Item | Value |
---|---|
geneid | 8408 |
ensemblid | ENSG00000177169.10 |
hgncid | 12558 |
symbol | ULK1 |
name | unc-51 like autophagy activating kinase 1 |
refseq_nuc | NM_003565.4 |
refseq_prot | NP_003556.2 |
ensembl_nuc | ENST00000321867.6 |
ensembl_prot | ENSP00000324560.3 |
mane_status | MANE Select |
chr | chr12 |
start | 131894622 |
end | 131923150 |
strand | + |
ver | v1.2 |
region | chr12:131894622-131923150 |
region5000 | chr12:131889622-131928150 |
regionname0 | ULK1_chr12_131894622_131923150 |
regionname5000 | ULK1_chr12_131889622_131928150 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1050 | 289 | 85 | 44 | 120 | 10 | 29 | 94 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0002 | 0/0 | 1050 | 43 | 10 | 16 | 5 | 3 | 9 | 4 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0003 | 0/0 | 1050 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0004 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0005 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0006 | 0/0 | 1050 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0007 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0008 | 0/0 | 1050 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0009 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0010 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
a0011 | 0/0 | 1061 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1056): Show |
chr12 | 131889622 | 131928150 |
a0012 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1039): Show |
chr12 | 131889622 | 131928150 |
a0013 | 0/1 | 1050 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | MEPGR others(1045): Show |
chr12 | 131889622 | 131928150 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3150 | 81 | 19 | 9 | 37 | 6 | 10 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0002 | 0/0 | 3150 | 80 | 45 | 14 | 18 | 1 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0003 | 1/0 | 3150 | 75 | 10 | 5 | 50 | 1 | 8 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0005 | 0/0 | 3150 | 14 | 1 | 4 | 9 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0006 | 0/0 | 3150 | 10 | 0 | 5 | 0 | 1 | 4 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0007 | 0/0 | 3150 | 8 | 6 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0009 | 0/0 | 3150 | 5 | 0 | 0 | 3 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0010 | 0/0 | 3150 | 4 | 0 | 2 | 0 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0012 | 0/0 | 3150 | 2 | 0 | 0 | 2 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0013 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0018 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0019 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0020 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0021 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0022 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0023 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0030 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0032 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0001c0035 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0004 | 0/0 | 3150 | 29 | 6 | 11 | 2 | 2 | 8 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0008 | 0/0 | 3150 | 8 | 4 | 4 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0011 | 0/0 | 3150 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0025 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0031 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0002c0033 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0003c0014 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0003c0027 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0004c0016 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0005c0034 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0006c0036 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0007c0015 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0008c0026 | 0/0 | 3150 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0009c0024 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0010c0028 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 | ||
a0011c0037 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3178): Show |
chr12 | 131889622 | 131928150 | ||
a0012c0017 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3127): Show |
chr12 | 131889622 | 131928150 | ||
a0013c0029 | 0/1 | 3150 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | ATGGA others(3145): Show |
chr12 | 131889622 | 131928150 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5322 | 23 | 18 | 1 | 3 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0002 | 0/0 | 5322 | 50 | 1 | 8 | 29 | 5 | 7 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0003 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0007 | 0/0 | 5323 | 2 | 0 | 0 | 1 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0015 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0017 | 0/0 | 5323 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0020 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0021 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0001t0026 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0001 | 0/0 | 5322 | 67 | 36 | 11 | 17 | 1 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0002 | 0/0 | 5322 | 8 | 6 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0003 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0004 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0011 | 0/0 | 5323 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0013 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0002t0019 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0001 | 0/0 | 5322 | 2 | 0 | 0 | 1 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0002 | 0/0 | 5322 | 6 | 5 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0003 | 1/0 | 5322 | 50 | 3 | 5 | 35 | 1 | 5 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0006 | 0/0 | 5323 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0008 | 0/0 | 5322 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0009 | 0/0 | 5322 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0010 | 0/0 | 5322 | 2 | 0 | 0 | 0 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0012 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0014 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0016 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0018 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0003t0024 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0005t0001 | 0/0 | 5322 | 12 | 1 | 4 | 7 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0005t0002 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0006t0002 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0006t0003 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0006t0004 | 0/0 | 5322 | 7 | 0 | 3 | 0 | 1 | 3 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0006t0028 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0007t0001 | 0/0 | 5322 | 7 | 5 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0007t0011 | 0/0 | 5323 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0001c0009t0005 | 0/0 | 5322 | 5 | 0 | 0 | 3 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0010t0002 | 0/0 | 5322 | 3 | 0 | 2 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0010t0004 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0012t0001 | 0/0 | 5322 | 2 | 0 | 0 | 2 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0013t0012 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0018t0001 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0019t0001 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0020t0003 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0021t0003 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0022t0001 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0023t0003 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0030t0002 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0032t0002 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0001c0035t0007 | 0/0 | 5323 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5318): Show |
chr12 | 131889622 | 131928150 |
a0002c0004t0002 | 0/0 | 5322 | 2 | 0 | 0 | 0 | 2 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0004t0003 | 0/0 | 5322 | 2 | 1 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0004t0004 | 0/0 | 5322 | 23 | 5 | 10 | 2 | 0 | 6 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0004t0022 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0004t0023 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0008t0004 | 0/0 | 5322 | 7 | 4 | 3 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0008t0025 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0011t0004 | 0/0 | 5322 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0025t0001 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0031t0002 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0002c0033t0002 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0003c0014t0001 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0003c0027t0001 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0004c0016t0013 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0005c0034t0004 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0006c0036t0004 | 0/0 | 5322 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0007c0015t0001 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0008c0026t0001 | 0/0 | 5322 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0009c0024t0003 | 0/0 | 5322 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0010c0028t0002 | 0/0 | 5322 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
a0011c0037t0003 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5350): Show |
chr12 | 131889622 | 131928150 |
a0012c0017t0001 | 0/0 | 5304 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5299): Show |
chr12 | 131889622 | 131928150 |
a0013c0029t0027 | 0/1 | 5322 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | AGTGC others(5317): Show |
chr12 | 131889622 | 131928150 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 3 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0015g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0017g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0020g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0021g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0001t0026g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0011g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0002t0019g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0009g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0010g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0014g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0014g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0016g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0003t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0005t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0006t0028g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0007t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0009t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0009t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0009t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0009t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0009t0005g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0010t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0010t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0010t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0010t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0012t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0012t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0013t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0018t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0019t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0020t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0021t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0022t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0023t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0030t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0032t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0001c0035t0007g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0022g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0004t0023g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0008t0025g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0011t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0011t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0011t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0025t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0031t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0002c0033t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0003c0014t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0003c0027t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0004c0016t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0005c0034t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0006c0036t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0007c0015t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0008c0026t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0009c0024t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0010c0028t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0011c0037t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0012c0017t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
a0013c0029t0027g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | GBR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0167 | EUR | GBR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00140 | hp1 | a0002 | c0004 | t0002 | g0172 | EUR | GBR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00140 | hp2 | a0001 | c0006 | t0004 | g0188 | EUR | GBR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0119 | EUR | FIN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | FIN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00408 | hp1 | a0001 | c0003 | t0008 | g0242 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00438 | hp2 | a0001 | c0003 | t0003 | g0281 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00558 | hp1 | a0001 | c0003 | t0003 | g0241 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00558 | hp2 | a0001 | c0003 | t0003 | g0236 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00597 | hp1 | a0001 | c0003 | t0002 | g0244 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00597 | hp2 | a0004 | c0016 | t0013 | g0073 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00609 | hp1 | a0001 | c0003 | t0003 | g0292 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0316 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00733 | hp2 | a0002 | c0008 | t0004 | g0215 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG00735 | hp2 | a0002 | c0008 | t0004 | g0025 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01071 | hp1 | a0001 | c0006 | t0028 | g0184 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01071 | hp2 | a0001 | c0010 | t0002 | g0209 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01074 | hp1 | a0002 | c0004 | t0004 | g0012 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01074 | hp2 | a0001 | c0006 | t0004 | g0276 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01081 | hp1 | a0001 | c0019 | t0001 | g0081 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01081 | hp2 | a0002 | c0004 | t0004 | g0012 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01106 | hp2 | a0001 | c0010 | t0002 | g0218 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01109 | hp1 | a0002 | c0031 | t0002 | g0198 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01109 | hp2 | a0001 | c0020 | t0003 | g0251 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01167 | hp2 | a0001 | c0007 | t0001 | g0007 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01168 | hp2 | a0002 | c0008 | t0025 | g0154 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01169 | hp1 | a0001 | c0007 | t0001 | g0007 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0317 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01192 | hp1 | a0001 | c0006 | t0004 | g0210 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01243 | hp1 | a0002 | c0004 | t0004 | g0212 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01255 | hp1 | a0001 | c0005 | t0001 | g0204 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01255 | hp2 | a0002 | c0008 | t0004 | g0029 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01256 | hp1 | a0002 | c0004 | t0004 | g0030 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01256 | hp2 | a0001 | c0006 | t0004 | g0186 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01261 | hp1 | a0001 | c0002 | t0011 | g0038 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01261 | hp2 | a0001 | c0006 | t0003 | g0169 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01346 | hp1 | a0005 | c0034 | t0004 | g0211 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01346 | hp2 | a0002 | c0004 | t0004 | g0013 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01358 | hp1 | a0002 | c0004 | t0004 | g0013 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01358 | hp2 | a0001 | c0003 | t0003 | g0232 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01433 | hp2 | a0002 | c0004 | t0004 | g0214 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0200 | EUR | IBS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01515 | hp2 | a0006 | c0036 | t0004 | g0202 | EUR | IBS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01516 | hp1 | a0002 | c0033 | t0002 | g0216 | EUR | IBS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01516 | hp2 | a0001 | c0023 | t0003 | g0234 | EUR | IBS | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01884 | hp1 | a0001 | c0002 | t0004 | g0082 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01884 | hp2 | a0001 | c0003 | t0003 | g0015 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01891 | hp2 | a0007 | c0015 | t0001 | g0219 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01928 | hp2 | a0001 | c0003 | t0003 | g0226 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01952 | hp1 | a0001 | c0003 | t0003 | g0262 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0146 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01978 | hp1 | a0002 | c0004 | t0003 | g0180 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01981 | hp1 | a0001 | c0003 | t0003 | g0260 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01981 | hp2 | a0001 | c0030 | t0002 | g0199 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01993 | hp1 | a0002 | c0004 | t0004 | g0213 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02004 | hp1 | a0001 | c0003 | t0003 | g0249 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02004 | hp2 | a0001 | c0005 | t0001 | g0173 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02027 | hp1 | a0001 | c0003 | t0003 | g0258 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02027 | hp2 | a0002 | c0004 | t0004 | g0141 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02040 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0282 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02055 | hp1 | a0002 | c0004 | t0004 | g0019 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02056 | hp1 | a0001 | c0009 | t0005 | g0113 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0294 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02083 | hp2 | a0001 | c0002 | t0013 | g0074 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02165 | hp1 | a0001 | c0003 | t0003 | g0285 | EAS | CDX | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02165 | hp2 | a0001 | c0001 | t0021 | g0132 | EAS | CDX | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02257 | hp1 | a0001 | c0032 | t0002 | g0028 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02257 | hp2 | a0002 | c0004 | t0004 | g0020 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02258 | hp2 | a0001 | c0003 | t0002 | g0313 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02273 | hp1 | a0008 | c0026 | t0001 | g0099 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02293 | hp1 | a0002 | c0004 | t0004 | g0133 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02293 | hp2 | a0001 | c0005 | t0001 | g0138 | AMR | PEL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02523 | hp1 | a0001 | c0001 | t0020 | g0175 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02523 | hp2 | a0001 | c0003 | t0006 | g0238 | EAS | KHV | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02572 | hp2 | a0002 | c0004 | t0004 | g0136 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02622 | hp1 | a0001 | c0002 | t0003 | g0089 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02647 | hp1 | a0001 | c0021 | t0003 | g0309 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02723 | hp1 | a0003 | c0027 | t0001 | g0109 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02735 | hp1 | a0001 | c0009 | t0005 | g0018 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02735 | hp2 | a0001 | c0006 | t0004 | g0268 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02738 | hp1 | a0001 | c0001 | t0015 | g0191 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02738 | hp2 | a0001 | c0001 | t0017 | g0143 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02895 | hp1 | a0002 | c0008 | t0004 | g0130 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02897 | hp1 | a0002 | c0008 | t0004 | g0131 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02922 | hp1 | a0001 | c0003 | t0003 | g0259 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02965 | hp1 | a0001 | c0007 | t0001 | g0006 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02965 | hp2 | a0002 | c0004 | t0004 | g0022 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02970 | hp2 | a0001 | c0013 | t0012 | g0303 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02976 | hp1 | a0001 | c0007 | t0001 | g0006 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03017 | hp1 | a0001 | c0010 | t0002 | g0207 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03017 | hp2 | a0002 | c0004 | t0022 | g0153 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03041 | hp1 | a0001 | c0002 | t0019 | g0049 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0315 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0054 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03130 | hp2 | a0001 | c0003 | t0018 | g0247 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03139 | hp1 | a0002 | c0008 | t0004 | g0135 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0091 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0312 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0304 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03209 | hp2 | a0002 | c0008 | t0004 | g0183 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03239 | hp1 | a0002 | c0004 | t0004 | g0177 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03453 | hp1 | a0001 | c0022 | t0001 | g0087 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03490 | hp1 | a0001 | c0003 | t0010 | g0231 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03491 | hp2 | a0001 | c0003 | t0003 | g0014 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03492 | hp1 | a0001 | c0003 | t0010 | g0253 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0014 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03516 | hp2 | a0001 | c0007 | t0011 | g0051 | AFR | ESN | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03540 | hp1 | a0001 | c0007 | t0001 | g0055 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0096 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0056 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03654 | hp1 | a0002 | c0004 | t0004 | g0179 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03654 | hp2 | a0001 | c0009 | t0005 | g0121 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03688 | hp2 | a0001 | c0010 | t0004 | g0208 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03704 | hp1 | a0001 | c0035 | t0007 | g0004 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03704 | hp2 | a0002 | c0004 | t0004 | g0023 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03710 | hp2 | a0001 | c0006 | t0002 | g0277 | SAS | PJL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03831 | hp1 | a0001 | c0003 | t0003 | g0290 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03831 | hp2 | a0001 | c0003 | t0003 | g0246 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03927 | hp1 | a0002 | c0004 | t0004 | g0017 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0150 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03942 | hp1 | a0001 | c0001 | t0007 | g0159 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0255 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0040 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04115 | hp2 | a0002 | c0004 | t0023 | g0145 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04184 | hp1 | a0002 | c0004 | t0004 | g0157 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | BEB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04199 | hp1 | a0002 | c0004 | t0004 | g0269 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04204 | hp1 | a0002 | c0025 | t0001 | g0080 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG04204 | hp2 | a0001 | c0006 | t0004 | g0181 | SAS | STU | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18522 | hp1 | a0001 | c0003 | t0012 | g0302 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18747 | hp1 | a0001 | c0003 | t0003 | g0278 | EAS | CHB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | CHB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18940 | hp2 | a0001 | c0003 | t0003 | g0257 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18943 | hp1 | a0001 | c0003 | t0024 | g0283 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18943 | hp2 | a0001 | c0005 | t0001 | g0174 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18945 | hp1 | a0001 | c0003 | t0008 | g0254 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18945 | hp2 | a0001 | c0005 | t0002 | g0170 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18946 | hp1 | a0001 | c0005 | t0001 | g0203 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18947 | hp1 | a0001 | c0003 | t0003 | g0240 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18947 | hp2 | a0001 | c0003 | t0009 | g0005 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18948 | hp1 | a0002 | c0011 | t0004 | g0024 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18950 | hp1 | a0001 | c0003 | t0003 | g0256 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18952 | hp1 | a0001 | c0009 | t0005 | g0120 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18952 | hp2 | a0001 | c0003 | t0003 | g0284 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18959 | hp1 | a0002 | c0004 | t0004 | g0185 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18959 | hp2 | a0001 | c0003 | t0003 | g0229 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18964 | hp1 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18964 | hp2 | a0001 | c0003 | t0014 | g0264 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18966 | hp1 | a0001 | c0003 | t0003 | g0252 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18967 | hp1 | a0001 | c0003 | t0014 | g0233 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18969 | hp1 | a0001 | c0003 | t0003 | g0265 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18969 | hp2 | a0001 | c0003 | t0003 | g0250 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18970 | hp2 | a0001 | c0012 | t0001 | g0077 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18971 | hp1 | a0001 | c0003 | t0003 | g0266 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18971 | hp2 | a0001 | c0005 | t0001 | g0192 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18973 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18975 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18975 | hp2 | a0001 | c0003 | t0006 | g0222 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18980 | hp1 | a0002 | c0011 | t0004 | g0027 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18980 | hp2 | a0001 | c0005 | t0002 | g0156 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18981 | hp1 | a0001 | c0005 | t0001 | g0301 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18982 | hp1 | a0001 | c0003 | t0009 | g0005 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18983 | hp1 | a0001 | c0003 | t0003 | g0261 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18983 | hp2 | a0001 | c0003 | t0009 | g0005 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18991 | hp1 | a0001 | c0018 | t0001 | g0034 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18991 | hp2 | a0001 | c0003 | t0006 | g0267 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18998 | hp1 | a0002 | c0011 | t0004 | g0026 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA18998 | hp2 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19000 | hp1 | a0001 | c0005 | t0001 | g0151 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19000 | hp2 | a0001 | c0003 | t0003 | g0239 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19004 | hp2 | a0009 | c0024 | t0003 | g0289 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19005 | hp1 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19007 | hp1 | a0001 | c0003 | t0003 | g0288 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19007 | hp2 | a0001 | c0012 | t0001 | g0076 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0230 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0248 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19012 | hp1 | a0001 | c0003 | t0003 | g0223 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19030 | hp2 | a0010 | c0028 | t0002 | g0308 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0311 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0093 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19056 | hp1 | a0001 | c0003 | t0008 | g0225 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19056 | hp2 | a0001 | c0005 | t0001 | g0158 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19060 | hp2 | a0011 | c0037 | t0003 | g0280 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19062 | hp1 | a0001 | c0003 | t0016 | g0279 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19063 | hp1 | a0001 | c0003 | t0003 | g0263 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19063 | hp2 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19064 | hp2 | a0001 | c0005 | t0001 | g0152 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19066 | hp1 | a0001 | c0003 | t0003 | g0287 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19080 | hp1 | a0001 | c0001 | t0026 | g0297 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19080 | hp2 | a0001 | c0009 | t0005 | g0118 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0237 | EAS | JPT | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19240 | hp1 | a0002 | c0004 | t0004 | g0021 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0059 | AFR | YRI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ASW | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ASW | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20752 | hp1 | a0002 | c0004 | t0002 | g0155 | EUR | TSI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20805 | hp1 | a0001 | c0003 | t0003 | g0015 | EUR | TSI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | TSI | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20905 | hp1 | a0001 | c0006 | t0004 | g0149 | SAS | GIH | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | GIH | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG01123 | hp2 | a0002 | c0004 | t0004 | g0031 | AMR | CLM | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02559 | hp1 | a0003 | c0014 | t0001 | g0310 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0314 | AFR | ACB | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0305 | AFR | MSL | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG06807 | hp1 | a0001 | c0007 | t0001 | g0052 | AFR | USA | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
HG06807 | hp2 | a0002 | c0004 | t0003 | g0171 | AFR | USA | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20300 | hp1 | a0001 | c0005 | t0001 | g0322 | AFR | USA | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA20300 | hp2 | a0001 | c0003 | t0003 | g0245 | AFR | USA | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
NA21309 | hp2 | a0012 | c0017 | t0001 | g0112 | AFR | LWK | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
homoSapiens | chm13v2 | a0013 | c0029 | t0027 | g0217 | REF | REF | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0220 | REF | REF | ULK1_chr12_131889622_131928150 | ULK1 | chr12 | 131889622 | 131928150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131909143 | A | AGGTCATC others(26): Show |
1 | a0011 | 1 | NA19060.hp2 | disruptive_inframe_insertion | MODERATE | c.575_607dupTCATCATG others(25): Show |
p.Val192_Ala202dup | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/28 | 988/5322 | 608/3153 | 203/1050 | INFO_REALIGN_3_PRIME | chr12 | 131909143 | ||
chr12:131909833 | C | T | 1 | a0006 | 1 | HG01515.hp2 | missense_variant&splice_region_variant | MODERATE | c.725C>T | p.Thr242Ile | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 9/28 | 1105/5322 | 725/3153 | 242/1050 | chr12 | 131909833 | |||
chr12:131913818 | G | A | 1 | a0004 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1229G>A | p.Ser410Asn | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/28 | 1609/5322 | 1229/3153 | 410/1050 | chr12 | 131913818 | |||
chr12:131914459 | C | G | 1 | a0005 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.1355C>G | p.Thr452Ser | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/28 | 1735/5322 | 1355/3153 | 452/1050 | chr12 | 131914459 | |||
chr12:131915112 | C | T | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1403C>T | p.Thr468Ile | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 17/28 | 1783/5322 | 1403/3153 | 468/1050 | chr12 | 131915112 | |||
chr12:131916078 | CCGGAACC others(11): Show |
C | 1 | a0012 | 1 | NA21309.hp2 | disruptive_inframe_deletion | MODERATE | c.1799_1816delGGAACC others(12): Show |
p.Arg600_Ser605del | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/28 | 2179/5322 | 1799/3153 | 600/1050 | INFO_REALIGN_3_PRIME | chr12 | 131916078 | ||
chr12:131916557 | C | T | 1 | a0003 | 2 | HG02559.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.2038C>T | p.Arg680Trp | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/28 | 2418/5322 | 2038/3153 | 680/1050 | chr12 | 131916557 | |||
chr12:131916994 | C | T | 1 | a0008 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.2114C>T | p.Ala705Val | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/28 | 2494/5322 | 2114/3153 | 705/1050 | chr12 | 131916994 | |||
chr12:131917012 | C | T | 1 | a0007 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2132C>T | p.Ala711Val | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/28 | 2512/5322 | 2132/3153 | 711/1050 | chr12 | 131917012 | |||
chr12:131917021 | C | T | 3 | a0002 a0005 a0006 |
45 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(42): Show |
missense_variant | MODERATE | c.2141C>T | p.Pro714Leu | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/28 | 2521/5322 | 2141/3153 | 714/1050 | chr12 | 131917021 | |||
chr12:131921220 | G | A | 1 | a0009 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.3082G>A | p.Glu1028Lys | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 27/28 | 3462/5322 | 3082/3153 | 1028/1050 | chr12 | 131921220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131909219 | G | A | 3 | a0001c0013 a0003c0014 a0007c0015 |
3 | HG01891.hp2 HG02559.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.648G>A | p.Thr216Thr | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/28 | 1028/5322 | 648/3153 | 216/1050 | chr12 | 131909219 | |||
chr12:131912058 | C | T | 15 | a0001c0001 a0001c0005 a0001c0006 others(12): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
synonymous_variant | LOW | c.1065C>T | p.Asp355Asp | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/28 | 1445/5322 | 1065/3153 | 355/1050 | chr12 | 131912058 | |||
chr12:131913825 | C | G | 1 | a0001c0035 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1236C>G | p.Pro412Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/28 | 1616/5322 | 1236/3153 | 412/1050 | chr12 | 131913825 | |||
chr12:131916003 | C | G | 1 | a0002c0033 | 1 | HG01516.hp1 | synonymous_variant | LOW | c.1722C>G | p.Pro574Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/28 | 2102/5322 | 1722/3153 | 574/1050 | chr12 | 131916003 | |||
chr12:131916069 | G | A | 1 | a0001c0007 | 8 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(5): Show |
synonymous_variant | LOW | c.1788G>A | p.Leu596Leu | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/28 | 2168/5322 | 1788/3153 | 596/1050 | chr12 | 131916069 | |||
chr12:131916108 | C | T | 2 | a0001c0005 a0001c0032 |
15 | HG01255.hp1 HG01975.hp1 HG02004.hp2 others(12): Show |
synonymous_variant | LOW | c.1827C>T | p.Pro609Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/28 | 2207/5322 | 1827/3153 | 609/1050 | chr12 | 131916108 | |||
chr12:131916505 | C | T | 3 | a0001c0010 a0001c0030 a0002c0031 |
6 | HG01071.hp2 HG01106.hp2 HG01109.hp1 others(3): Show |
synonymous_variant | LOW | c.1986C>T | p.Pro662Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/28 | 2366/5322 | 1986/3153 | 662/1050 | chr12 | 131916505 | |||
chr12:131917052 | C | A | 1 | a0001c0018 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.2172C>A | p.Pro724Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/28 | 2552/5322 | 2172/3153 | 724/1050 | chr12 | 131917052 | |||
chr12:131917475 | T | C | 25 | a0001c0001 a0001c0002 a0001c0005 others(22): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
synonymous_variant | LOW | c.2247T>C | p.Pro749Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/28 | 2627/5322 | 2247/3153 | 749/1050 | chr12 | 131917475 | |||
chr12:131917481 | G | A | 4 | a0001c0010 a0001c0019 a0001c0023 others(1): Show |
7 | HG01071.hp2 HG01081.hp1 HG01106.hp2 others(4): Show |
synonymous_variant | LOW | c.2253G>A | p.Pro751Pro | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/28 | 2633/5322 | 2253/3153 | 751/1050 | chr12 | 131917481 | |||
chr12:131917499 | C | A | 1 | a0001c0020 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.2271C>A | p.Gly757Gly | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/28 | 2651/5322 | 2271/3153 | 757/1050 | chr12 | 131917499 | |||
chr12:131919268 | C | T | 1 | a0001c0012 | 2 | NA18970.hp2 NA19007.hp2 |
synonymous_variant | LOW | c.2568C>T | p.His856His | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 24/28 | 2948/5322 | 2568/3153 | 856/1050 | chr12 | 131919268 | |||
chr12:131919556 | C | T | 1 | a0001c0022 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.2769C>T | p.Ala923Ala | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/28 | 3149/5322 | 2769/3153 | 923/1050 | chr12 | 131919556 | |||
chr12:131919565 | C | T | 2 | a0001c0021 a0010c0028 |
2 | HG02647.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.2778C>T | p.Leu926Leu | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/28 | 3158/5322 | 2778/3153 | 926/1050 | chr12 | 131919565 | |||
chr12:131920046 | G | A | 2 | a0001c0021 a0010c0028 |
2 | HG02647.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.2871G>A | p.Leu957Leu | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/28 | 3251/5322 | 2871/3153 | 957/1050 | chr12 | 131920046 | |||
chr12:131921334 | G | A | 1 | a0001c0009 | 5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
synonymous_variant | LOW | c.3126G>A | p.Ser1042Ser | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 3506/5322 | 3126/3153 | 1042/1050 | chr12 | 131921334 | |||
chr12:131921337 | G | A | 1 | a0002c0011 | 3 | NA18948.hp1 NA18980.hp1 NA18998.hp1 |
synonymous_variant | LOW | c.3129G>A | p.Ala1043Ala | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 3509/5322 | 3129/3153 | 1043/1050 | chr12 | 131921337 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131894695 | G | T | 1 | a0001c0003t0014 | 2 | NA18964.hp2 NA18967.hp1 |
5_prime_UTR_variant | MODIFIER | c.-307G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 307 | chr12 | 131894695 | ||||||
chr12:131894758 | C | G | 1 | a0001c0003t0009 | 3 | NA18947.hp2 NA18982.hp1 NA18983.hp2 |
5_prime_UTR_variant | MODIFIER | c.-244C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 244 | chr12 | 131894758 | ||||||
chr12:131894821 | G | A | 1 | a0001c0003t0010 | 2 | HG03490.hp1 HG03492.hp1 |
5_prime_UTR_variant | MODIFIER | c.-181G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 181 | chr12 | 131894821 | ||||||
chr12:131894828 | G | A | 1 | a0001c0001t0015 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-174G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 174 | chr12 | 131894828 | ||||||
chr12:131894893 | G | T | 2 | a0001c0002t0013 a0004c0016t0013 |
2 | HG00597.hp2 HG02083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-109G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 109 | chr12 | 131894893 | ||||||
chr12:131894968 | A | AC | 6 | a0001c0001t0007 a0001c0001t0017 a0001c0002t0011 others(3): Show |
9 | HG01261.hp1 HG02523.hp2 HG02738.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-28dupC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 27 | INFO_REALIGN_3_PRIME | chr12 | 131894968 | |||||
chr12:131894975 | G | C | 1 | a0001c0003t0016 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-27G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/28 | 27 | chr12 | 131894975 | ||||||
chr12:131921436 | G | A | 1 | a0001c0003t0008 | 3 | HG00408.hp1 NA18945.hp1 NA19056.hp1 |
3_prime_UTR_variant | MODIFIER | c.*75G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 75 | chr12 | 131921436 | ||||||
chr12:131921452 | G | A | 1 | a0001c0003t0018 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*91G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 91 | chr12 | 131921452 | ||||||
chr12:131921522 | C | T | 1 | a0001c0006t0028 | 1 | HG01071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 161 | chr12 | 131921522 | ||||||
chr12:131921617 | C | G | 1 | a0001c0009t0005 | 5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 256 | chr12 | 131921617 | ||||||
chr12:131921972 | C | T | 1 | a0001c0001t0026 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 611 | chr12 | 131921972 | ||||||
chr12:131921980 | C | T | 1 | a0001c0001t0017 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 619 | chr12 | 131921980 | ||||||
chr12:131922121 | G | C | 22 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0020 others(19): Show |
129 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 760 | chr12 | 131922121 | ||||||
chr12:131922270 | G | T | 2 | a0001c0003t0012 a0001c0013t0012 |
2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*909G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 909 | chr12 | 131922270 | ||||||
chr12:131922272 | G | A | 1 | a0001c0001t0021 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*911G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 911 | chr12 | 131922272 | ||||||
chr12:131922278 | G | C | 2 | a0001c0003t0012 a0001c0013t0012 |
2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*917G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 917 | chr12 | 131922278 | ||||||
chr12:131922463 | T | C | 11 | a0001c0002t0004 a0001c0002t0019 a0001c0006t0004 others(8): Show |
47 | HG00140.hp2 HG00733.hp2 HG00735.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1102T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1102 | chr12 | 131922463 | ||||||
chr12:131922482 | G | C | 1 | a0002c0004t0022 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1121G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1121 | chr12 | 131922482 | ||||||
chr12:131922544 | A | G | 54 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(51): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*1183A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1183 | chr12 | 131922544 | ||||||
chr12:131922661 | A | C | 1 | a0001c0001t0020 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1300A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1300 | chr12 | 131922661 | ||||||
chr12:131922709 | G | A | 2 | a0001c0002t0002 a0001c0003t0002 |
10 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1348G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1348 | chr12 | 131922709 | ||||||
chr12:131922823 | G | A | 1 | a0002c0008t0025 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1462 | chr12 | 131922823 | ||||||
chr12:131923008 | C | A | 1 | a0001c0003t0024 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1647C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1647 | chr12 | 131923008 | ||||||
chr12:131923074 | C | T | 2 | a0001c0003t0012 a0001c0013t0012 |
2 | HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1713C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1713 | chr12 | 131923074 | ||||||
chr12:131923114 | T | G | 1 | a0002c0004t0023 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1753T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 28/28 | 1753 | chr12 | 131923114 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:131895196 | G | A | 1 | a0002c0004t0004g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.111+84G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895196 | |||||||
chr12:131895225 | C | T | 1 | a0001c0005t0001g0322 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.111+113C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895225 | |||||||
chr12:131895334 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(10): Show |
17 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.111+222A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895334 | |||||||
chr12:131895370 | G | A | 1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.112-231G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895370 | |||||||
chr12:131895434 | C | G | 1 | a0003c0014t0001g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112-167C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895434 | |||||||
chr12:131895477 | C | A | 9 | a0002c0004t0004g0019 a0002c0004t0004g0020 a0002c0004t0004g0021 others(6): Show |
9 | HG00735.hp2 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.112-124C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895477 | |||||||
chr12:131895484 | T | G | 1 | a0001c0032t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112-117T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895484 | |||||||
chr12:131895507 | G | A | 1 | a0002c0008t0004g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.112-94G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 1/27 | chr12 | 131895507 | |||||||
chr12:131895877 | C | T | 8 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(5): Show |
8 | HG01891.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+53C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131895877 | |||||||
chr12:131895977 | T | G | 101 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(98): Show |
106 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.246+153T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131895977 | |||||||
chr12:131896219 | C | T | 6 | a0001c0001t0002g0296 a0001c0001t0002g0298 a0001c0001t0002g0299 others(3): Show |
6 | NA18977.hp1 NA18981.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+395C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896219 | |||||||
chr12:131896250 | C | G | 1 | a0001c0003t0003g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.246+426C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896250 | |||||||
chr12:131896277 | CA | C | 18 | a0001c0003t0003g0278 a0001c0003t0003g0281 a0001c0003t0003g0282 others(15): Show |
18 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+454delA | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896277 | |||||||
chr12:131896278 | A | G | 57 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(54): Show |
61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.246+454A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896278 | |||||||
chr12:131896282 | C | G | 18 | a0001c0003t0003g0278 a0001c0003t0003g0281 a0001c0003t0003g0282 others(15): Show |
18 | HG00438.hp2 HG00609.hp1 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+458C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896282 | |||||||
chr12:131896500 | G | A | 4 | a0002c0004t0004g0019 a0002c0004t0004g0020 a0002c0004t0004g0021 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+676G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896500 | |||||||
chr12:131896623 | G | T | 1 | a0001c0006t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.246+799G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896623 | |||||||
chr12:131896648 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.246+824G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896648 | |||||||
chr12:131896878 | G | A | 7 | a0001c0002t0002g0311 a0001c0002t0002g0316 a0001c0002t0002g0317 others(4): Show |
7 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+1054G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896878 | |||||||
chr12:131896999 | C | T | 1 | a0001c0006t0004g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.246+1175C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131896999 | |||||||
chr12:131897014 | C | T | 14 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(11): Show |
14 | HG00280.hp1 HG01928.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+1190C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897014 | |||||||
chr12:131897017 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
5 | HG01934.hp2 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+1193G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897017 | |||||||
chr12:131897149 | G | A | 2 | a0002c0008t0004g0130 a0002c0008t0004g0131 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.246+1325G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897149 | |||||||
chr12:131897151 | C | T | 75 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(72): Show |
79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.246+1327C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897151 | |||||||
chr12:131897305 | A | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0318 a0001c0001t0001g0319 others(2): Show |
8 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+1481A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897305 | |||||||
chr12:131897313 | T | G | 1 | a0001c0001t0021g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+1489T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897313 | |||||||
chr12:131897375 | T | C | 123 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(120): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.246+1551T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897375 | |||||||
chr12:131897379 | C | T | 1 | a0001c0010t0002g0218 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.246+1555C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897379 | |||||||
chr12:131897456 | A | G | 85 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(82): Show |
90 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.246+1632A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897456 | |||||||
chr12:131897683 | T | G | 1 | a0001c0003t0006g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.246+1859T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897683 | |||||||
chr12:131897753 | GAA | G | 8 | a0001c0006t0004g0210 a0002c0004t0004g0013 a0002c0004t0004g0212 others(5): Show |
9 | HG00733.hp2 HG01192.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+1936_246+1937d others(4): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131897753 | ||||||
chr12:131897767 | C | T | 1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.246+1943C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897767 | |||||||
chr12:131897847 | C | T | 3 | a0001c0010t0002g0207 a0001c0010t0002g0209 a0001c0010t0004g0208 |
3 | HG01071.hp2 HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.246+2023C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131897847 | |||||||
chr12:131897859 | A | AC | 4 | a0001c0002t0001g0032 a0001c0003t0003g0223 a0001c0021t0003g0309 others(1): Show |
4 | HG01106.hp1 HG02055.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2037dupC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131897859 | ||||||
chr12:131898135 | G | A | 1 | a0001c0006t0004g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.246+2311G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898135 | |||||||
chr12:131898368 | G | A | 1 | a0001c0003t0003g0278 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+2544G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898368 | |||||||
chr12:131898587 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.246+2763C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898587 | |||||||
chr12:131898602 | A | G | 1 | a0002c0004t0004g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.246+2778A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898602 | |||||||
chr12:131898692 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(10): Show |
17 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.246+2868C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898692 | |||||||
chr12:131898830 | C | A | 320 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.246+3006C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898830 | |||||||
chr12:131898920 | C | T | 1 | a0012c0017t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.246+3096C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131898920 | |||||||
chr12:131899081 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(192): Show |
208 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.246+3257A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899081 | |||||||
chr12:131899275 | G | A | 1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.246+3451G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899275 | |||||||
chr12:131899282 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(10): Show |
17 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.246+3458G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899282 | |||||||
chr12:131899331 | G | C | 2 | a0002c0008t0004g0130 a0002c0008t0004g0131 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.246+3507G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899331 | |||||||
chr12:131899412 | T | G | 1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.246+3588T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899412 | |||||||
chr12:131899556 | TC | T | 14 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(11): Show |
14 | HG00280.hp1 HG01928.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.246+3733delC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899556 | |||||||
chr12:131899557 | C | T | 75 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(72): Show |
79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.246+3733C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899557 | |||||||
chr12:131899572 | C | A | 1 | a0001c0001t0001g0318 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.246+3748C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899572 | |||||||
chr12:131899797 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.246+3973G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899797 | |||||||
chr12:131899834 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.246+4010T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899834 | |||||||
chr12:131899857 | C | A | 1 | a0001c0001t0002g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.246+4033C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899857 | |||||||
chr12:131899890 | C | T | 85 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(82): Show |
90 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.246+4066C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899890 | |||||||
chr12:131899934 | A | G | 2 | a0001c0001t0007g0205 a0010c0028t0002g0308 |
2 | NA18977.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.246+4110A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131899934 | |||||||
chr12:131900016 | C | T | 2 | a0001c0002t0002g0316 a0001c0002t0002g0317 |
2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.246+4192C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900016 | |||||||
chr12:131900032 | G | A | 1 | a0001c0009t0005g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.246+4208G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900032 | |||||||
chr12:131900074 | G | A | 1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.246+4250G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900074 | |||||||
chr12:131900114 | CA | C | 29 | a0001c0001t0001g0320 a0001c0001t0002g0137 a0001c0001t0002g0139 others(26): Show |
29 | HG00280.hp2 HG00733.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.246+4314delA | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131900114 | ||||||
chr12:131900114 | CAA | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(194): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.246+4313_246+4314d others(4): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131900114 | ||||||
chr12:131900114 | CAAA | C | 72 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(69): Show |
76 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.246+4312_246+4314d others(5): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131900114 | ||||||
chr12:131900286 | C | T | 125 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(122): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.246+4462C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900286 | |||||||
chr12:131900289 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.246+4465G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900289 | |||||||
chr12:131900381 | G | T | 75 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(72): Show |
79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.246+4557G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900381 | |||||||
chr12:131900440 | A | G | 8 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(5): Show |
8 | HG01891.hp1 HG02647.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+4616A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900440 | |||||||
chr12:131900453 | C | T | 1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.246+4629C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900453 | |||||||
chr12:131900476 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0002g0200 |
2 | HG01515.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.246+4652C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900476 | |||||||
chr12:131900535 | G | A | 76 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(73): Show |
80 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.246+4711G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900535 | |||||||
chr12:131900637 | G | GC | 74 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(71): Show |
78 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.246+4819dupC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131900637 | ||||||
chr12:131900805 | C | G | 3 | a0001c0002t0002g0304 a0001c0003t0012g0302 a0001c0013t0012g0303 |
3 | HG02970.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+4981C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900805 | |||||||
chr12:131900894 | C | T | 84 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(81): Show |
89 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.246+5070C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900894 | |||||||
chr12:131900895 | G | C | 3 | a0002c0004t0004g0136 a0002c0008t0004g0130 a0002c0008t0004g0131 |
3 | HG02572.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.246+5071G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131900895 | |||||||
chr12:131901025 | G | A | 3 | a0001c0002t0002g0304 a0001c0003t0012g0302 a0001c0013t0012g0303 |
3 | HG02970.hp2 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.246+5201G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901025 | |||||||
chr12:131901039 | C | CTTT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(11): Show |
18 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.246+5228_246+5230d others(5): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131901039 | ||||||
chr12:131901039 | CT | C | 8 | a0001c0001t0002g0114 a0001c0002t0001g0044 a0001c0002t0001g0045 others(5): Show |
8 | HG01516.hp1 HG01516.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.246+5230delT | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131901039 | ||||||
chr12:131901282 | C | T | 1 | a0001c0003t0003g0275 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.246+5458C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901282 | |||||||
chr12:131901355 | CAAAAAAA | C | 14 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(11): Show |
14 | HG00280.hp1 HG01928.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.247-5529_247-5523d others(9): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 131901355 | ||||||
chr12:131901359 | A | C | 1 | a0001c0001t0021g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.247-5533A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901359 | |||||||
chr12:131901370 | G | A | 1 | a0001c0003t0003g0226 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.247-5522G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901370 | |||||||
chr12:131901371 | A | G | 1 | a0001c0003t0003g0226 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.247-5521A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901371 | |||||||
chr12:131901374 | A | C | 83 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(80): Show |
88 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(85): Show |
intron_variant | MODIFIER | c.247-5518A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901374 | |||||||
chr12:131901505 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.247-5387G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901505 | |||||||
chr12:131901737 | G | A | 3 | a0001c0002t0001g0048 a0001c0002t0001g0050 a0001c0002t0019g0049 |
3 | HG01934.hp1 HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.247-5155G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901737 | |||||||
chr12:131901800 | G | A | 1 | a0010c0028t0002g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247-5092G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901800 | |||||||
chr12:131901853 | C | T | 6 | a0001c0010t0002g0207 a0001c0010t0002g0209 a0001c0010t0002g0218 others(3): Show |
6 | HG01071.hp2 HG01106.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-5039C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901853 | |||||||
chr12:131901854 | G | A | 84 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(81): Show |
89 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.247-5038G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901854 | |||||||
chr12:131901856 | C | G | 1 | a0001c0032t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.247-5036C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131901856 | |||||||
chr12:131902103 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247-4789G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902103 | |||||||
chr12:131902162 | C | T | 1 | a0002c0004t0023g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.247-4730C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902162 | |||||||
chr12:131902458 | G | C | 2 | a0003c0014t0001g0310 a0007c0015t0001g0219 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.247-4434G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902458 | |||||||
chr12:131902464 | G | T | 1 | a0012c0017t0001g0112 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247-4428G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902464 | |||||||
chr12:131902630 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | NA18966.hp2 NA18995.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.247-4262C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902630 | |||||||
chr12:131902684 | T | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(83): Show |
91 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.247-4208T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902684 | |||||||
chr12:131902841 | C | G | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0021g0132 |
3 | HG00408.hp2 HG02165.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.247-4051C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902841 | |||||||
chr12:131902907 | G | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(1): Show |
4 | NA18957.hp1 NA18963.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-3985G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131902907 | |||||||
chr12:131903013 | C | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(83): Show |
91 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(88): Show |
intron_variant | MODIFIER | c.247-3879C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903013 | |||||||
chr12:131903110 | T | C | 1 | a0001c0006t0004g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.247-3782T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903110 | |||||||
chr12:131903147 | C | T | 2 | a0002c0004t0004g0030 a0002c0004t0004g0031 |
2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.247-3745C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903147 | |||||||
chr12:131903167 | C | T | 5 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(2): Show |
5 | NA18944.hp2 NA18946.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3725C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903167 | |||||||
chr12:131903298 | G | A | 1 | a0001c0003t0003g0236 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.247-3594G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903298 | |||||||
chr12:131903353 | C | G | 5 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(2): Show |
5 | HG01891.hp1 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-3539C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903353 | |||||||
chr12:131903432 | G | T | 1 | a0001c0003t0006g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.247-3460G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903432 | |||||||
chr12:131903510 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.247-3382C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903510 | |||||||
chr12:131903527 | C | G | 1 | a0001c0002t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.247-3365C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903527 | |||||||
chr12:131903940 | G | A | 1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247-2952G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903940 | |||||||
chr12:131903955 | C | T | 69 | a0001c0002t0001g0243 a0001c0003t0002g0244 a0001c0003t0003g0014 others(66): Show |
73 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.247-2937C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903955 | |||||||
chr12:131903999 | G | T | 130 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(127): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.247-2893G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131903999 | |||||||
chr12:131904019 | C | A | 1 | a0001c0001t0002g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.247-2873C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904019 | |||||||
chr12:131904033 | A | C | 1 | a0001c0002t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247-2859A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904033 | |||||||
chr12:131904327 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.247-2565T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904327 | |||||||
chr12:131904424 | G | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(3): Show |
10 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-2468G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904424 | |||||||
chr12:131904443 | C | T | 74 | a0001c0002t0001g0008 a0001c0002t0001g0032 a0001c0002t0001g0035 others(71): Show |
75 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.247-2449C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904443 | |||||||
chr12:131904772 | T | A | 6 | a0001c0010t0002g0207 a0001c0010t0002g0209 a0001c0010t0002g0218 others(3): Show |
6 | HG01071.hp2 HG01106.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-2120T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131904772 | |||||||
chr12:131905024 | C | T | 2 | a0001c0002t0001g0033 a0001c0002t0001g0061 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.247-1868C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905024 | |||||||
chr12:131905043 | G | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(10): Show |
17 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.247-1849G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905043 | |||||||
chr12:131905327 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(3): Show |
10 | HG02615.hp1 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-1565C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905327 | |||||||
chr12:131905365 | C | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0319 a0001c0001t0001g0320 |
6 | HG02615.hp1 HG02818.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-1527C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905365 | |||||||
chr12:131905371 | CTG | C | 74 | a0001c0002t0001g0008 a0001c0002t0001g0032 a0001c0002t0001g0035 others(71): Show |
75 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.247-1520_247-1519d others(4): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905371 | |||||||
chr12:131905383 | C | T | 19 | a0001c0002t0001g0002 a0001c0002t0001g0033 a0001c0002t0001g0041 others(16): Show |
23 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.247-1509C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905383 | |||||||
chr12:131905392 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.247-1500T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905392 | |||||||
chr12:131905597 | G | A | 1 | a0001c0003t0003g0237 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.247-1295G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905597 | |||||||
chr12:131905729 | T | C | 1 | a0001c0003t0006g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.247-1163T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905729 | |||||||
chr12:131905751 | T | A | 8 | a0001c0002t0001g0042 a0001c0002t0001g0062 a0001c0002t0001g0063 others(5): Show |
8 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.247-1141T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131905751 | |||||||
chr12:131906049 | C | T | 54 | a0001c0002t0001g0032 a0001c0002t0001g0037 a0001c0002t0001g0039 others(51): Show |
54 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.247-843C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906049 | |||||||
chr12:131906096 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.247-796C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906096 | |||||||
chr12:131906098 | T | C | 1 | a0001c0001t0002g0144 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.247-794T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906098 | |||||||
chr12:131906102 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.247-790C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906102 | |||||||
chr12:131906120 | G | A | 1 | a0010c0028t0002g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247-772G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906120 | |||||||
chr12:131906188 | G | A | 69 | a0001c0001t0002g0270 a0001c0001t0002g0271 a0001c0001t0002g0272 others(66): Show |
73 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.247-704G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906188 | |||||||
chr12:131906282 | G | A | 3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | HG01891.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.247-610G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906282 | |||||||
chr12:131906508 | C | T | 1 | a0001c0003t0003g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.247-384C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906508 | |||||||
chr12:131906512 | G | T | 1 | a0001c0005t0001g0204 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.247-380G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906512 | |||||||
chr12:131906557 | G | C | 1 | a0001c0003t0003g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.247-335G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906557 | |||||||
chr12:131906561 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(171): Show |
187 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.247-331C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906561 | |||||||
chr12:131906654 | T | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.247-238T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906654 | |||||||
chr12:131906671 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.247-221G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906671 | |||||||
chr12:131906818 | G | A | 1 | a0001c0002t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247-74G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906818 | |||||||
chr12:131906829 | A | C | 2 | a0001c0003t0003g0266 a0001c0003t0006g0267 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.247-63A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906829 | |||||||
chr12:131906866 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0017g0143 |
2 | HG02738.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.247-26C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 3/27 | chr12 | 131906866 | |||||||
chr12:131907049 | C | T | 3 | a0001c0002t0002g0304 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG00733.hp1 HG01175.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.279+125C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907049 | |||||||
chr12:131907055 | C | T | 1 | a0001c0003t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.279+131C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907055 | |||||||
chr12:131907079 | C | T | 1 | a0001c0003t0003g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.279+155C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907079 | |||||||
chr12:131907137 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.279+213T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907137 | |||||||
chr12:131907170 | C | T | 1 | a0003c0027t0001g0109 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.279+246C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907170 | |||||||
chr12:131907181 | G | A | 2 | a0001c0002t0001g0033 a0001c0002t0001g0061 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.279+257G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907181 | |||||||
chr12:131907289 | C | T | 1 | a0001c0003t0006g0267 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.280-206C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907289 | |||||||
chr12:131907331 | T | C | 3 | a0001c0005t0001g0138 a0001c0005t0001g0151 a0001c0005t0001g0204 |
3 | HG01255.hp1 HG02293.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.280-164T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 4/27 | chr12 | 131907331 | |||||||
chr12:131907582 | G | A | 1 | a0001c0005t0001g0152 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.316+51G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907582 | |||||||
chr12:131907602 | C | T | 1 | a0001c0001t0015g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.316+71C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907602 | |||||||
chr12:131907626 | G | C | 6 | a0001c0002t0001g0119 a0001c0009t0005g0018 a0001c0009t0005g0113 others(3): Show |
6 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+95G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907626 | |||||||
chr12:131907776 | T | C | 1 | a0001c0003t0002g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.316+245T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907776 | |||||||
chr12:131907845 | C | G | 1 | a0002c0011t0004g0027 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.316+314C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907845 | |||||||
chr12:131907930 | G | T | 1 | a0001c0002t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.316+399G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131907930 | |||||||
chr12:131907998 | C | CG | 5 | a0001c0001t0002g0147 a0001c0003t0003g0241 a0001c0003t0006g0267 others(2): Show |
5 | HG00408.hp1 HG00558.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+472dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 131907998 | ||||||
chr12:131908067 | TC | T | 6 | a0001c0002t0001g0119 a0001c0009t0005g0018 a0001c0009t0005g0113 others(3): Show |
6 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+538delC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | INFO_REALIGN_3_PRIME | chr12 | 131908067 | ||||||
chr12:131908271 | CTG | C | 6 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0052 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.317-372_317-371del others(2): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 5/27 | chr12 | 131908271 | |||||||
chr12:131908833 | G | A | 1 | a0002c0004t0004g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.490+16G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 6/27 | chr12 | 131908833 | |||||||
chr12:131908839 | C | T | 1 | a0001c0002t0001g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.490+22C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 6/27 | chr12 | 131908839 | |||||||
chr12:131908996 | G | A | 16 | a0001c0002t0001g0032 a0001c0002t0001g0042 a0001c0002t0001g0062 others(13): Show |
16 | HG01106.hp1 HG01175.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.564+25G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 7/27 | chr12 | 131908996 | |||||||
chr12:131909060 | T | C | 3 | a0001c0002t0002g0304 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG00733.hp1 HG01175.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.565-76T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 7/27 | chr12 | 131909060 | |||||||
chr12:131909314 | C | T | 3 | a0001c0001t0002g0142 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | NA18944.hp1 NA18956.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.666+77C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909314 | |||||||
chr12:131909492 | G | A | 1 | a0001c0002t0003g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.666+255G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909492 | |||||||
chr12:131909534 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.667-241C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909534 | |||||||
chr12:131909588 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.667-187C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909588 | |||||||
chr12:131909662 | C | CG | 8 | a0001c0002t0002g0304 a0001c0002t0002g0311 a0001c0002t0002g0316 others(5): Show |
8 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-110dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr12 | 131909662 | ||||||
chr12:131909670 | G | T | 1 | a0001c0003t0003g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.667-105G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909670 | |||||||
chr12:131909682 | G | T | 6 | a0001c0002t0001g0119 a0001c0009t0005g0018 a0001c0009t0005g0113 others(3): Show |
6 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-93G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909682 | |||||||
chr12:131909708 | C | G | 1 | a0001c0010t0002g0209 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.667-67C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909708 | |||||||
chr12:131909769 | C | T | 1 | a0001c0003t0003g0291 | 1 | NA19063.hp2 | splice_region_variant&intron_variant | LOW | c.667-6C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 8/27 | chr12 | 131909769 | |||||||
chr12:131909878 | GC | G | 4 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.726-37delC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr12 | 131909878 | ||||||
chr12:131909881 | C | A | 4 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.726-38C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 9/27 | chr12 | 131909881 | |||||||
chr12:131910077 | C | T | 8 | a0001c0002t0002g0304 a0001c0002t0002g0311 a0001c0002t0002g0316 others(5): Show |
8 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.808+76C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 10/27 | chr12 | 131910077 | |||||||
chr12:131910147 | C | T | 84 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(81): Show |
89 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(86): Show |
intron_variant | MODIFIER | c.809-107C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 10/27 | chr12 | 131910147 | |||||||
chr12:131910217 | G | T | 1 | a0001c0003t0003g0265 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.809-37G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 10/27 | chr12 | 131910217 | |||||||
chr12:131910317 | G | C | 1 | a0002c0004t0004g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.859+13G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 11/27 | chr12 | 131910317 | |||||||
chr12:131910415 | G | A | 5 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(2): Show |
5 | HG01891.hp1 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+111G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 11/27 | chr12 | 131910415 | |||||||
chr12:131910468 | G | A | 1 | a0006c0036t0004g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.859+164G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 11/27 | chr12 | 131910468 | |||||||
chr12:131910507 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(141): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.859+203G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 11/27 | chr12 | 131910507 | |||||||
chr12:131910654 | C | G | 8 | a0001c0002t0002g0304 a0001c0002t0002g0311 a0001c0002t0002g0316 others(5): Show |
8 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.860-58C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 11/27 | chr12 | 131910654 | |||||||
chr12:131910864 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.948+64C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131910864 | |||||||
chr12:131910903 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.948+103G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131910903 | |||||||
chr12:131911073 | G | A | 8 | a0001c0002t0002g0304 a0001c0002t0002g0311 a0001c0002t0002g0316 others(5): Show |
8 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.948+273G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911073 | |||||||
chr12:131911122 | C | T | 5 | a0001c0003t0003g0236 a0001c0003t0003g0239 a0001c0003t0003g0282 others(2): Show |
5 | HG00558.hp2 HG02040.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+322C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911122 | |||||||
chr12:131911234 | C | T | 6 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0052 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.948+434C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911234 | |||||||
chr12:131911255 | G | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.948+455G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911255 | |||||||
chr12:131911428 | T | C | 1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.949-514T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911428 | |||||||
chr12:131911723 | C | G | 1 | a0001c0003t0016g0279 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.949-219C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911723 | |||||||
chr12:131911723 | C | T | 65 | a0001c0003t0002g0244 a0001c0003t0003g0014 a0001c0003t0003g0015 others(62): Show |
69 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.949-219C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911723 | |||||||
chr12:131911729 | G | GC | 4 | a0002c0004t0004g0013 a0002c0004t0004g0212 a0002c0004t0004g0213 others(1): Show |
5 | HG01243.hp1 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.949-211dupC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 131911729 | ||||||
chr12:131911798 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(140): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.949-144C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911798 | |||||||
chr12:131911854 | G | A | 2 | a0001c0006t0004g0268 a0002c0004t0004g0269 |
2 | HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.949-88G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 12/27 | chr12 | 131911854 | |||||||
chr12:131912096 | GGGCACGC others(5): Show |
G | 1 | a0002c0011t0004g0026 | 1 | NA18998.hp1 | splice_region_variant&intron_variant | LOW | c.1096+8_1096+19delG others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912096 | |||||||
chr12:131912105 | G | A | 1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1096+16G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912105 | |||||||
chr12:131912133 | C | CG | 4 | a0001c0001t0002g0187 a0001c0003t0003g0263 a0001c0003t0003g0281 others(1): Show |
4 | HG00438.hp2 HG00735.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1096+48dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr12 | 131912133 | ||||||
chr12:131912134 | G | A | 85 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(82): Show |
90 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.1096+45G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912134 | |||||||
chr12:131912630 | G | A | 1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1096+541G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912630 | |||||||
chr12:131912660 | G | A | 5 | a0001c0003t0002g0244 a0001c0003t0003g0229 a0001c0003t0003g0230 others(2): Show |
5 | HG00558.hp1 HG00597.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1097-538G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912660 | |||||||
chr12:131912669 | G | A | 66 | a0001c0003t0002g0244 a0001c0003t0003g0014 a0001c0003t0003g0015 others(63): Show |
70 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1097-529G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912669 | |||||||
chr12:131912672 | T | G | 3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | HG01891.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1097-526T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912672 | |||||||
chr12:131912676 | C | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(142): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1097-522C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912676 | |||||||
chr12:131912694 | C | G | 1 | a0001c0003t0009g0005 | 3 | NA18947.hp2 NA18982.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1097-504C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912694 | |||||||
chr12:131912913 | A | T | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-285A>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912913 | |||||||
chr12:131912940 | G | C | 1 | a0002c0004t0022g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1097-258G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912940 | |||||||
chr12:131912964 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(310): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1097-234T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912964 | |||||||
chr12:131912965 | G | C | 1 | a0002c0008t0025g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1097-233G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912965 | |||||||
chr12:131912968 | G | T | 1 | a0002c0004t0004g0213 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1097-230G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912968 | |||||||
chr12:131912979 | G | A | 2 | a0001c0003t0003g0227 a0001c0003t0003g0275 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1097-219G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912979 | |||||||
chr12:131912988 | G | A | 71 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 others(68): Show |
75 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.1097-210G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131912988 | |||||||
chr12:131913031 | C | G | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1097-167C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131913031 | |||||||
chr12:131913159 | C | T | 2 | a0001c0003t0003g0227 a0001c0003t0003g0275 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1097-39C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131913159 | |||||||
chr12:131913189 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1097-9C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 13/27 | chr12 | 131913189 | |||||||
chr12:131913347 | G | A | 1 | a0001c0003t0003g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1157+89G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913347 | |||||||
chr12:131913413 | C | T | 97 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(94): Show |
102 | HG00438.hp1 HG00597.hp2 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.1157+155C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913413 | |||||||
chr12:131913421 | C | T | 3 | a0001c0003t0002g0313 a0001c0003t0002g0314 a0003c0014t0001g0310 |
3 | HG02258.hp2 HG02559.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1157+163C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913421 | |||||||
chr12:131913422 | G | A | 4 | a0001c0003t0012g0302 a0001c0013t0012g0303 a0002c0004t0002g0155 others(1): Show |
4 | HG02293.hp1 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1157+164G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913422 | |||||||
chr12:131913491 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1157+233T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913491 | |||||||
chr12:131913564 | G | T | 68 | a0001c0003t0002g0244 a0001c0003t0003g0014 a0001c0003t0003g0015 others(65): Show |
72 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1158-183G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913564 | |||||||
chr12:131913597 | C | G | 73 | a0001c0002t0001g0119 a0001c0003t0002g0244 a0001c0003t0003g0014 others(70): Show |
77 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.1158-150C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913597 | |||||||
chr12:131913610 | C | T | 66 | a0001c0003t0002g0244 a0001c0003t0003g0014 a0001c0003t0003g0015 others(63): Show |
70 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.1158-137C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913610 | |||||||
chr12:131913702 | C | CA | 20 | a0001c0001t0002g0115 a0001c0001t0002g0122 a0001c0001t0002g0142 others(17): Show |
20 | HG01109.hp1 HG02055.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.1158-37dupA | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 131913702 | ||||||
chr12:131913703 | A | C | 16 | a0001c0002t0001g0032 a0001c0002t0001g0042 a0001c0002t0001g0062 others(13): Show |
16 | HG01106.hp1 HG01175.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1158-44A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913703 | |||||||
chr12:131913710 | AC | A | 67 | a0001c0002t0001g0088 a0001c0003t0002g0244 a0001c0003t0003g0014 others(64): Show |
69 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.1158-36delC | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913710 | |||||||
chr12:131913711 | C | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(250): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1158-36C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 14/27 | chr12 | 131913711 | |||||||
chr12:131913884 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1247+48G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/27 | chr12 | 131913884 | |||||||
chr12:131913946 | T | G | 1 | a0001c0002t0001g0071 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1247+110T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/27 | chr12 | 131913946 | |||||||
chr12:131914075 | TCGAG | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(241): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1247+241_1247+244d others(6): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 131914075 | ||||||
chr12:131914179 | G | C | 1 | a0001c0002t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1248-173G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/27 | chr12 | 131914179 | |||||||
chr12:131914293 | T | A | 1 | a0001c0003t0003g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1248-59T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 15/27 | chr12 | 131914293 | |||||||
chr12:131914506 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1373+29C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914506 | |||||||
chr12:131914520 | T | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(56): Show |
64 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1373+43T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914520 | |||||||
chr12:131914599 | C | T | 1 | a0001c0009t0005g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1373+122C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914599 | |||||||
chr12:131914698 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(141): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1373+221A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914698 | |||||||
chr12:131914767 | C | G | 1 | a0002c0008t0004g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1373+290C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914767 | |||||||
chr12:131914776 | C | T | 1 | a0001c0019t0001g0081 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1373+299C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914776 | |||||||
chr12:131914830 | C | T | 91 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0032 others(88): Show |
96 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(93): Show |
intron_variant | MODIFIER | c.1374-253C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914830 | |||||||
chr12:131914841 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(317): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1374-242A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131914841 | |||||||
chr12:131914980 | GGGCCTCC others(62): Show |
G | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1374-85_1374-17del others(69): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr12 | 131914980 | ||||||
chr12:131915023 | C | T | 1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1374-60C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 16/27 | chr12 | 131915023 | |||||||
chr12:131915253 | T | C | 1 | a0001c0006t0003g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1522+22T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 17/27 | chr12 | 131915253 | |||||||
chr12:131915439 | G | T | 1 | a0001c0003t0003g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1609+18G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915439 | |||||||
chr12:131915483 | C | G | 7 | a0001c0002t0001g0047 a0001c0002t0001g0119 a0001c0009t0005g0018 others(4): Show |
7 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609+62C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915483 | |||||||
chr12:131915533 | C | G | 1 | a0001c0002t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1609+112C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915533 | |||||||
chr12:131915621 | C | T | 1 | a0002c0004t0004g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1609+200C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915621 | |||||||
chr12:131915713 | GAGCCGAG others(25): Show |
G | 1 | a0001c0002t0001g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1610-176_1610-145d others(34): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 131915713 | ||||||
chr12:131915756 | G | A | 1 | a0001c0003t0003g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1610-135G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915756 | |||||||
chr12:131915764 | G | A | 133 | a0001c0001t0001g0196 a0001c0002t0001g0032 a0001c0002t0001g0033 others(130): Show |
139 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1610-127G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915764 | |||||||
chr12:131915779 | A | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1610-112A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915779 | |||||||
chr12:131915800 | C | T | 2 | a0002c0004t0004g0185 a0002c0008t0004g0135 |
2 | HG03139.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1610-91C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915800 | |||||||
chr12:131915871 | C | T | 6 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0052 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1610-20C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915871 | |||||||
chr12:131915875 | G | A | 6 | a0001c0002t0001g0119 a0001c0009t0005g0018 a0001c0009t0005g0113 others(3): Show |
6 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1610-16G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 18/27 | chr12 | 131915875 | |||||||
chr12:131916238 | C | T | 4 | a0001c0003t0002g0312 a0001c0003t0002g0313 a0001c0003t0002g0315 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1878+79C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/27 | chr12 | 131916238 | |||||||
chr12:131916269 | C | A | 6 | a0001c0002t0001g0119 a0001c0009t0005g0018 a0001c0009t0005g0113 others(3): Show |
6 | HG00280.hp1 HG02056.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.1878+110C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 19/27 | chr12 | 131916269 | |||||||
chr12:131916617 | C | T | 1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2072+26C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916617 | |||||||
chr12:131916781 | C | T | 1 | a0001c0002t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2073-172C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916781 | |||||||
chr12:131916793 | C | T | 32 | a0001c0002t0001g0035 a0001c0002t0001g0037 a0001c0002t0001g0043 others(29): Show |
32 | HG00597.hp2 HG02055.hp2 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.2073-160C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916793 | |||||||
chr12:131916798 | T | C | 2 | a0001c0005t0002g0156 a0001c0005t0002g0170 |
2 | NA18945.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2073-155T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916798 | |||||||
chr12:131916813 | T | TG | 4 | a0001c0001t0002g0298 a0001c0002t0001g0094 a0001c0003t0016g0279 others(1): Show |
4 | NA18998.hp1 NA19012.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2073-136dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | INFO_REALIGN_3_PRIME | chr12 | 131916813 | ||||||
chr12:131916827 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2073-126C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916827 | |||||||
chr12:131916856 | C | T | 1 | a0001c0006t0028g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2073-97C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916856 | |||||||
chr12:131916919 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2073-34C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 20/27 | chr12 | 131916919 | |||||||
chr12:131917075 | G | GTGGGGCT others(666): Show |
1 | a0001c0001t0002g0200 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(673): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(1869): Show |
1 | a0001c0001t0002g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1876): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(46): Show |
2 | a0001c0006t0004g0268 a0002c0004t0004g0157 |
2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(53): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(297): Show |
1 | a0002c0004t0023g0145 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(304): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(541): Show |
1 | a0002c0011t0004g0027 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(548): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(149): Show |
1 | a0002c0004t0022g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(156): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(181): Show |
1 | a0002c0004t0004g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(188): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(67): Show |
1 | a0002c0008t0004g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(74): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(234): Show |
1 | a0002c0004t0004g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(241): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(370): Show |
1 | a0005c0034t0004g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(377): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917075 | G | GTGGGGCT others(318): Show |
1 | a0002c0004t0004g0013 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(325): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917075 | ||||||
chr12:131917078 | G | GGGCTCGG others(1530): Show |
1 | a0001c0001t0021g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1537): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917078 | ||||||
chr12:131917078 | G | GGGCTCGG others(57): Show |
1 | a0001c0032t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917078 | ||||||
chr12:131917078 | G | GGGCTCGG others(506): Show |
1 | a0002c0004t0004g0213 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(513): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917078 | ||||||
chr12:131917078 | G | GGGCTCGG others(308): Show |
1 | a0002c0004t0004g0212 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(315): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917078 | ||||||
chr12:131917079 | G | GGCTCGGA others(782): Show |
1 | a0001c0001t0002g0299 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(789): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917079 | ||||||
chr12:131917081 | C | CTCGGAGG others(651): Show |
1 | a0001c0006t0003g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(658): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(77): Show |
4 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(1): Show |
4 | HG01928.hp1 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(84): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1162): Show |
1 | a0001c0001t0002g0298 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1169): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(308): Show |
1 | a0001c0001t0002g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(315): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(140): Show |
1 | a0001c0001t0002g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(147): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(182): Show |
1 | a0001c0003t0003g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(189): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(2691): Show |
1 | a0001c0001t0002g0270 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(2698): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(308): Show |
1 | a0001c0001t0007g0159 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(315): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1412): Show |
2 | a0002c0008t0004g0130 a0002c0008t0004g0131 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(1419): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1194): Show |
1 | a0002c0008t0004g0025 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1201): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1142): Show |
1 | a0002c0004t0003g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1149): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(150): Show |
1 | a0001c0006t0028g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(157): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1503): Show |
1 | a0002c0004t0004g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1510): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(46): Show |
1 | a0002c0004t0004g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(53): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(265): Show |
1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(272): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(66): Show |
1 | a0002c0008t0025g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(73): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(129): Show |
1 | a0002c0004t0004g0012 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(136): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(465): Show |
1 | a0002c0004t0002g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(472): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(2948): Show |
1 | a0001c0006t0004g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(2955): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(181): Show |
1 | a0001c0001t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(188): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(319): Show |
1 | a0002c0008t0004g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(326): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTCGGAGG others(1900): Show |
1 | a0001c0003t0003g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2182+41_2182+42ins others(1907): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTTGGAGG others(77): Show |
1 | a0001c0002t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2182+20_2182+21ins others(84): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | CTTGGAGG others(1155): Show |
1 | a0001c0002t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2182+20_2182+21ins others(1162): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | C | G | 1 | a0001c0003t0003g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2182+19C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917081 | |||||||
chr12:131917081 | CTCGGAGG others(35): Show |
C | 13 | a0001c0001t0001g0197 a0001c0001t0001g0318 a0001c0005t0001g0138 others(10): Show |
13 | HG01255.hp1 HG02004.hp2 HG02293.hp2 others(10): Show |
intron_variant | MODIFIER | c.2182+61_2182+102de others(43): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917081 | CTCGGAGG others(56): Show |
C | 1 | a0001c0002t0002g0304 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2182+40_2182+102de others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917081 | ||||||
chr12:131917083 | C | CGGAGGCT others(337): Show |
1 | a0002c0011t0004g0026 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(344): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917083 | ||||||
chr12:131917083 | C | T | 22 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0043 others(19): Show |
22 | HG00438.hp1 HG00597.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.2182+21C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917083 | |||||||
chr12:131917084 | G | GGAGGCTG others(45): Show |
1 | a0002c0004t0004g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(52): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917084 | G | GGAGGCTG others(762): Show |
1 | a0002c0011t0004g0024 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(769): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917084 | G | GGAGGCTG others(1226): Show |
1 | a0002c0004t0003g0180 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(1233): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917084 | G | GGAGGCTG others(234): Show |
1 | a0002c0004t0004g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(241): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917084 | G | GGAGGCTG others(45): Show |
2 | a0002c0004t0004g0177 a0002c0025t0001g0080 |
2 | HG03239.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2182+34_2182+35ins others(52): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917084 | G | GGAGGCTG others(843): Show |
1 | a0002c0004t0004g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2182+34_2182+35ins others(850): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917084 | ||||||
chr12:131917097 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0011 others(80): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(85): Show |
intron_variant | MODIFIER | c.2182+35T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917097 | |||||||
chr12:131917097 | TGGGGGTC others(160): Show |
T | 1 | a0001c0002t0001g0071 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2182+45_2183-138de others(1): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917097 | ||||||
chr12:131917102 | G | C | 40 | a0001c0001t0002g0270 a0001c0002t0001g0032 a0001c0002t0001g0039 others(37): Show |
42 | HG00733.hp1 HG00735.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.2182+40G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917102 | |||||||
chr12:131917102 | G | GTCGGAGG others(25): Show |
1 | a0001c0007t0001g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2182+55_2182+56ins others(32): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGAGG others(215): Show |
1 | a0001c0001t0001g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2182+60_2182+61ins others(222): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGGG others(4): Show |
2 | a0001c0002t0001g0097 a0002c0004t0004g0269 |
2 | HG01099.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2182+44_2182+45ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTG others(4): Show |
1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTG others(3108): Show |
1 | a0001c0002t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(3115): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTG others(856): Show |
1 | a0001c0009t0005g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(863): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTG others(1924): Show |
1 | a0001c0009t0005g0118 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(1931): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(4): Show |
5 | a0001c0002t0001g0044 a0001c0002t0001g0072 a0001c0002t0001g0307 others(2): Show |
5 | HG00597.hp2 HG03654.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182+44_2182+45ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(36): Show |
1 | a0001c0002t0001g0075 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(43): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(132): Show |
1 | a0001c0002t0013g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(139): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(164): Show |
1 | a0001c0003t0001g0046 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(171): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(836): Show |
1 | a0001c0003t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(843): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(164): Show |
1 | a0003c0027t0001g0109 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(171): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(1348): Show |
1 | a0001c0002t0001g0035 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(1355): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(964): Show |
1 | a0001c0002t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(971): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(36): Show |
1 | a0001c0002t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(43): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(197): Show |
1 | a0001c0018t0001g0034 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(204): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(196): Show |
3 | a0001c0002t0001g0043 a0001c0002t0001g0078 a0001c0002t0001g0110 |
3 | NA18956.hp1 NA18960.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2182+44_2182+45ins others(203): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(697): Show |
1 | a0001c0012t0001g0076 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(704): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(452): Show |
1 | a0001c0012t0001g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(459): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTCGGGTT others(697): Show |
1 | a0001c0003t0003g0290 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(704): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTTGGGGG others(4): Show |
1 | a0002c0033t0002g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2182+41_2182+42ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTTGGGGG others(801): Show |
1 | a0001c0006t0004g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2182+41_2182+42ins others(808): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTTGGGGG others(865): Show |
1 | a0001c0006t0004g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2182+41_2182+42ins others(872): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917102 | G | GTTGGGGG others(654): Show |
1 | a0002c0004t0004g0214 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2182+41_2182+42ins others(661): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917102 | ||||||
chr12:131917104 | C | CGGGTGGG others(4): Show |
2 | a0001c0002t0001g0008 a0001c0002t0001g0305 |
2 | HG03471.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2182+44_2182+45ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | CGGGTGGG others(356): Show |
1 | a0001c0002t0001g0008 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(363): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | CGGGTTCG others(932): Show |
1 | a0001c0002t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(939): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | CGGGTTCG others(292): Show |
1 | a0001c0002t0001g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(299): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | CGGGTTCG others(772): Show |
1 | a0001c0002t0001g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(779): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | CGGGTTCG others(292): Show |
1 | a0001c0002t0001g0104 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(299): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | C | T | 1 | a0002c0011t0004g0024 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2182+42C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917104 | |||||||
chr12:131917104 | CG | C | 22 | a0001c0002t0001g0032 a0001c0002t0001g0039 a0001c0002t0001g0062 others(19): Show |
22 | HG00733.hp1 HG01106.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2182+44delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917104 | CGGAGGCT others(3): Show |
C | 1 | a0001c0002t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2182+46_2182+55del others(10): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917104 | ||||||
chr12:131917105 | G | GGAGGCTG others(359): Show |
1 | a0002c0008t0004g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2182+55_2182+56ins others(366): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917105 | ||||||
chr12:131917105 | G | GGAGGCTG others(121): Show |
1 | a0003c0014t0001g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2182+55_2182+56ins others(128): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917105 | ||||||
chr12:131917105 | G | GGGGGGAG others(86): Show |
1 | a0002c0004t0004g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(93): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917105 | ||||||
chr12:131917105 | G | GGGGGGAG others(160): Show |
1 | a0002c0004t0004g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(167): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917105 | ||||||
chr12:131917105 | G | GGGTGGGG others(3): Show |
1 | a0001c0002t0002g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2182+44_2182+45ins others(10): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917105 | ||||||
chr12:131917117 | A | ACGGGGGT others(4): Show |
15 | a0001c0002t0001g0044 a0001c0002t0001g0062 a0001c0002t0001g0063 others(12): Show |
16 | HG00597.hp2 HG01175.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2182+55_2182+56ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917117 | |||||||
chr12:131917117 | A | ACGGGGGT others(100): Show |
1 | a0001c0002t0001g0066 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2182+55_2182+56ins others(107): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917117 | |||||||
chr12:131917117 | A | ACGGGGGT others(356): Show |
1 | a0001c0002t0001g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2182+55_2182+56ins others(363): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917117 | |||||||
chr12:131917117 | A | ATGGGGCT others(24): Show |
2 | a0001c0001t0001g0182 a0001c0005t0001g0203 |
2 | HG02258.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2182+60_2182+61ins others(31): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917117 | ||||||
chr12:131917117 | A | G | 1 | a0001c0002t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2182+55A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917117 | |||||||
chr12:131917118 | T | C | 47 | a0001c0001t0002g0004 a0001c0001t0002g0126 a0001c0001t0002g0144 others(44): Show |
51 | HG00733.hp1 HG00735.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.2182+56T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917118 | |||||||
chr12:131917118 | T | TGGGGCTC others(476): Show |
1 | a0001c0001t0002g0161 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2182+60_2182+61ins others(483): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917118 | ||||||
chr12:131917118 | T | TGGGGCTC others(468): Show |
1 | a0001c0006t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2182+60_2182+61ins others(475): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917118 | ||||||
chr12:131917120 | G | GGGCTCGA others(109): Show |
1 | a0001c0001t0001g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2182+60_2182+61ins others(116): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917120 | ||||||
chr12:131917120 | G | GGGCTCGG others(141): Show |
1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2182+60_2182+61ins others(148): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917120 | ||||||
chr12:131917123 | G | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(92): Show |
108 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.2182+61G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917123 | |||||||
chr12:131917123 | G | GTCGGAGG others(14): Show |
1 | a0001c0002t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2182+81_2182+82ins others(21): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGGG others(4): Show |
3 | a0001c0003t0002g0313 a0001c0003t0002g0314 a0002c0004t0004g0021 |
3 | HG02258.hp2 HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2182+65_2182+66ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(4): Show |
1 | a0003c0027t0001g0109 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(4): Show |
1 | a0001c0002t0001g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(1060): Show |
1 | a0001c0002t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(1067): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(292): Show |
1 | a0001c0002t0002g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(299): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(132): Show |
1 | a0001c0002t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(139): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(132): Show |
1 | a0001c0002t0002g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(139): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(569): Show |
1 | a0001c0002t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(576): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(36): Show |
1 | a0001c0002t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(43): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(57): Show |
1 | a0001c0007t0011g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTG others(1214): Show |
1 | a0001c0002t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(1221): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTT others(4): Show |
16 | a0001c0002t0001g0035 a0001c0002t0001g0043 a0001c0002t0001g0072 others(13): Show |
16 | HG00280.hp1 HG01891.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.2182+65_2182+66ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917123 | G | GTCGGGTT others(68): Show |
2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+65_2182+66ins others(75): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917123 | ||||||
chr12:131917125 | C | CGGAGGCT others(877): Show |
1 | a0010c0028t0002g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2182+81_2182+82ins others(884): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | CGGAGGCT others(25): Show |
1 | a0001c0002t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(32): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | CGGGTGGG others(4): Show |
7 | a0001c0002t0001g0008 a0001c0002t0001g0039 a0001c0002t0001g0050 others(4): Show |
8 | HG01175.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2182+65_2182+66ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | CGGGTGGG others(67): Show |
1 | a0001c0002t0002g0316 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(74): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | CGGGTGGG others(1059): Show |
1 | a0001c0002t0003g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(1066): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | CGGGTTCG others(548): Show |
1 | a0001c0002t0002g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(555): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | C | T | 4 | a0001c0001t0002g0137 a0001c0001t0002g0140 a0001c0001t0002g0168 others(1): Show |
4 | HG00280.hp2 NA18747.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182+63C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917125 | |||||||
chr12:131917125 | CG | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0148 others(16): Show |
25 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.2182+65delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | CGGAGGCT others(3): Show |
C | 2 | a0001c0002t0001g0032 a0001c0007t0001g0007 |
3 | HG01106.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2182+67_2182+76del others(10): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | CGGAGGCT others(24): Show |
C | 1 | a0001c0022t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2182+67_2182+97del others(31): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | CGGAGGCT others(66): Show |
C | 1 | a0001c0003t0009g0005 | 3 | NA18947.hp2 NA18982.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2182+82_2182+154de others(74): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | CGGAGGCT others(151): Show |
C | 1 | a0001c0005t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2182+65_2183-127de others(1): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917125 | CGGAGGCT others(183): Show |
C | 1 | a0002c0004t0002g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2182+65_2183-95del | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917125 | ||||||
chr12:131917126 | G | GGGTGGGG others(3): Show |
1 | a0001c0032t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2182+65_2182+66ins others(10): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917126 | ||||||
chr12:131917126 | GGAGGCTG others(34): Show |
G | 1 | a0001c0002t0002g0311 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2182+87_2182+127de others(42): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917126 | ||||||
chr12:131917126 | GGAGGCTG others(86): Show |
G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG01934.hp2 HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2182+77_2182+169de others(94): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917126 | ||||||
chr12:131917132 | T | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+70T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917132 | |||||||
chr12:131917138 | A | ACGGGGGT others(4): Show |
12 | a0001c0001t0001g0196 a0001c0002t0001g0002 a0001c0002t0001g0057 others(9): Show |
14 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2182+76_2182+77ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917138 | |||||||
chr12:131917138 | A | G | 2 | a0001c0002t0001g0032 a0001c0007t0001g0007 |
3 | HG01106.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2182+76A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917138 | |||||||
chr12:131917139 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(75): Show |
86 | HG00597.hp2 HG00609.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.2182+77T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917139 | |||||||
chr12:131917142 | G | A | 1 | a0001c0007t0001g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2182+80G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917142 | |||||||
chr12:131917144 | G | C | 32 | a0001c0001t0001g0196 a0001c0001t0002g0122 a0001c0001t0002g0270 others(29): Show |
35 | HG01071.hp1 HG01106.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.2182+82G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917144 | |||||||
chr12:131917144 | G | GTCGGGAG others(4): Show |
1 | a0001c0007t0001g0055 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGGG others(4): Show |
2 | a0001c0002t0002g0316 a0001c0003t0002g0054 |
2 | HG00733.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTG others(4): Show |
3 | a0001c0002t0001g0085 a0001c0002t0001g0094 a0001c0003t0001g0046 |
3 | HG02486.hp2 NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTG others(196): Show |
1 | a0001c0002t0001g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(203): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTG others(951): Show |
1 | a0001c0002t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(958): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(4): Show |
25 | a0001c0001t0002g0193 a0001c0002t0001g0035 a0001c0002t0001g0043 others(22): Show |
25 | HG00280.hp1 HG00408.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(324): Show |
1 | a0001c0002t0001g0097 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(331): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(36): Show |
1 | a0001c0003t0003g0290 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(43): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(568): Show |
1 | a0001c0002t0001g0068 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(575): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(632): Show |
1 | a0001c0002t0001g0069 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(639): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917144 | G | GTCGGGTT others(4): Show |
1 | a0001c0009t0005g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917144 | ||||||
chr12:131917146 | C | CGGGTGGG others(57): Show |
1 | a0001c0002t0001g0096 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | C | CGGGTGGG others(260): Show |
1 | a0001c0002t0001g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(267): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | C | CGGGTGGG others(4): Show |
8 | a0001c0001t0017g0143 a0001c0002t0001g0008 a0001c0002t0001g0072 others(5): Show |
8 | HG00597.hp2 HG01891.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | C | CGGGTTCG others(196): Show |
1 | a0001c0002t0001g0045 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2182+86_2182+87ins others(203): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | C | CGGGTTCG others(4): Show |
5 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(2): Show |
5 | HG01175.hp1 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182+86_2182+87ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | C | T | 2 | a0001c0002t0001g0053 a0002c0004t0004g0012 |
3 | HG01074.hp1 HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2182+84C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917146 | |||||||
chr12:131917146 | CG | C | 3 | a0001c0002t0002g0093 a0001c0003t0002g0313 a0001c0003t0002g0314 |
3 | HG02258.hp2 HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2182+86delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | CGGAGGCT others(3): Show |
C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0148 others(10): Show |
17 | HG01099.hp1 HG01175.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.2182+88_2182+97del others(10): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917146 | CGGAGGCT others(55): Show |
C | 1 | a0001c0001t0001g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2182+88_2182+149de others(63): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917146 | ||||||
chr12:131917153 | T | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+91T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917153 | |||||||
chr12:131917155 | T | TGGGACGG others(69): Show |
1 | a0001c0002t0001g0008 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2182+97_2182+98ins others(76): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917155 | ||||||
chr12:131917159 | A | ACGGGGGT others(1265): Show |
1 | a0001c0001t0002g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2182+97_2182+98ins others(1272): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917159 | A | ACGGGGGT others(4): Show |
6 | a0001c0002t0001g0084 a0001c0002t0001g0097 a0001c0002t0001g0119 others(3): Show |
6 | HG00280.hp1 HG01099.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182+97_2182+98ins others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917159 | A | ACGGGGGT others(109): Show |
1 | a0001c0007t0001g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2182+97_2182+98ins others(116): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917159 | A | ACGGGGGT others(580): Show |
1 | a0001c0002t0002g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2182+97_2182+98ins others(587): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917159 | A | ACGGGGGT others(228): Show |
1 | a0001c0002t0003g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2182+97_2182+98ins others(235): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917159 | A | ATGGGGGT others(1556): Show |
1 | a0001c0003t0003g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2182+102_2182+103i others(1565): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917159 | ||||||
chr12:131917159 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0148 others(11): Show |
18 | HG01099.hp1 HG01175.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2182+97A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917159 | |||||||
chr12:131917160 | T | C | 30 | a0001c0001t0002g0160 a0001c0001t0002g0178 a0001c0001t0002g0187 others(27): Show |
31 | HG00099.hp1 HG00733.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2182+98T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917160 | |||||||
chr12:131917164 | G | C | 1 | a0001c0002t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2182+102G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917164 | |||||||
chr12:131917165 | C | G | 179 | a0001c0001t0001g0196 a0001c0001t0001g0201 a0001c0001t0002g0004 others(176): Show |
186 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.2182+103C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917165 | |||||||
chr12:131917165 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2182+103C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917165 | |||||||
chr12:131917167 | C | CG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0134 others(111): Show |
125 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2182+106dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGAGGCTG others(57): Show |
1 | a0002c0008t0004g0135 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2182+117_2182+118i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGAGGCTG others(46): Show |
1 | a0002c0008t0025g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2182+122_2182+123i others(55): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGAGGCTG others(737): Show |
1 | a0001c0003t0002g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2182+126_2182+127i others(746): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(131): Show |
1 | a0001c0010t0002g0209 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(140): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(206): Show |
1 | a0001c0001t0002g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(215): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(869): Show |
1 | a0001c0001t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(878): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(278): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0139 |
4 | HG00609.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182+106_2182+107i others(287): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(2936): Show |
1 | a0001c0009t0005g0113 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2945): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1596): Show |
1 | a0001c0001t0002g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1605): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1038): Show |
1 | a0001c0001t0002g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1047): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(2616): Show |
1 | a0001c0001t0002g0189 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2625): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(377): Show |
1 | a0001c0001t0002g0190 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(386): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(2679): Show |
1 | a0001c0001t0002g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2688): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(3331): Show |
1 | a0001c0001t0002g0115 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(3340): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(835): Show |
1 | a0001c0001t0002g0114 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(844): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1047): Show |
1 | a0001c0001t0002g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1056): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(110): Show |
2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | NA18944.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(119): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1564): Show |
1 | a0001c0001t0002g0274 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1573): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(174): Show |
1 | a0001c0010t0002g0218 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(183): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(858): Show |
1 | a0001c0002t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(867): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(15): Show |
3 | a0001c0003t0003g0285 a0001c0003t0006g0222 a0001c0003t0024g0283 |
3 | HG02165.hp1 NA18943.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(24): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(351): Show |
1 | a0001c0001t0002g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(360): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(173): Show |
1 | a0001c0006t0004g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(182): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1439): Show |
1 | a0005c0034t0004g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1448): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1882): Show |
1 | a0001c0003t0003g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1891): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(695): Show |
1 | a0001c0001t0002g0187 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(704): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(111): Show |
1 | a0001c0003t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(120): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(110): Show |
1 | a0002c0008t0004g0183 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(119): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(143): Show |
1 | a0001c0003t0003g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(152): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(3343): Show |
1 | a0001c0002t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(3352): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(152): Show |
1 | a0001c0001t0002g0300 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(161): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(57): Show |
1 | a0001c0003t0003g0278 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(343): Show |
1 | a0001c0003t0003g0265 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(352): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(175): Show |
1 | a0001c0002t0001g0243 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(184): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1570): Show |
1 | a0001c0003t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1579): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(36): Show |
1 | a0001c0003t0003g0291 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(45): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(78): Show |
3 | a0001c0003t0003g0286 a0001c0003t0003g0287 a0001c0003t0016g0279 |
3 | NA19005.hp1 NA19062.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(87): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(216): Show |
1 | a0002c0025t0001g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(225): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(868): Show |
1 | a0001c0002t0011g0038 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(877): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(228): Show |
1 | a0001c0002t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(237): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(822): Show |
1 | a0008c0026t0001g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(831): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(377): Show |
1 | a0001c0002t0001g0100 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(386): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(377): Show |
1 | a0001c0002t0001g0235 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(386): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(164): Show |
1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(173): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(57): Show |
3 | a0001c0003t0002g0244 a0001c0003t0003g0229 a0001c0003t0003g0230 |
3 | HG00597.hp1 NA18959.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1290): Show |
1 | a0001c0003t0003g0249 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1299): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(57): Show |
1 | a0001c0003t0003g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1398): Show |
1 | a0001c0003t0003g0250 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1407): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(440): Show |
1 | a0001c0003t0003g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(449): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(78): Show |
2 | a0001c0003t0003g0255 a0001c0003t0003g0282 |
2 | HG02040.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(87): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(99): Show |
1 | a0001c0003t0014g0264 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(108): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(758): Show |
1 | a0001c0003t0003g0288 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(767): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(343): Show |
1 | a0001c0020t0003g0251 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(352): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(960): Show |
1 | a0001c0003t0003g0252 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(969): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(610): Show |
2 | a0001c0003t0010g0231 a0001c0003t0010g0253 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(619): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(461): Show |
1 | a0001c0003t0003g0237 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(470): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(803): Show |
1 | a0001c0003t0008g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(812): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1218): Show |
1 | a0001c0003t0008g0254 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1227): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(2830): Show |
1 | a0001c0003t0008g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2839): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(1421): Show |
1 | a0001c0003t0006g0267 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1430): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(270): Show |
1 | a0001c0003t0003g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(279): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(472): Show |
2 | a0001c0003t0003g0227 a0001c0003t0003g0275 |
2 | NA18973.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(481): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(526): Show |
1 | a0001c0003t0003g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(535): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(270): Show |
1 | a0001c0003t0003g0257 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(279): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(238): Show |
1 | a0001c0003t0003g0263 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(247): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(643): Show |
1 | a0001c0003t0003g0281 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(652): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(569): Show |
1 | a0001c0003t0003g0258 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(578): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(121): Show |
1 | a0001c0003t0014g0233 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(130): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(409): Show |
2 | a0001c0003t0003g0223 a0001c0003t0003g0240 |
2 | NA18947.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(418): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(377): Show |
1 | a0001c0003t0003g0228 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(386): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGAGGCT others(89): Show |
2 | a0001c0010t0004g0208 a0001c0030t0002g0199 |
2 | HG01981.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(98): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGAGGA others(152): Show |
1 | a0001c0007t0001g0006 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(161): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(5): Show |
2 | a0001c0002t0001g0086 a0001c0003t0003g0293 |
2 | HG02040.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(1253): Show |
1 | a0001c0002t0002g0092 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1262): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(2149): Show |
1 | a0001c0003t0002g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2158): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(1253): Show |
1 | a0001c0002t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1262): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(1124): Show |
1 | a0001c0003t0003g0294 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1133): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(121): Show |
1 | a0001c0003t0003g0236 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(130): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(613): Show |
1 | a0001c0002t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(622): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(3112): Show |
1 | a0001c0009t0005g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(3121): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(377): Show |
1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(386): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(228): Show |
1 | a0001c0019t0001g0081 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(237): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(1679): Show |
1 | a0001c0002t0001g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1688): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(1755): Show |
1 | a0001c0002t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1764): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(5): Show |
3 | a0001c0002t0001g0036 a0001c0002t0013g0074 a0001c0003t0001g0046 |
3 | HG02083.hp2 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(133): Show |
1 | a0001c0002t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(142): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(69): Show |
1 | a0001c0002t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTGGG others(2277): Show |
1 | a0001c0002t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(2286): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(5): Show |
23 | a0001c0001t0017g0143 a0001c0002t0001g0043 a0001c0002t0001g0044 others(20): Show |
23 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2182+106_2182+107i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(485): Show |
1 | a0001c0002t0002g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(494): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(869): Show |
1 | a0001c0002t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(878): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(729): Show |
1 | a0001c0003t0002g0313 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(738): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(1509): Show |
1 | a0001c0002t0001g0072 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1518): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(645): Show |
1 | a0001c0002t0019g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(654): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(805): Show |
1 | a0004c0016t0013g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(814): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(997): Show |
1 | a0001c0002t0001g0035 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(1006): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(101): Show |
1 | a0001c0002t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(110): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(133): Show |
1 | a0001c0012t0001g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(142): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(90): Show |
1 | a0009c0024t0003g0289 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(99): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(5): Show |
2 | a0001c0002t0001g0032 a0001c0002t0001g0047 |
2 | HG01106.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2182+106_2182+107i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(37): Show |
1 | a0001c0002t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2182+106_2182+107i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(261): Show |
1 | a0001c0002t0001g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(270): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | CGGGTTCG others(293): Show |
1 | a0001c0002t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2182+106_2182+107i others(302): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917167 | C | G | 2 | a0001c0002t0001g0039 a0001c0022t0001g0087 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2182+105C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917167 | |||||||
chr12:131917167 | CGAGGCTG others(24): Show |
C | 2 | a0001c0002t0001g0033 a0001c0002t0001g0061 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2182+107_2182+137d others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917167 | ||||||
chr12:131917173 | T | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+111T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917173 | |||||||
chr12:131917179 | ATGGGGGT others(4): Show |
A | 5 | a0001c0002t0001g0057 a0001c0002t0001g0058 a0001c0002t0001g0060 others(2): Show |
5 | HG02293.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182+123_2182+133d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917179 | ||||||
chr12:131917180 | T | C | 85 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0318 others(82): Show |
93 | HG00558.hp1 HG00609.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.2182+118T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917180 | |||||||
chr12:131917184 | G | GCTCGGAG others(3): Show |
8 | a0001c0002t0001g0002 a0001c0002t0001g0041 a0001c0002t0001g0059 others(5): Show |
10 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.2182+122_2182+123i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917184 | |||||||
chr12:131917184 | G | GGGTCGGA others(4): Show |
2 | a0001c0001t0002g0194 a0002c0004t0004g0136 |
2 | HG02572.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2182+123_2182+124i others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917184 | ||||||
chr12:131917184 | G | GGTTGGAG others(3): Show |
2 | a0002c0011t0004g0026 a0002c0011t0004g0027 |
2 | NA18980.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2182+124_2182+125i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917184 | ||||||
chr12:131917185 | G | C | 1 | a0002c0004t0004g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2182+123G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917185 | |||||||
chr12:131917187 | C | CGGAGGCT others(3): Show |
14 | a0001c0001t0001g0148 a0001c0001t0002g0011 a0001c0001t0002g0137 others(11): Show |
15 | HG00408.hp2 HG00609.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2182+127_2182+128i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(806): Show |
1 | a0001c0006t0004g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(815): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(234): Show |
1 | a0001c0023t0003g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(243): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(649): Show |
1 | a0001c0003t0003g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(658): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(276): Show |
1 | a0001c0001t0002g0140 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(285): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(797): Show |
1 | a0001c0003t0003g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(806): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(623): Show |
1 | a0001c0001t0015g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(632): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(66): Show |
1 | a0001c0001t0003g0162 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(75): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(498): Show |
1 | a0001c0001t0002g0163 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(507): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(24): Show |
1 | a0002c0004t0004g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(507): Show |
1 | a0001c0001t0026g0297 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(516): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(1656): Show |
1 | a0002c0004t0004g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(1665): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(45): Show |
1 | a0001c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(54): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(87): Show |
1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(96): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(66): Show |
1 | a0001c0003t0003g0260 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(75): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(192): Show |
1 | a0001c0001t0002g0168 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(201): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(182): Show |
1 | a0002c0004t0004g0030 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(191): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(150): Show |
1 | a0001c0001t0002g0004 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(159): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(171): Show |
2 | a0001c0001t0002g0150 a0001c0035t0007g0004 |
2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2182+127_2182+128i others(180): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(192): Show |
2 | a0001c0001t0002g0004 a0001c0001t0002g0126 |
2 | HG00735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2182+127_2182+128i others(201): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(855): Show |
1 | a0001c0003t0003g0261 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(864): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(413): Show |
1 | a0002c0004t0004g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2182+127_2182+128i others(422): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | CGGAGGCT others(598): Show |
1 | a0002c0004t0004g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2182+127_2182+128i others(607): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917187 | C | G | 12 | a0001c0001t0002g0194 a0001c0002t0001g0002 a0001c0002t0001g0041 others(9): Show |
14 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2182+125C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917187 | |||||||
chr12:131917187 | CGGGTGGG others(4): Show |
C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0176 others(9): Show |
16 | HG01243.hp2 HG01515.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.2182+128_2182+138d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917187 | ||||||
chr12:131917189 | G | GAGGCT | 4 | a0001c0001t0002g0161 a0001c0003t0003g0259 a0002c0004t0004g0141 others(1): Show |
4 | HG02027.hp2 HG02922.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182+127_2182+128i others(7): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917189 | |||||||
chr12:131917190 | G | A | 48 | a0001c0001t0001g0148 a0001c0001t0002g0004 a0001c0001t0002g0011 others(45): Show |
53 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2182+128G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917190 | |||||||
chr12:131917190 | G | GGGGAGCT others(215): Show |
1 | a0001c0001t0002g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2182+128_2182+129i others(224): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917190 | |||||||
chr12:131917190 | G | GTTCGGCT others(35): Show |
1 | a0001c0006t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2182+129_2182+130i others(44): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917190 | ||||||
chr12:131917190 | G | GTTCGGCT others(307): Show |
1 | a0002c0004t0004g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2182+129_2182+130i others(316): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917190 | ||||||
chr12:131917190 | G | GTTCGGCT others(322): Show |
1 | a0001c0002t0002g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2182+129_2182+130i others(331): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917190 | ||||||
chr12:131917191 | T | G | 5 | a0001c0001t0002g0144 a0001c0001t0002g0147 a0001c0003t0018g0247 others(2): Show |
5 | HG01099.hp1 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2182+129T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917191 | |||||||
chr12:131917191 | T | TGGGAC | 4 | a0001c0001t0002g0161 a0001c0003t0003g0259 a0002c0004t0004g0141 others(1): Show |
4 | HG02027.hp2 HG02922.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182+132_2182+133i others(7): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917191 | ||||||
chr12:131917191 | T | TTCGGCTC others(119): Show |
1 | a0001c0001t0002g0200 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2182+129_2182+130i others(128): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917191 | |||||||
chr12:131917192 | G | T | 36 | a0001c0001t0002g0187 a0001c0001t0002g0296 a0001c0001t0002g0298 others(33): Show |
38 | HG00140.hp2 HG00558.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.2182+130G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917192 | |||||||
chr12:131917193 | G | C | 36 | a0001c0001t0002g0187 a0001c0001t0002g0296 a0001c0001t0002g0298 others(33): Show |
38 | HG00140.hp2 HG00558.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.2182+131G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917193 | |||||||
chr12:131917193 | G | GGGCTCGA others(1035): Show |
1 | a0002c0031t0002g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2182+135_2182+136i others(1044): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917193 | ||||||
chr12:131917194 | G | A | 5 | a0001c0001t0002g0144 a0001c0001t0002g0147 a0001c0003t0018g0247 others(2): Show |
5 | HG01099.hp1 HG01192.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2182+132G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917194 | |||||||
chr12:131917196 | C | CTCGGAGG others(326): Show |
1 | a0001c0006t0004g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2182+135_2182+136i others(335): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917196 | ||||||
chr12:131917196 | C | CTCGGAGG others(238): Show |
1 | a0001c0002t0004g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2182+135_2182+136i others(247): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917196 | ||||||
chr12:131917196 | C | CTCGGAGG others(171): Show |
2 | a0002c0008t0004g0130 a0002c0008t0004g0131 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2182+135_2182+136i others(180): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917196 | ||||||
chr12:131917196 | C | CTCGGAGG others(110): Show |
1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2182+135_2182+136i others(119): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917196 | ||||||
chr12:131917196 | C | G | 40 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0126 others(37): Show |
43 | HG00280.hp2 HG00408.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.2182+134C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917196 | |||||||
chr12:131917198 | T | C | 200 | a0001c0001t0001g0134 a0001c0001t0001g0148 a0001c0001t0001g0182 others(197): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2182+136T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917198 | |||||||
chr12:131917198 | T | TGGAGGCT others(236): Show |
1 | a0001c0001t0002g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2182+149_2182+150i others(245): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917198 | ||||||
chr12:131917198 | T | TGGAGGCT others(110): Show |
1 | a0001c0001t0002g0273 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2182+149_2182+150i others(119): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917198 | ||||||
chr12:131917199 | G | C | 2 | a0001c0010t0002g0207 a0002c0004t0002g0172 |
2 | HG00140.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2182+137G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917199 | |||||||
chr12:131917199 | GGAGGCTG others(13): Show |
G | 2 | a0001c0002t0001g0066 a0001c0003t0006g0238 |
2 | HG02523.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2182+150_2182+169d others(22): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917199 | ||||||
chr12:131917201 | A | G | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2182+139A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917201 | |||||||
chr12:131917205 | T | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+143T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917205 | |||||||
chr12:131917207 | T | TGGGATGG others(5): Show |
7 | a0001c0001t0002g0206 a0001c0001t0002g0300 a0001c0006t0004g0149 others(4): Show |
7 | HG01071.hp2 HG01106.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182+154_2182+155i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917207 | ||||||
chr12:131917207 | T | TGGGATGG others(69): Show |
2 | a0001c0001t0001g0201 a0001c0001t0002g0167 |
2 | HG00099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2182+154_2182+155i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917207 | ||||||
chr12:131917211 | A | ACGGGGGT others(4): Show |
8 | a0001c0001t0002g0194 a0001c0001t0007g0159 a0001c0002t0001g0036 others(5): Show |
8 | HG00140.hp1 HG00733.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2182+149_2182+150i others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917211 | |||||||
chr12:131917211 | A | ACGGGGGT others(836): Show |
1 | a0001c0003t0003g0255 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2182+149_2182+150i others(845): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917211 | |||||||
chr12:131917211 | A | ACGGGGGT others(2436): Show |
1 | a0001c0009t0005g0120 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2182+149_2182+150i others(2445): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917211 | |||||||
chr12:131917211 | A | ACGGGGGT others(228): Show |
1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2182+149_2182+150i others(237): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917211 | |||||||
chr12:131917211 | A | ATGGGGCT others(24): Show |
3 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0056 |
5 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2182+169_2182+170i others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917211 | ||||||
chr12:131917211 | A | ATGGGGCT others(24): Show |
1 | a0001c0007t0011g0051 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2182+169_2182+170i others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917211 | ||||||
chr12:131917211 | A | G | 1 | a0001c0001t0001g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2182+149A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917211 | |||||||
chr12:131917212 | T | C | 41 | a0001c0001t0001g0148 a0001c0001t0002g0161 a0001c0001t0002g0299 others(38): Show |
41 | HG00280.hp1 HG00558.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.2182+150T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917212 | |||||||
chr12:131917212 | TGGGGCTC others(13): Show |
T | 1 | a0001c0002t0001g0067 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2182+155_2182+174d others(22): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917212 | ||||||
chr12:131917213 | G | T | 1 | a0001c0001t0001g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2182+151G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917213 | |||||||
chr12:131917214 | G | C | 1 | a0001c0001t0001g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2182+152G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917214 | |||||||
chr12:131917214 | G | GGGGTTGG others(89): Show |
1 | a0001c0006t0003g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2182+154_2182+155i others(98): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917214 | ||||||
chr12:131917217 | C | G | 185 | a0001c0001t0001g0134 a0001c0001t0001g0148 a0001c0001t0001g0318 others(182): Show |
191 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.2182+155C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917217 | |||||||
chr12:131917219 | C | CG | 87 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(84): Show |
96 | HG01099.hp1 HG01109.hp1 HG01109.hp2 others(93): Show |
intron_variant | MODIFIER | c.2182+158dupG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(142): Show |
1 | a0001c0002t0003g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2183-168_2183-167i others(151): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(46): Show |
1 | a0001c0002t0001g0094 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2182+169_2182+170i others(55): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(139): Show |
1 | a0002c0008t0004g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2182+169_2182+170i others(148): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(3673): Show |
1 | a0002c0004t0004g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2182+169_2182+170i others(3682): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(1397): Show |
1 | a0002c0004t0004g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2182+169_2182+170i others(1406): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGAGGCTG others(56): Show |
1 | a0001c0007t0001g0052 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2182+169_2182+170i others(65): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(953): Show |
1 | a0001c0003t0003g0249 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(962): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(154): Show |
1 | a0001c0002t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(163): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(381): Show |
1 | a0002c0011t0004g0027 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(390): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(300): Show |
1 | a0002c0011t0004g0026 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(309): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(88): Show |
1 | a0001c0006t0004g0188 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(97): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(977): Show |
1 | a0002c0004t0003g0171 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(986): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(568): Show |
1 | a0001c0003t0002g0315 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(577): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(120): Show |
1 | a0001c0006t0004g0210 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(129): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(152): Show |
3 | a0002c0004t0004g0212 a0002c0004t0004g0213 a0002c0004t0004g0214 |
3 | HG01243.hp1 HG01433.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(161): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(1756): Show |
2 | a0001c0003t0010g0231 a0001c0003t0010g0253 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(1765): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(686): Show |
1 | a0001c0003t0003g0281 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(695): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(697): Show |
1 | a0001c0003t0003g0292 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(706): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(558): Show |
1 | a0001c0003t0003g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(567): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(356): Show |
1 | a0001c0003t0003g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(365): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(654): Show |
1 | a0002c0004t0003g0180 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(663): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGAGGCT others(446): Show |
1 | a0010c0028t0002g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(455): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGATGG others(246): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0139 |
4 | HG00609.hp2 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2182+158_2182+159i others(255): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGATGG others(90): Show |
1 | a0001c0001t0002g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(99): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGGGCT others(15): Show |
1 | a0002c0004t0004g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(24): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGGGGA others(5): Show |
2 | a0001c0002t0002g0304 a0001c0002t0002g0317 |
2 | HG01175.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGGGGA others(605): Show |
1 | a0001c0001t0002g0299 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(614): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTAGG others(5): Show |
1 | a0001c0002t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(5): Show |
8 | a0001c0001t0002g0190 a0001c0002t0001g0050 a0001c0002t0001g0063 others(5): Show |
8 | HG01261.hp1 HG01981.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(101): Show |
1 | a0001c0002t0001g0235 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(110): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(133): Show |
1 | a0001c0002t0001g0008 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(142): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(709): Show |
1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(718): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(37): Show |
1 | a0001c0012t0001g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(197): Show |
1 | a0001c0002t0001g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(206): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(549): Show |
1 | a0001c0002t0001g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(558): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(1305): Show |
1 | a0001c0003t0003g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1314): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(613): Show |
1 | a0001c0003t0018g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(622): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(250): Show |
1 | a0001c0003t0003g0284 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(259): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(90): Show |
1 | a0001c0002t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(99): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(5): Show |
8 | a0001c0002t0001g0035 a0001c0002t0001g0044 a0001c0002t0001g0045 others(5): Show |
8 | HG00597.hp2 HG02083.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(421): Show |
1 | a0001c0002t0001g0008 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(430): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(325): Show |
1 | a0001c0002t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(334): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(69): Show |
1 | a0001c0002t0001g0072 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(165): Show |
1 | a0001c0002t0001g0104 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(174): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(101): Show |
1 | a0001c0002t0001g0079 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(110): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(639): Show |
1 | a0002c0008t0004g0025 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(648): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(773): Show |
1 | a0001c0002t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(782): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTGGG others(1114): Show |
1 | a0003c0014t0001g0310 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1123): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(5): Show |
32 | a0001c0001t0001g0148 a0001c0001t0002g0115 a0001c0001t0002g0116 others(29): Show |
34 | HG00099.hp1 HG00280.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(37): Show |
1 | a0001c0001t0002g0122 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(325): Show |
1 | a0001c0001t0002g0123 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(334): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(389): Show |
1 | a0001c0001t0002g0124 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(398): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(165): Show |
1 | a0001c0003t0002g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(174): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(677): Show |
1 | a0001c0002t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(686): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(101): Show |
1 | a0001c0012t0001g0076 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(110): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(37): Show |
1 | a0001c0002t0013g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(366): Show |
1 | a0001c0001t0001g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(375): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(69): Show |
1 | a0001c0032t0002g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(37): Show |
2 | a0001c0002t0001g0085 a0001c0003t0002g0314 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(165): Show |
1 | a0001c0018t0001g0034 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(174): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(69): Show |
1 | a0001c0009t0005g0118 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(421): Show |
1 | a0001c0002t0001g0043 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(430): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(325): Show |
1 | a0001c0002t0001g0110 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(334): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(357): Show |
1 | a0001c0002t0001g0078 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(366): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(69): Show |
1 | a0001c0001t0002g0142 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(133): Show |
1 | a0003c0027t0001g0109 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(142): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1231): Show |
1 | a0001c0003t0003g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1240): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(505): Show |
1 | a0001c0003t0003g0286 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(514): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(569): Show |
1 | a0001c0003t0003g0287 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(578): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(569): Show |
2 | a0001c0003t0003g0278 a0001c0003t0016g0279 |
2 | NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(578): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(229): Show |
1 | a0001c0002t0001g0065 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(238): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(687): Show |
1 | a0001c0003t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(696): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(821): Show |
1 | a0001c0001t0021g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(830): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(622): Show |
1 | a0001c0003t0003g0291 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(631): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(666): Show |
1 | a0001c0003t0003g0232 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(675): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(592): Show |
1 | a0001c0003t0008g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(601): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(175): Show |
1 | a0001c0003t0014g0233 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(184): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(90): Show |
2 | a0001c0003t0003g0282 a0001c0003t0014g0264 |
2 | HG02040.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(99): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(122): Show |
1 | a0001c0003t0003g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(131): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(613): Show |
1 | a0001c0003t0003g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(622): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(165): Show |
1 | a0001c0002t0001g0047 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(174): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(37): Show |
2 | a0001c0005t0001g0203 a0002c0008t0004g0135 |
2 | HG03139.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(69): Show |
2 | a0001c0001t0002g0298 a0001c0009t0005g0113 |
2 | HG02056.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(78): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(101): Show |
1 | a0001c0001t0002g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(110): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(687): Show |
2 | a0001c0003t0003g0223 a0001c0003t0003g0228 |
2 | NA18975.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(696): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(815): Show |
1 | a0001c0003t0003g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(824): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1124): Show |
1 | a0001c0003t0003g0285 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1133): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(165): Show |
1 | a0001c0002t0002g0090 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(174): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(197): Show |
1 | a0001c0002t0002g0091 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(206): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1017): Show |
1 | a0001c0003t0003g0265 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1026): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(687): Show |
1 | a0001c0003t0003g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(696): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(687): Show |
1 | a0001c0003t0003g0227 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(696): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(687): Show |
2 | a0001c0003t0003g0258 a0001c0003t0003g0275 |
2 | HG02027.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(696): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(197): Show |
1 | a0001c0001t0002g0189 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(206): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(953): Show |
1 | a0001c0003t0006g0267 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(962): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(645): Show |
1 | a0001c0003t0003g0226 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(654): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(591): Show |
1 | a0001c0003t0008g0254 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(600): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(495): Show |
1 | a0001c0003t0003g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(504): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(559): Show |
1 | a0001c0003t0003g0230 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(568): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1199): Show |
1 | a0001c0003t0003g0263 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1208): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1263): Show |
1 | a0001c0003t0008g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1272): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(314): Show |
1 | a0001c0003t0003g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(323): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(1263): Show |
1 | a0001c0003t0003g0257 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(1272): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(463): Show |
1 | a0001c0003t0002g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(472): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(527): Show |
1 | a0001c0003t0006g0222 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(536): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(5): Show |
1 | a0001c0002t0001g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTCG others(229): Show |
1 | a0001c0003t0002g0313 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2182+158_2182+159i others(238): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTTG others(5): Show |
2 | a0001c0002t0001g0039 a0001c0022t0001g0087 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2182+158_2182+159i others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | CGGGTTTG others(111): Show |
1 | a0001c0002t0001g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2182+158_2182+159i others(120): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917219 | C | T | 1 | a0001c0001t0002g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2182+157C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917219 | |||||||
chr12:131917219 | CGAGGCTG others(25): Show |
C | 1 | a0001c0002t0002g0311 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2183-140_2183-109d others(34): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917219 | ||||||
chr12:131917225 | T | C | 3 | a0001c0003t0012g0302 a0001c0013t0012g0303 a0007c0015t0001g0219 |
3 | HG01891.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182+163T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917225 | |||||||
chr12:131917232 | C | CGGGGGTC others(25): Show |
1 | a0001c0001t0026g0297 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2183-148_2183-147i others(34): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917232 | ||||||
chr12:131917232 | C | T | 138 | a0001c0001t0001g0009 a0001c0001t0001g0134 a0001c0001t0001g0148 others(135): Show |
144 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2182+170C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917232 | |||||||
chr12:131917233 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2182+171G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917233 | |||||||
chr12:131917234 | GGGGTCGG others(4): Show |
G | 9 | a0001c0002t0001g0059 a0001c0002t0001g0096 a0001c0005t0001g0151 others(6): Show |
9 | HG01255.hp1 HG02004.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.2183-174_2183-164d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917234 | ||||||
chr12:131917236 | G | GCTCGGAG others(3): Show |
3 | a0002c0004t0004g0017 a0002c0004t0004g0157 a0002c0004t0022g0153 |
3 | HG03017.hp2 HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2182+174_2183-174i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917236 | |||||||
chr12:131917236 | G | GCTCGGAG others(129): Show |
1 | a0002c0004t0004g0141 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2182+174_2183-174i others(138): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917236 | |||||||
chr12:131917237 | G | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0147 |
2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2183-174G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917237 | |||||||
chr12:131917237 | GTCGGGTT others(4): Show |
G | 8 | a0001c0001t0007g0205 a0001c0002t0001g0002 a0001c0002t0001g0041 others(5): Show |
10 | HG01515.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2183-169_2183-159d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917237 | ||||||
chr12:131917239 | C | CGGAGGCT others(3): Show |
3 | a0001c0006t0004g0181 a0002c0004t0004g0022 a0002c0004t0004g0269 |
3 | HG02965.hp2 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2183-170_2183-169i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | CGGAGGCT others(696): Show |
1 | a0002c0033t0002g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2183-170_2183-169i others(705): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | CGGAGGCT others(161): Show |
1 | a0001c0001t0002g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2183-170_2183-169i others(170): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | CGGAGGCT others(45): Show |
2 | a0001c0006t0004g0268 a0002c0004t0023g0145 |
2 | HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2183-170_2183-169i others(54): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | CGGAGGCT others(379): Show |
1 | a0002c0004t0004g0023 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2183-170_2183-169i others(388): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | CGGAGGCT others(150): Show |
1 | a0001c0001t0002g0011 | 2 | NA18940.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.2183-170_2183-169i others(159): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917239 | C | G | 4 | a0002c0004t0004g0017 a0002c0004t0004g0141 a0002c0004t0004g0157 others(1): Show |
4 | HG02027.hp2 HG03017.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-172C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917239 | |||||||
chr12:131917239 | CGGGTTCG others(5): Show |
C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0147 |
2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2183-170_2183-159d others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917239 | ||||||
chr12:131917242 | G | A | 15 | a0001c0001t0002g0011 a0001c0001t0002g0137 a0001c0001t0002g0166 others(12): Show |
16 | HG01516.hp1 HG02027.hp2 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.2183-169G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917242 | |||||||
chr12:131917242 | G | GGGCTGTG others(3): Show |
1 | a0002c0004t0004g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2183-169_2183-168i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917242 | |||||||
chr12:131917242 | G | GTGGGGCT others(109): Show |
1 | a0001c0002t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2183-168_2183-167i others(118): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917242 | ||||||
chr12:131917243 | T | G | 4 | a0001c0001t0002g0010 a0001c0001t0002g0137 a0001c0021t0003g0309 others(1): Show |
5 | HG01168.hp1 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2183-168T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917243 | |||||||
chr12:131917244 | T | G | 60 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0125 others(57): Show |
62 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.2183-167T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917244 | |||||||
chr12:131917245 | C | CGGCTCGG others(67): Show |
2 | a0001c0001t0001g0201 a0001c0001t0002g0167 |
2 | HG00099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2183-148_2183-147i others(76): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917245 | ||||||
chr12:131917245 | C | CGGCTCGG others(173): Show |
1 | a0001c0001t0002g0206 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(182): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917245 | ||||||
chr12:131917245 | C | CGGCTCGG others(35): Show |
1 | a0001c0002t0004g0082 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2183-148_2183-147i others(44): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917245 | ||||||
chr12:131917245 | C | CTGTGGGA others(3): Show |
1 | a0001c0021t0003g0309 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2183-166_2183-165i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917245 | |||||||
chr12:131917245 | C | CTGTGGGA others(192): Show |
1 | a0001c0001t0002g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2183-166_2183-165i others(201): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917245 | |||||||
chr12:131917245 | C | G | 58 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0125 others(55): Show |
60 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.2183-166C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917245 | |||||||
chr12:131917246 | G | A | 2 | a0001c0001t0002g0010 a0002c0004t0004g0019 |
3 | HG01168.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.2183-165G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917246 | |||||||
chr12:131917246 | G | GGCTCGGA others(774): Show |
1 | a0002c0004t0004g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2183-148_2183-147i others(783): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917246 | ||||||
chr12:131917246 | G | GGCTTGGA others(25): Show |
1 | a0001c0002t0002g0316 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2183-162_2183-161i others(34): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917246 | ||||||
chr12:131917248 | C | CTCGGAGG others(109): Show |
1 | a0001c0001t0002g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2183-116_2183-115i others(118): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917248 | ||||||
chr12:131917248 | C | CTCGGAGG others(14): Show |
1 | a0002c0008t0025g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(23): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917248 | ||||||
chr12:131917248 | C | G | 9 | a0001c0001t0002g0137 a0001c0006t0004g0268 a0001c0021t0003g0309 others(6): Show |
9 | HG02027.hp2 HG02257.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2183-163C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917248 | |||||||
chr12:131917250 | C | T | 14 | a0001c0002t0001g0032 a0001c0002t0001g0039 a0001c0002t0001g0047 others(11): Show |
14 | HG01106.hp1 HG01891.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.2183-161C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917250 | |||||||
chr12:131917250 | CG | C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0002g0166 others(3): Show |
7 | HG01516.hp1 HG03540.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.2183-159delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917250 | ||||||
chr12:131917250 | CGGAGGCT others(58): Show |
C | 2 | a0001c0002t0001g0033 a0001c0002t0001g0061 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2183-159_2183-95de others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917250 | ||||||
chr12:131917251 | G | GGAGGCTG others(108): Show |
1 | a0001c0001t0003g0162 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2183-116_2183-115i others(117): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(1086): Show |
1 | a0001c0006t0028g0184 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2183-148_2183-147i others(1095): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(139): Show |
1 | a0001c0001t0002g0200 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2183-148_2183-147i others(148): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(97): Show |
1 | a0002c0008t0004g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(106): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(76): Show |
2 | a0001c0001t0002g0194 a0001c0001t0007g0159 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2183-148_2183-147i others(85): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(182): Show |
1 | a0001c0001t0002g0300 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(191): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(55): Show |
1 | a0002c0004t0004g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917251 | G | GGAGGCTG others(118): Show |
1 | a0002c0004t0004g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2183-148_2183-147i others(127): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917251 | ||||||
chr12:131917257 | T | C | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2183-154T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917257 | |||||||
chr12:131917257 | TGTGGGAC others(57): Show |
T | 2 | a0001c0003t0009g0005 a0001c0005t0001g0158 |
4 | NA18947.hp2 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183-147_2183-84de others(65): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917257 | ||||||
chr12:131917264 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(131): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.2183-147C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917264 | |||||||
chr12:131917266 | GGGGTCGG others(4): Show |
G | 1 | a0001c0002t0001g0057 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2183-142_2183-132d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917266 | ||||||
chr12:131917268 | G | GCTCGGAG others(108): Show |
2 | a0001c0001t0002g0140 a0001c0001t0002g0168 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2183-143_2183-142i others(117): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917268 | |||||||
chr12:131917269 | G | C | 1 | a0006c0036t0004g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2183-142G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917269 | |||||||
chr12:131917269 | GTCGGGTT others(4): Show |
G | 2 | a0001c0002t0001g0002 a0001c0005t0001g0301 |
4 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-137_2183-127d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917269 | ||||||
chr12:131917271 | C | CGGAGGCT others(3): Show |
15 | a0001c0001t0002g0137 a0001c0001t0007g0205 a0001c0002t0001g0041 others(12): Show |
15 | HG02027.hp2 HG02647.hp1 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.2183-138_2183-137i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | CGGAGGCT others(380): Show |
1 | a0001c0006t0004g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2183-138_2183-137i others(389): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | CGGAGGCT others(23): Show |
1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2183-138_2183-137i others(32): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | CGGAGGCT others(24): Show |
1 | a0002c0004t0004g0269 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2183-138_2183-137i others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | CGGAGGCT others(87): Show |
1 | a0002c0004t0004g0017 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2183-138_2183-137i others(96): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | CGGAGGCT others(4864): Show |
1 | a0002c0004t0004g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2183-138_2183-137i others(4873): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917271 | C | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0168 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.2183-140C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917271 | |||||||
chr12:131917271 | CGGGTTCG others(5): Show |
C | 1 | a0006c0036t0004g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2183-138_2183-127d others(14): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917271 | ||||||
chr12:131917272 | G | A | 6 | a0001c0001t0002g0160 a0001c0006t0004g0149 a0001c0010t0002g0209 others(3): Show |
6 | HG01071.hp2 HG01106.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183-139G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917272 | |||||||
chr12:131917274 | G | A | 20 | a0001c0001t0002g0137 a0001c0001t0002g0140 a0001c0001t0002g0168 others(17): Show |
20 | HG00280.hp2 HG01074.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.2183-137G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917274 | |||||||
chr12:131917274 | G | GGGCTGTG others(3): Show |
1 | a0002c0004t0004g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-137_2183-136i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917274 | |||||||
chr12:131917275 | T | A | 1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2183-136T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917275 | |||||||
chr12:131917275 | T | G | 3 | a0001c0001t0002g0010 a0002c0004t0004g0020 a0002c0004t0004g0021 |
4 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183-136T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917275 | |||||||
chr12:131917276 | T | A | 1 | a0001c0002t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2183-135T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917276 | |||||||
chr12:131917276 | T | G | 39 | a0001c0001t0002g0010 a0001c0001t0002g0124 a0001c0001t0002g0137 others(36): Show |
41 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.2183-135T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917276 | |||||||
chr12:131917277 | C | CGGCTCGG others(226): Show |
1 | a0001c0002t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2183-116_2183-115i others(235): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917277 | ||||||
chr12:131917277 | C | G | 41 | a0001c0001t0002g0010 a0001c0001t0002g0124 a0001c0001t0002g0137 others(38): Show |
43 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.2183-134C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917277 | |||||||
chr12:131917278 | G | A | 3 | a0001c0001t0002g0010 a0002c0004t0004g0020 a0002c0033t0002g0216 |
4 | HG01168.hp1 HG01169.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-133G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917278 | |||||||
chr12:131917280 | C | CTCGAGGC others(358): Show |
1 | a0002c0008t0004g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2183-128_2183-127i others(367): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917280 | ||||||
chr12:131917280 | C | CTCGGAGG others(1001): Show |
1 | a0001c0001t0002g0160 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2183-116_2183-115i others(1010): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917280 | ||||||
chr12:131917280 | C | G | 6 | a0001c0001t0002g0137 a0001c0002t0001g0059 a0001c0006t0004g0276 others(3): Show |
6 | HG01074.hp2 HG02055.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2183-131C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917280 | |||||||
chr12:131917282 | C | CGGAGGCT others(1013): Show |
1 | a0001c0003t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2183-109_2183-108i others(1022): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917282 | ||||||
chr12:131917282 | C | T | 9 | a0001c0001t0002g0124 a0001c0002t0001g0053 a0001c0002t0001g0068 others(6): Show |
9 | HG01928.hp1 HG02080.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.2183-129C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917282 | |||||||
chr12:131917282 | CG | C | 9 | a0001c0001t0002g0140 a0001c0001t0002g0168 a0001c0006t0004g0181 others(6): Show |
9 | HG00280.hp2 HG02027.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2183-127delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917282 | ||||||
chr12:131917283 | G | A | 1 | a0001c0002t0001g0097 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2183-128G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917283 | |||||||
chr12:131917283 | G | GGAGGCTG others(13): Show |
6 | a0001c0001t0001g0201 a0001c0001t0002g0137 a0001c0001t0002g0167 others(3): Show |
6 | HG00099.hp2 HG02818.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183-116_2183-115i others(22): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(139): Show |
1 | a0002c0008t0004g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2183-116_2183-115i others(148): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(55): Show |
1 | a0001c0001t0015g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2183-116_2183-115i others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(991): Show |
1 | a0002c0004t0004g0012 | 2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2183-116_2183-115i others(1000): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(97): Show |
1 | a0002c0004t0004g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2183-116_2183-115i others(106): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(923): Show |
1 | a0005c0034t0004g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2183-116_2183-115i others(932): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(1325): Show |
1 | a0001c0006t0004g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2183-116_2183-115i others(1334): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917283 | G | GGAGGCTG others(1384): Show |
1 | a0001c0001t0002g0274 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2183-116_2183-115i others(1393): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917283 | ||||||
chr12:131917289 | T | C | 1 | a0001c0003t0012g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2183-122T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917289 | |||||||
chr12:131917289 | TGTGGGAC others(25): Show |
T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0318 others(15): Show |
22 | HG01099.hp1 HG01192.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.2183-115_2183-84de others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917289 | ||||||
chr12:131917296 | C | CGGGGGTC others(57): Show |
1 | a0001c0002t0001g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2183-109_2183-108i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917296 | ||||||
chr12:131917296 | C | CGGGGGTC others(441): Show |
1 | a0001c0002t0001g0063 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2183-109_2183-108i others(450): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917296 | ||||||
chr12:131917296 | C | T | 146 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(143): Show |
153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.2183-115C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917296 | |||||||
chr12:131917298 | G | GGGCTCGG others(7): Show |
2 | a0001c0002t0001g0002 a0001c0002t0001g0059 |
4 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-111_2183-110i others(16): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917298 | ||||||
chr12:131917299 | GGGTTGGG others(4): Show |
G | 1 | a0001c0005t0001g0301 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2183-110_2183-100d others(13): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917299 | ||||||
chr12:131917302 | T | A | 2 | a0001c0002t0001g0002 a0001c0002t0001g0059 |
4 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-109T>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917302 | |||||||
chr12:131917303 | T | C | 291 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(288): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2183-108T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917303 | |||||||
chr12:131917305 | G | GTTCGGCT others(650): Show |
1 | a0001c0001t0002g0187 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2183-106_2183-105i others(659): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917305 | |||||||
chr12:131917306 | G | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0126 a0001c0001t0002g0150 others(15): Show |
19 | HG00140.hp1 HG00408.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2183-105G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(118): Show |
1 | a0001c0006t0003g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(127): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(96): Show |
1 | a0001c0002t0001g0105 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(105): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(86): Show |
1 | a0001c0001t0002g0125 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(95): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(1750): Show |
1 | a0001c0002t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(1759): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(2262): Show |
1 | a0001c0001t0002g0114 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(2271): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(214): Show |
1 | a0001c0020t0003g0251 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(223): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(118): Show |
1 | a0001c0003t0003g0261 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(127): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(618): Show |
1 | a0011c0037t0003g0280 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(627): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(2224): Show |
1 | a0001c0001t0002g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(2233): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(22): Show |
9 | a0001c0001t0001g0182 a0001c0001t0002g0300 a0001c0002t0001g0086 others(6): Show |
9 | HG01884.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2183-105_2183-104i others(31): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(557): Show |
1 | a0010c0028t0002g0308 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(566): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(367): Show |
1 | a0001c0001t0002g0273 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(376): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(95): Show |
2 | a0002c0008t0004g0130 a0002c0008t0004g0131 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2183-105_2183-104i others(104): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(342): Show |
1 | a0004c0016t0013g0073 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(351): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(99): Show |
1 | a0002c0004t0004g0030 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(108): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(214): Show |
1 | a0001c0019t0001g0081 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(223): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(150): Show |
1 | a0001c0003t0003g0288 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(159): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(1492): Show |
1 | a0001c0003t0003g0237 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(1501): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(54): Show |
2 | a0001c0002t0001g0079 a0001c0003t0003g0260 |
2 | HG01981.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2183-105_2183-104i others(63): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(158): Show |
1 | a0001c0006t0004g0186 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(167): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(1096): Show |
1 | a0001c0003t0003g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(1105): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(1236): Show |
1 | a0001c0003t0003g0250 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(1245): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(928): Show |
1 | a0001c0003t0024g0283 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2183-105_2183-104i others(937): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(685): Show |
1 | a0001c0003t0003g0245 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(694): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917306 | G | GTTCGGCT others(749): Show |
1 | a0001c0003t0003g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2183-105_2183-104i others(758): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917306 | |||||||
chr12:131917307 | G | GGCTGTGG others(3): Show |
6 | a0001c0001t0002g0004 a0001c0001t0002g0126 a0001c0001t0002g0150 others(3): Show |
7 | HG00735.hp1 HG02257.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2183-103_2183-102i others(12): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917307 | ||||||
chr12:131917307 | G | GGCTGTGG others(24): Show |
1 | a0002c0004t0004g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2183-103_2183-102i others(33): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917307 | ||||||
chr12:131917307 | G | GGCTGTGG others(66): Show |
1 | a0002c0004t0004g0133 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2183-103_2183-102i others(75): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917307 | ||||||
chr12:131917307 | G | GGCTGTGG others(875): Show |
1 | a0002c0004t0004g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(884): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917307 | ||||||
chr12:131917307 | G | T | 233 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2183-104G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917307 | |||||||
chr12:131917308 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2183-103G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(1812): Show |
1 | a0001c0030t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(1821): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(244): Show |
1 | a0002c0004t0002g0172 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2183-103_2183-102i others(253): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(2211): Show |
1 | a0001c0010t0002g0218 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(2220): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(812): Show |
1 | a0001c0010t0002g0209 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(821): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(1735): Show |
1 | a0001c0001t0002g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(1744): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(1368): Show |
1 | a0001c0010t0004g0208 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(1377): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(572): Show |
1 | a0001c0006t0002g0277 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(581): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(76): Show |
1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(85): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GCTGTGGG others(110): Show |
1 | a0001c0003t0006g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2183-103_2183-102i others(119): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | GTCGGGTT | 2 | a0001c0002t0001g0002 a0001c0002t0001g0059 |
4 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-103_2183-102i others(9): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917308 | G | T | 178 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(175): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2183-103G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917308 | |||||||
chr12:131917309 | G | C | 191 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(188): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.2183-102G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCAG others(313): Show |
1 | a0001c0002t0001g0088 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(322): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(1945): Show |
1 | a0001c0002t0001g0083 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(1954): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(345): Show |
1 | a0001c0002t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(354): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(57): Show |
1 | a0001c0002t0001g0036 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(237): Show |
1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(246): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(1145): Show |
1 | a0001c0002t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(1154): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTCGG others(747): Show |
1 | a0002c0031t0002g0198 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(756): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(408): Show |
1 | a0001c0023t0003g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(417): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(419): Show |
1 | a0001c0002t0001g0307 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(428): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(345): Show |
1 | a0001c0002t0001g0044 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(354): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(908): Show |
1 | a0001c0010t0002g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(917): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(57): Show |
2 | a0001c0002t0001g0075 a0001c0002t0013g0074 |
2 | HG02083.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2183-102_2183-101i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(25): Show |
1 | a0001c0002t0001g0085 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(34): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGCTTGG others(57): Show |
1 | a0001c0001t0002g0122 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2183-102_2183-101i others(66): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GGGGTCGG others(1122): Show |
1 | a0002c0004t0004g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2183-102_2183-101i others(1131): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917309 | G | GTTC | 31 | a0001c0001t0001g0182 a0001c0001t0002g0114 a0001c0001t0002g0117 others(28): Show |
31 | HG00280.hp1 HG00597.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.2183-102_2183-101i others(5): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917309 | |||||||
chr12:131917310 | A | AGCTCGGA others(121): Show |
1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(128): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917310 | ||||||
chr12:131917310 | A | AGCTCGGA others(87): Show |
1 | a0001c0001t0002g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2183-91_2183-90ins others(94): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917310 | ||||||
chr12:131917310 | A | AGCTCGGA others(1734): Show |
1 | a0002c0004t0004g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(1741): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917310 | ||||||
chr12:131917310 | A | G | 285 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(282): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2183-101A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917310 | |||||||
chr12:131917314 | C | T | 15 | a0001c0002t0001g0032 a0001c0002t0001g0042 a0001c0002t0001g0062 others(12): Show |
15 | HG01106.hp1 HG01261.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2183-97C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917314 | |||||||
chr12:131917314 | CG | C | 8 | a0001c0001t0002g0004 a0001c0001t0002g0126 a0001c0001t0002g0150 others(5): Show |
9 | HG00735.hp1 HG02293.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2183-95delG | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917314 | ||||||
chr12:131917315 | G | GGAGGCTG others(2239): Show |
1 | a0001c0002t0001g0100 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(2246): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(567): Show |
1 | a0001c0002t0001g0102 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(574): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(1065): Show |
1 | a0001c0002t0001g0235 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(1072): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(183): Show |
1 | a0008c0026t0001g0099 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(190): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(119): Show |
1 | a0001c0002t0011g0038 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(126): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(468): Show |
1 | a0001c0002t0001g0243 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(475): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(2335): Show |
1 | a0001c0002t0001g0098 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(2342): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917315 | G | GGAGGCTG others(5569): Show |
1 | a0001c0002t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2183-91_2183-90ins others(5576): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917315 | ||||||
chr12:131917321 | C | CGTGGGAT others(57): Show |
1 | a0001c0003t0012g0302 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2183-42_2183-41ins others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917321 | ||||||
chr12:131917321 | C | T | 293 | a0001c0001t0001g0009 a0001c0001t0001g0127 a0001c0001t0001g0128 others(290): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.2183-90C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917321 | |||||||
chr12:131917328 | T | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0126 a0001c0001t0002g0150 others(28): Show |
32 | HG00438.hp1 HG00735.hp1 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.2183-83T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917328 | |||||||
chr12:131917328 | T | TGGGGCTC others(244): Show |
1 | a0002c0008t0025g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2183-79_2183-78ins others(251): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(55): Show |
1 | a0001c0002t0001g0097 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2183-74_2183-73ins others(62): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(685): Show |
1 | a0002c0004t0004g0019 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2183-74_2183-73ins others(692): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(255): Show |
1 | a0002c0008t0004g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2183-72_2183-71ins others(262): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(802): Show |
1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2183-72_2183-71ins others(809): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(1206): Show |
1 | a0002c0025t0001g0080 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2183-72_2183-71ins others(1213): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(1657): Show |
1 | a0001c0003t0001g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2183-72_2183-71ins others(1664): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(3382): Show |
1 | a0001c0002t0019g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2183-72_2183-71ins others(3389): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTC others(57): Show |
2 | a0001c0002t0001g0068 a0001c0002t0001g0069 |
2 | HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.2183-72_2183-71ins others(64): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917328 | T | TGGGGGTT others(1082): Show |
1 | a0002c0004t0004g0022 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2183-77_2183-76ins others(1089): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917328 | ||||||
chr12:131917333 | G | C | 1 | a0002c0004t0004g0185 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2183-78G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917333 | |||||||
chr12:131917333 | GTCGGGTT others(4): Show |
G | 1 | a0001c0005t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2183-73_2183-63del others(11): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917333 | ||||||
chr12:131917340 | T | G | 4 | a0001c0001t0002g0142 a0001c0001t0002g0189 a0001c0002t0001g0104 others(1): Show |
4 | HG02735.hp1 NA18956.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-71T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917340 | |||||||
chr12:131917341 | C | CGGCTCGG others(121): Show |
1 | a0001c0009t0005g0118 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2183-52_2183-51ins others(128): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917341 | ||||||
chr12:131917341 | C | CGGCTCGG others(982): Show |
1 | a0001c0002t0003g0089 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2183-52_2183-51ins others(989): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917341 | ||||||
chr12:131917341 | C | G | 4 | a0001c0001t0002g0142 a0001c0001t0002g0189 a0001c0002t0001g0104 others(1): Show |
4 | HG02735.hp1 NA18956.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183-70C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917341 | |||||||
chr12:131917346 | C | CGAGGCTG others(55): Show |
1 | a0001c0001t0017g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2183-64_2183-63ins others(62): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 131917346 | ||||||
chr12:131917347 | G | A | 1 | a0001c0002t0002g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2183-64G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917347 | |||||||
chr12:131917360 | T | C | 9 | a0001c0002t0001g0039 a0001c0002t0001g0104 a0001c0002t0001g0305 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.2183-51T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917360 | |||||||
chr12:131917365 | G | A | 1 | a0001c0002t0002g0093 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2183-46G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917365 | |||||||
chr12:131917368 | G | A | 2 | a0001c0001t0002g0164 a0001c0009t0005g0113 |
2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2183-43G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 21/27 | chr12 | 131917368 | |||||||
chr12:131917612 | G | A | 3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | HG01891.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2326+58G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917612 | |||||||
chr12:131917634 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2326+80G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917634 | |||||||
chr12:131917652 | C | G | 68 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0003t0002g0244 others(65): Show |
72 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.2326+98C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917652 | |||||||
chr12:131917725 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2326+171G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917725 | |||||||
chr12:131917756 | A | G | 1 | a0001c0001t0002g0164 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2326+202A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917756 | |||||||
chr12:131917779 | G | C | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2326+225G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917779 | |||||||
chr12:131917796 | G | A | 1 | a0001c0009t0005g0018 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2326+242G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131917796 | |||||||
chr12:131918057 | T | C | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2327-440T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131918057 | |||||||
chr12:131918329 | T | G | 77 | a0001c0002t0002g0093 a0001c0002t0002g0304 a0001c0002t0002g0311 others(74): Show |
81 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2327-168T>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131918329 | |||||||
chr12:131918369 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2327-128G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 22/27 | chr12 | 131918369 | |||||||
chr12:131918722 | G | A | 2 | a0001c0003t0003g0266 a0001c0003t0006g0267 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2511+41G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918722 | |||||||
chr12:131918730 | G | GGGGTGTC others(325): Show |
1 | a0001c0003t0003g0240 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2511+55_2511+56ins others(332): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTC others(326): Show |
1 | a0001c0003t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2511+55_2511+56ins others(333): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTC others(326): Show |
1 | a0001c0003t0003g0255 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2511+55_2511+56ins others(333): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTC others(325): Show |
1 | a0001c0003t0003g0284 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2511+55_2511+56ins others(332): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTC others(325): Show |
62 | a0001c0003t0003g0014 a0001c0003t0003g0015 a0001c0003t0003g0223 others(59): Show |
66 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2511+55_2511+56ins others(332): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(472): Show |
1 | a0001c0001t0002g0122 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(479): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(487): Show |
1 | a0001c0001t0002g0166 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(494): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(471): Show |
1 | a0001c0002t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(478): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(594): Show |
1 | a0001c0001t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(601): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(593): Show |
1 | a0001c0001t0021g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(600): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(515): Show |
2 | a0002c0008t0004g0029 a0005c0034t0004g0211 |
2 | HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2511+96_2511+97ins others(522): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(487): Show |
81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(78): Show |
86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.2511+96_2511+97ins others(494): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(480): Show |
1 | a0001c0001t0002g0296 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(487): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918730 | G | GGGGTGTG others(351): Show |
10 | a0001c0002t0002g0093 a0001c0002t0002g0304 a0001c0002t0002g0311 others(7): Show |
10 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2511+96_2511+97ins others(358): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918730 | ||||||
chr12:131918734 | T | TGTCGGGT others(309): Show |
1 | a0001c0003t0002g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2511+55_2511+56ins others(316): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918734 | ||||||
chr12:131918737 | G | A | 1 | a0001c0003t0002g0244 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2511+56G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918737 | |||||||
chr12:131918738 | T | TGGGGTGT others(488): Show |
1 | a0001c0001t0002g0189 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2511+96_2511+97ins others(495): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918738 | ||||||
chr12:131918760 | A | ATAGGGTG others(9): Show |
22 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 others(19): Show |
24 | HG01074.hp1 HG01081.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2511+81_2511+96dup others(16): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918760 | ||||||
chr12:131918778 | C | A | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+97C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918778 | |||||||
chr12:131918778 | C | CGGGTGTG others(472): Show |
1 | a0001c0001t0002g0116 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2511+128_2511+129i others(481): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918778 | ||||||
chr12:131918778 | C | CGGGTGTG others(455): Show |
2 | a0001c0002t0001g0306 a0001c0002t0001g0307 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2511+128_2511+129i others(464): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918778 | ||||||
chr12:131918778 | C | CGGGTGTG others(473): Show |
1 | a0002c0011t0004g0026 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2511+128_2511+129i others(482): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918778 | ||||||
chr12:131918778 | C | CGGGTGTG others(471): Show |
17 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0164 others(14): Show |
19 | HG01074.hp1 HG01081.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2511+128_2511+129i others(480): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918778 | ||||||
chr12:131918778 | C | T | 90 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(87): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2511+97C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918778 | |||||||
chr12:131918780 | G | GGT | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+103_2511+104d others(4): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918780 | ||||||
chr12:131918784 | T | TGGGGGTG others(475): Show |
1 | a0002c0004t0004g0179 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2511+107_2511+108i others(484): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918784 | ||||||
chr12:131918794 | G | GGTGTGGG others(287): Show |
5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+114_2511+115i others(296): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918794 | ||||||
chr12:131918801 | G | GGGGTGTA others(455): Show |
1 | a0001c0001t0002g0298 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2511+128_2511+129i others(464): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918801 | ||||||
chr12:131918861 | C | T | 2 | a0001c0021t0003g0309 a0010c0028t0002g0308 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2511+180C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918861 | |||||||
chr12:131918877 | C | G | 3 | a0001c0001t0002g0142 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | NA18944.hp1 NA18956.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2511+196C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918877 | |||||||
chr12:131918881 | T | TGTGTGGG | 301 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(298): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2511+205_2511+211d others(9): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918881 | ||||||
chr12:131918881 | T | TGTGTGGG others(16): Show |
1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2511+211_2511+212i others(25): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918881 | ||||||
chr12:131918881 | T | TGTGTGGG others(37): Show |
7 | a0001c0002t0002g0093 a0001c0002t0002g0304 a0001c0002t0002g0311 others(4): Show |
7 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2511+211_2511+212i others(46): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918881 | ||||||
chr12:131918886 | GGGGTGTA | G | 5 | a0001c0001t0002g0142 a0001c0001t0002g0190 a0001c0003t0003g0287 others(2): Show |
5 | NA18944.hp1 NA18956.hp2 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+212_2511+218d others(9): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918886 | ||||||
chr12:131918893 | A | G | 6 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0001c0002t0001g0106 others(3): Show |
6 | HG00408.hp2 HG01243.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.2511+212A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918893 | |||||||
chr12:131918899 | T | TAGGGTGT others(17): Show |
1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2511+218_2511+219i others(26): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918899 | |||||||
chr12:131918900 | G | A | 3 | a0001c0003t0002g0054 a0001c0003t0002g0312 a0001c0003t0002g0315 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2511+219G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918900 | |||||||
chr12:131918906 | T | C | 3 | a0001c0001t0002g0189 a0001c0001t0002g0193 a0002c0004t0004g0185 |
3 | HG00408.hp2 NA18959.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2511+225T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918906 | |||||||
chr12:131918906 | T | TAGGGTGT others(9): Show |
3 | a0001c0002t0001g0305 a0001c0002t0001g0306 a0001c0002t0001g0307 |
3 | HG01891.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2511+239_2511+240i others(18): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918906 | ||||||
chr12:131918906 | T | TAGGGTGT others(9): Show |
165 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(162): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.2512-265_2512-250d others(18): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918906 | ||||||
chr12:131918906 | T | TAGGGTGT others(8): Show |
1 | a0001c0003t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2511+237_2511+238i others(17): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918906 | ||||||
chr12:131918907 | A | C | 7 | a0001c0002t0002g0093 a0001c0002t0002g0304 a0001c0002t0002g0311 others(4): Show |
7 | HG00733.hp1 HG01175.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.2511+226A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918907 | |||||||
chr12:131918907 | A | G | 3 | a0001c0003t0002g0054 a0001c0003t0002g0312 a0001c0003t0002g0315 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2511+226A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918907 | |||||||
chr12:131918911 | T | TGTAGAGT others(21): Show |
3 | a0001c0003t0002g0054 a0001c0003t0002g0312 a0001c0003t0002g0315 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2511+232_2511+233i others(30): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918911 | ||||||
chr12:131918921 | G | A | 1 | a0001c0003t0018g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2511+240G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918921 | |||||||
chr12:131918922 | C | T | 5 | a0001c0003t0002g0054 a0001c0003t0002g0312 a0001c0003t0002g0315 others(2): Show |
5 | HG03041.hp2 HG03098.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2511+241C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918922 | |||||||
chr12:131918923 | A | AGGGTGTG others(8): Show |
1 | a0001c0001t0002g0273 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2511+243_2511+257d others(17): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918923 | ||||||
chr12:131918923 | A | C | 3 | a0001c0003t0002g0054 a0001c0003t0002g0312 a0001c0003t0002g0315 |
3 | HG03041.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2511+242A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918923 | |||||||
chr12:131918937 | G | A | 25 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0043 others(22): Show |
25 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.2511+256G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918937 | |||||||
chr12:131918938 | C | T | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+257C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918938 | |||||||
chr12:131918940 | G | C | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2511+259G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918940 | |||||||
chr12:131918948 | G | GGGGTGCA others(8): Show |
1 | a0001c0003t0003g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2512-250_2512-249i others(17): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr12 | 131918948 | ||||||
chr12:131918953 | G | A | 6 | a0001c0007t0001g0006 a0001c0007t0001g0007 a0001c0007t0001g0052 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2512-259G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918953 | |||||||
chr12:131918968 | C | T | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512-244C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918968 | |||||||
chr12:131918969 | A | C | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512-243A>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918969 | |||||||
chr12:131918972 | G | C | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512-240G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918972 | |||||||
chr12:131918984 | T | C | 2 | a0001c0003t0003g0287 a0001c0003t0016g0279 |
2 | NA19062.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2512-228T>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918984 | |||||||
chr12:131918985 | C | A | 7 | a0001c0003t0003g0287 a0001c0003t0016g0279 a0001c0009t0005g0018 others(4): Show |
7 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.2512-227C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918985 | |||||||
chr12:131918986 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2512-226G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918986 | |||||||
chr12:131918986 | G | C | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512-226G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131918986 | |||||||
chr12:131919045 | G | A | 1 | a0001c0003t0003g0227 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2512-167G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131919045 | |||||||
chr12:131919150 | A | G | 1 | a0001c0002t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2512-62A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 23/27 | chr12 | 131919150 | |||||||
chr12:131919427 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2684+43G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 24/27 | chr12 | 131919427 | |||||||
chr12:131919692 | C | G | 2 | a0001c0003t0003g0266 a0001c0003t0006g0267 |
2 | NA18971.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2803+102C>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | chr12 | 131919692 | |||||||
chr12:131919714 | C | T | 307 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(304): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.2803+124C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | chr12 | 131919714 | |||||||
chr12:131919723 | GGCCCAGT others(41): Show |
G | 3 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 |
3 | HG01928.hp1 HG01978.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2803+141_2803+188d others(50): Show |
ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr12 | 131919723 | ||||||
chr12:131919761 | A | G | 3 | a0001c0002t0001g0033 a0001c0002t0001g0061 a0007c0015t0001g0219 |
3 | HG01891.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2803+171A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | chr12 | 131919761 | |||||||
chr12:131919816 | G | A | 2 | a0001c0002t0001g0044 a0001c0021t0003g0309 |
2 | HG02647.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.2804-163G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | chr12 | 131919816 | |||||||
chr12:131919967 | C | T | 3 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0108 |
3 | HG01175.hp1 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2804-12C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 25/27 | chr12 | 131919967 | |||||||
chr12:131920187 | C | T | 1 | a0007c0015t0001g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2961+51C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920187 | |||||||
chr12:131920205 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2961+69G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920205 | |||||||
chr12:131920343 | G | A | 1 | a0001c0001t0026g0297 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2961+207G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920343 | |||||||
chr12:131920500 | G | A | 2 | a0001c0003t0012g0302 a0001c0013t0012g0303 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2961+364G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920500 | |||||||
chr12:131920579 | G | GT | 84 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0002g0122 others(81): Show |
86 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.2961+452dupT | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 131920579 | ||||||
chr12:131920653 | A | G | 214 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0002g0003 others(211): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2962-447A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920653 | |||||||
chr12:131920665 | C | A | 199 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0010 others(196): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2962-435C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920665 | |||||||
chr12:131920685 | G | A | 3 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 |
3 | HG02109.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2962-415G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920685 | |||||||
chr12:131920710 | G | GT | 8 | a0001c0002t0001g0098 a0001c0002t0001g0100 a0001c0002t0001g0101 others(5): Show |
8 | HG01123.hp1 HG01167.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-389dupT | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr12 | 131920710 | ||||||
chr12:131920801 | C | A | 1 | a0001c0003t0003g0284 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2962-299C>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920801 | |||||||
chr12:131920876 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0016 others(48): Show |
60 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(57): Show |
intron_variant | MODIFIER | c.2962-224C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920876 | |||||||
chr12:131920888 | G | T | 61 | a0001c0002t0001g0008 a0001c0002t0001g0032 a0001c0002t0001g0033 others(58): Show |
62 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2962-212G>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920888 | |||||||
chr12:131920962 | C | T | 1 | a0001c0002t0001g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2962-138C>T | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131920962 | |||||||
chr12:131921002 | A | G | 1 | a0001c0009t0005g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2962-98A>G | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 26/27 | chr12 | 131921002 | |||||||
chr12:131921255 | G | C | 1 | a0001c0005t0001g0173 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3097+20G>C | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 27/27 | chr12 | 131921255 | |||||||
chr12:131921275 | G | A | 5 | a0001c0009t0005g0018 a0001c0009t0005g0113 a0001c0009t0005g0118 others(2): Show |
5 | HG02056.hp1 HG02735.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.3098-31G>A | ULK1 | ENSG00000177169.10 | transcript | ENST00000321867.6 | protein_coding | 27/27 | chr12 | 131921275 |