0001c0001t0002g0001 a0001c0001t0002g0002 others(107): Show |
119 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.557-10279_557-1027 others(6): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038498 | |||||||
chr2:55038516 | A | G | 1 | a0001c0001t0004g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.557-10296T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038516 | |||||||
chr2:55038649 | C | T | 137 | a0001c0001t0001g0181 a0001c0001t0002g0001 a0001c0001t0002g0002 others(134): Show |
147 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.557-10429G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038649 | |||||||
chr2:55038688 | A | G | 1 | a0001c0001t0004g0198 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.557-10468T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038688 | |||||||
chr2:55038891 | C | G | 1 | a0001c0001t0014g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.557-10671G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038891 | |||||||
chr2:55038900 | G | T | 1 | a0001c0001t0009g0068 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.557-10680C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038900 | |||||||
chr2:55038930 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.557-10710A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038930 | |||||||
chr2:55038970 | T | A | 5 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(2): Show |
5 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.557-10750A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55038970 | |||||||
chr2:55039052 | A | G | 1 | a0001c0001t0011g0264 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.556+10693T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039052 | |||||||
chr2:55039074 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.556+10671A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039074 | |||||||
chr2:55039384 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.556+10361G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039384 | |||||||
chr2:55039453 | AAAAG | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0127 |
3 | HG02559.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.556+10288_556+1029 others(8): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039453 | |||||||
chr2:55039520 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.556+10225G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039520 | |||||||
chr2:55039535 | T | G | 7 | a0001c0001t0007g0332 a0001c0001t0007g0333 a0001c0001t0007g0334 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+10210A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039535 | |||||||
chr2:55039559 | C | T | 60 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(57): Show |
65 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.556+10186G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039559 | |||||||
chr2:55039647 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.556+10098A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039647 | |||||||
chr2:55039819 | T | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+9926A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039819 | |||||||
chr2:55039881 | A | T | 1 | a0005c0005t0001g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.556+9864T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55039881 | |||||||
chr2:55040017 | T | A | 34 | a0001c0001t0005g0011 a0001c0001t0005g0278 a0001c0001t0005g0279 others(31): Show |
37 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.556+9728A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040017 | |||||||
chr2:55040066 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.556+9679A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040066 | |||||||
chr2:55040073 | A | G | 1 | a0001c0001t0005g0278 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.556+9672T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040073 | |||||||
chr2:55040404 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.556+9341A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040404 | |||||||
chr2:55040409 | T | C | 109 | a0001c0001t0001g0181 a0001c0001t0002g0001 a0001c0001t0002g0002 others(106): Show |
118 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.556+9336A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040409 | |||||||
chr2:55040460 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.556+9285G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040460 | |||||||
chr2:55040469 | C | T | 27 | a0001c0001t0004g0077 a0001c0001t0004g0079 a0001c0001t0004g0138 others(24): Show |
29 | HG01109.hp1 HG01346.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.556+9276G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040469 | |||||||
chr2:55040472 | T | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | NA18987.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.556+9273A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040472 | |||||||
chr2:55040555 | G | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+9190C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040555 | |||||||
chr2:55040990 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556+8755C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55040990 | |||||||
chr2:55041000 | T | TA | 6 | a0001c0001t0001g0252 a0001c0001t0003g0131 a0001c0008t0008g0259 others(3): Show |
6 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.556+8744dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041000 | |||||||
chr2:55041000 | TA | T | 144 | a0001c0001t0001g0181 a0001c0001t0001g0214 a0001c0001t0001g0253 others(141): Show |
156 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.556+8744delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041000 | |||||||
chr2:55041055 | G | T | 50 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.556+8690C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041055 | |||||||
chr2:55041080 | A | AT | 61 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(58): Show |
64 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.556+8664dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041080 | |||||||
chr2:55041233 | A | T | 1 | a0001c0001t0005g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.556+8512T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041233 | |||||||
chr2:55041242 | T | C | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+8503A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041242 | |||||||
chr2:55041277 | G | C | 1 | a0001c0001t0002g0102 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.556+8468C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041277 | |||||||
chr2:55041334 | T | G | 1 | a0006c0006t0022g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.556+8411A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041334 | |||||||
chr2:55041441 | C | G | 13 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0273 others(10): Show |
13 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+8304G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041441 | |||||||
chr2:55041550 | T | C | 1 | a0001c0001t0002g0185 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.556+8195A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041550 | |||||||
chr2:55041595 | G | A | 4 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+8150C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041595 | |||||||
chr2:55041683 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556+8062T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041683 | |||||||
chr2:55041716 | T | G | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+8029A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041716 | |||||||
chr2:55041902 | G | T | 13 | a0001c0001t0001g0214 a0001c0001t0001g0216 a0001c0001t0001g0273 others(10): Show |
13 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+7843C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041902 | |||||||
chr2:55041917 | T | G | 1 | a0001c0001t0012g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.556+7828A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55041917 | |||||||
chr2:55042013 | T | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(239): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.556+7732A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042013 | |||||||
chr2:55042061 | T | A | 1 | a0004c0004t0002g0191 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.556+7684A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042061 | |||||||
chr2:55042252 | A | C | 170 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(167): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.556+7493T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042252 | |||||||
chr2:55042285 | A | G | 1 | a0002c0002t0003g0025 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.556+7460T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042285 | |||||||
chr2:55042546 | G | A | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+7199C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042546 | |||||||
chr2:55042594 | G | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+7151C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042594 | |||||||
chr2:55042673 | G | A | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+7072C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042673 | |||||||
chr2:55042713 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.556+7032T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042713 | |||||||
chr2:55042750 | T | A | 239 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(236): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.556+6995A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042750 | |||||||
chr2:55042773 | T | C | 2 | a0004c0004t0002g0009 a0004c0004t0002g0137 |
3 | HG01070.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.556+6972A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042773 | |||||||
chr2:55042812 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(127): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.556+6933G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55042812 | |||||||
chr2:55043016 | T | C | 1 | a0001c0001t0004g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.556+6729A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043016 | |||||||
chr2:55043038 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+6707T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043038 | |||||||
chr2:55043071 | G | A | 1 | a0003c0003t0004g0073 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.556+6674C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043071 | |||||||
chr2:55043172 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.556+6573G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043172 | |||||||
chr2:55043187 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+6558A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043187 | |||||||
chr2:55043349 | T | G | 83 | a0001c0001t0001g0181 a0001c0001t0001g0253 a0001c0001t0002g0001 others(80): Show |
90 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.556+6396A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043349 | |||||||
chr2:55043493 | C | T | 82 | a0001c0001t0001g0181 a0001c0001t0002g0001 a0001c0001t0002g0002 others(79): Show |
89 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.556+6252G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043493 | |||||||
chr2:55043580 | C | T | 2 | a0001c0001t0004g0138 a0001c0001t0004g0197 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.556+6165G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043580 | |||||||
chr2:55043668 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(135): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+6077G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043668 | |||||||
chr2:55043711 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.556+6034G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043711 | |||||||
chr2:55043776 | C | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+5969G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043776 | |||||||
chr2:55043777 | T | G | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+5968A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043777 | |||||||
chr2:55043839 | T | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(76): Show |
80 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.556+5906A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55043839 | |||||||
chr2:55044052 | C | T | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+5693G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044052 | |||||||
chr2:55044057 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.556+5688C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044057 | |||||||
chr2:55044090 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+5655C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044090 | |||||||
chr2:55044227 | T | A | 1 | a0005c0005t0001g0327 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.556+5518A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044227 | |||||||
chr2:55044228 | T | A | 227 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(224): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.556+5517A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044228 | |||||||
chr2:55044285 | G | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0255 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.556+5460C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044285 | |||||||
chr2:55044399 | C | G | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+5346G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044399 | |||||||
chr2:55044403 | C | G | 7 | a0003c0003t0004g0004 a0003c0003t0004g0005 a0003c0003t0004g0073 others(4): Show |
9 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.556+5342G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044403 | |||||||
chr2:55044407 | C | G | 1 | a0003c0003t0013g0071 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.556+5338G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044407 | |||||||
chr2:55044419 | C | A | 13 | a0001c0001t0004g0077 a0001c0001t0004g0138 a0001c0001t0004g0139 others(10): Show |
13 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.556+5326G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044419 | |||||||
chr2:55044445 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(100): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.556+5300A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044445 | |||||||
chr2:55044487 | G | T | 4 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+5258C>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044487 | |||||||
chr2:55044670 | T | C | 1 | a0001c0001t0005g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.556+5075A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044670 | |||||||
chr2:55044683 | T | C | 1 | a0001c0013t0001g0122 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.556+5062A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044683 | |||||||
chr2:55044735 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5010A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044735 | |||||||
chr2:55044737 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5008A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044737 | |||||||
chr2:55044739 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(135): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+5006G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044739 | |||||||
chr2:55044741 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+5004G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044741 | |||||||
chr2:55044746 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4999G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044746 | |||||||
chr2:55044747 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4998A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044747 | |||||||
chr2:55044749 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.556+4996G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044749 | |||||||
chr2:55044785 | T | TA | 78 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(75): Show |
85 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.556+4959dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | |||||||
chr2:55044785 | T | TAA | 105 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(102): Show |
109 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.556+4958_556+4959d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | |||||||
chr2:55044785 | T | TAAA | 23 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG01123.hp2 HG01346.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.556+4957_556+4959d others(5): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | |||||||
chr2:55044785 | TA | T | 34 | a0001c0001t0001g0219 a0001c0001t0001g0224 a0001c0001t0001g0273 others(31): Show |
36 | HG00140.hp1 HG01167.hp1 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.556+4959delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044785 | |||||||
chr2:55044829 | C | G | 138 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(135): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.556+4916G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55044829 | |||||||
chr2:55045012 | T | C | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | NA18952.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.556+4733A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045012 | |||||||
chr2:55045087 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.556+4658G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045087 | |||||||
chr2:55045153 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.556+4592T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045153 | |||||||
chr2:55045201 | A | T | 4 | a0001c0008t0008g0259 a0001c0008t0008g0260 a0001c0008t0008g0261 others(1): Show |
4 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+4544T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045201 | |||||||
chr2:55045295 | C | T | 1 | a0001c0001t0024g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.556+4450G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045295 | |||||||
chr2:55045474 | T | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.556+4271A>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045474 | |||||||
chr2:55045548 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.556+4197A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045548 | |||||||
chr2:55045905 | C | T | 2 | a0001c0001t0004g0079 a0001c0001t0004g0217 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.556+3840G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55045905 | |||||||
chr2:55046045 | A | T | 51 | a0001c0001t0005g0011 a0001c0001t0005g0277 a0001c0001t0005g0278 others(48): Show |
56 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.556+3700T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046045 | |||||||
chr2:55046094 | GTAAACAG others(6): Show |
G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0207 a0001c0001t0002g0208 others(3): Show |
8 | HG00423.hp2 HG00621.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.556+3638_556+3650d others(15): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046094 | |||||||
chr2:55046151 | C | T | 289 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(286): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.556+3594G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046151 | |||||||
chr2:55046261 | A | G | 6 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0002c0002t0003g0019 others(3): Show |
6 | HG00544.hp2 HG02040.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.556+3484T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046261 | |||||||
chr2:55046357 | C | T | 10 | a0005c0005t0001g0323 a0005c0005t0001g0324 a0005c0005t0001g0325 others(7): Show |
10 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.556+3388G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046357 | |||||||
chr2:55046667 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.556+3078G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046667 | |||||||
chr2:55046747 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.556+2998A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046747 | |||||||
chr2:55046792 | T | C | 7 | a0001c0001t0001g0216 a0007c0007t0004g0062 a0007c0007t0004g0063 others(4): Show |
7 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.556+2953A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046792 | |||||||
chr2:55046836 | A | C | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.556+2909T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046836 | |||||||
chr2:55046931 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.556+2814A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55046931 | |||||||
chr2:55047161 | C | G | 1 | a0001c0001t0001g0078 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.556+2584G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047161 | |||||||
chr2:55047202 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.556+2543G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047202 | |||||||
chr2:55047266 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.556+2479C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047266 | |||||||
chr2:55047327 | C | CA | 7 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0008t0008g0259 others(4): Show |
7 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+2417dupT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | |||||||
chr2:55047327 | CA | C | 82 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0219 others(79): Show |
86 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.556+2417delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | |||||||
chr2:55047327 | CAA | C | 24 | a0001c0001t0002g0292 a0001c0001t0005g0011 a0001c0001t0005g0278 others(21): Show |
25 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.556+2416_556+2417d others(4): Show |
RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047327 | |||||||
chr2:55047395 | C | T | 49 | a0002c0002t0001g0049 a0002c0002t0001g0056 a0002c0002t0002g0047 others(46): Show |
49 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.556+2350G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047395 | |||||||
chr2:55047509 | C | T | 1 | a0001c0001t0016g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.556+2236G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047509 | |||||||
chr2:55047575 | GA | G | 292 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0075 others(289): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.556+2169delT | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047575 | |||||||
chr2:55047771 | T | C | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+1974A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047771 | |||||||
chr2:55047828 | C | T | 1 | a0010c0024t0006g0331 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.556+1917G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047828 | |||||||
chr2:55047881 | T | A | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1864A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047881 | |||||||
chr2:55047882 | G | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1863C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047882 | |||||||
chr2:55047884 | A | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1861T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047884 | |||||||
chr2:55047886 | G | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1859C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047886 | |||||||
chr2:55047887 | A | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1858T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047887 | |||||||
chr2:55047888 | A | C | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1857T>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047888 | |||||||
chr2:55047889 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1856G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047889 | |||||||
chr2:55047890 | T | A | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1855A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047890 | |||||||
chr2:55047892 | G | C | 51 | a0001c0001t0001g0307 a0001c0001t0002g0292 a0001c0001t0005g0011 others(48): Show |
54 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.556+1853C>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047892 | |||||||
chr2:55047894 | A | G | 8 | a0001c0008t0017g0067 a0003c0003t0004g0004 a0003c0003t0004g0005 others(5): Show |
10 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.556+1851T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047894 | |||||||
chr2:55047896 | A | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1849T>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047896 | |||||||
chr2:55047897 | C | T | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+1848G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047897 | |||||||
chr2:55047938 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.556+1807C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55047938 | |||||||
chr2:55048192 | G | A | 11 | a0001c0001t0001g0263 a0001c0001t0001g0266 a0001c0001t0001g0270 others(8): Show |
11 | HG00423.hp1 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.556+1553C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048192 | |||||||
chr2:55048261 | T | C | 2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.556+1484A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048261 | |||||||
chr2:55048424 | G | A | 4 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00140.hp1 HG02145.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.556+1321C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048424 | |||||||
chr2:55048476 | T | A | 38 | a0001c0001t0001g0307 a0001c0001t0002g0292 a0001c0001t0005g0011 others(35): Show |
41 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.556+1269A>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048476 | |||||||
chr2:55048490 | G | A | 1 | a0001c0001t0002g0311 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.556+1255C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048490 | |||||||
chr2:55048500 | A | AT | 56 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0007g0332 others(53): Show |
56 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.556+1244dupA | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048500 | |||||||
chr2:55048732 | A | G | 1 | a0005c0005t0001g0323 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.556+1013T>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048732 | |||||||
chr2:55048926 | C | G | 1 | a0001c0008t0017g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.556+819G>C | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55048926 | |||||||
chr2:55049070 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.556+675C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049070 | |||||||
chr2:55049086 | C | A | 1 | a0001c0001t0016g0313 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.556+659G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049086 | |||||||
chr2:55049094 | C | T | 5 | a0007c0007t0004g0062 a0007c0007t0004g0063 a0007c0007t0004g0066 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+651G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049094 | |||||||
chr2:55049361 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.556+384C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049361 | |||||||
chr2:55049430 | C | A | 1 | a0012c0020t0002g0315 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.556+315G>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049430 | |||||||
chr2:55049522 | T | C | 1 | a0001c0021t0007g0336 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.556+223A>G | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049522 | |||||||
chr2:55049558 | C | T | 5 | a0005c0005t0001g0323 a0005c0005t0001g0324 a0005c0005t0001g0325 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+187G>A | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049558 | |||||||
chr2:55049667 | G | A | 1 | a0001c0001t0009g0316 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.556+78C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049667 | |||||||
chr2:55049719 | G | A | 2 | a0003c0003t0004g0317 a0003c0003t0004g0318 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.556+26C>T | RTN4 | ENSG00000115310.19 | transcript | ENST00000337526.11 | protein_coding | 1/8 | chr2 | 55049719 |