Item | Value |
---|---|
geneid | 57180 |
ensemblid | ENSG00000133627.18 |
hgncid | 17256 |
symbol | ACTR3B |
name | actin related protein 3B |
refseq_nuc | NM_020445.6 |
refseq_prot | NP_065178.1 |
ensembl_nuc | ENST00000256001.13 |
ensembl_prot | ENSP00000256001.8 |
mane_status | MANE Select |
chr | chr7 |
start | 152759752 |
end | 152855378 |
strand | + |
ver | v1.2 |
region | chr7:152759752-152855378 |
region5000 | chr7:152754752-152860378 |
regionname0 | ACTR3B_chr7_152759752_152855378 |
regionname5000 | ACTR3B_chr7_152754752_152860378 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 418 | 309 | 90 | 56 | 119 | 10 | 32 | 89 | ACTR3B_chr7_152754752_152860378 | ACTR3B | MAGSL others(413): Show |
chr7 | 152754752 | 152860378 |
a0002 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | MAGSL others(413): Show |
chr7 | 152754752 | 152860378 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1254 | 303 | 85 | 55 | 119 | 10 | 32 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0001c0002 | 0/0 | 1254 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0001c0003 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0001c0004 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0001c0005 | 0/0 | 1254 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0001c0007 | 0/0 | 1254 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 | ||
a0002c0006 | 0/0 | 1254 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATGGC others(1249): Show |
chr7 | 152754752 | 152860378 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2213 | 173 | 47 | 38 | 59 | 7 | 20 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0002 | 0/0 | 2213 | 110 | 25 | 14 | 56 | 3 | 12 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0003 | 0/0 | 2213 | 7 | 7 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0004 | 0/0 | 2213 | 3 | 3 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0005 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0006 | 0/0 | 2213 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0007 | 0/0 | 2213 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0008 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0009 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0010 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0001t0011 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0002t0001 | 0/0 | 2213 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0003t0003 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0004t0001 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0005t0001 | 0/0 | 2213 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0001c0007t0001 | 0/0 | 2213 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
a0002c0006t0001 | 0/0 | 2213 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | ATCCG others(2208): Show |
chr7 | 152754752 | 152860378 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0218 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0007g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0009g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0010g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0001t0011g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0003t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0005t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0001c0007t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
a0002c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | GBR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01099 | hp1 | a0001 | c0001 | t0011 | g0166 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0208 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01192 | hp2 | a0001 | c0007 | t0001 | g0111 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0143 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CDX | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02257 | hp1 | a0001 | c0004 | t0001 | g0301 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0169 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18948 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18984 | hp2 | a0002 | c0006 | t0001 | g0274 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19010 | hp2 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19012 | hp1 | a0001 | c0001 | t0007 | g0043 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | YRI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ASW | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ASW | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20300 | hp1 | a0001 | c0005 | t0001 | g0299 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | USA | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0218 | REF | REF | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0146 | REF | REF | ACTR3B_chr7_152754752_152860378 | ACTR3B | chr7 | 152754752 | 152860378 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:152823436 | A | G | 1 | a0002 | 1 | NA18984.hp2 | missense_variant | MODERATE | c.779A>G | p.Asn260Ser | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/12 | 910/2213 | 779/1257 | 260/418 | chr7 | 152823436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:152800631 | C | T | 1 | a0001c0007 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.201C>T | p.Ile67Ile | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/12 | 332/2213 | 201/1257 | 67/418 | chr7 | 152800631 | |||
chr7:152801683 | G | A | 1 | a0001c0003 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.288G>A | p.Val96Val | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/12 | 419/2213 | 288/1257 | 96/418 | chr7 | 152801683 | |||
chr7:152823386 | C | T | 1 | a0001c0002 | 2 | HG01884.hp1 HG02572.hp1 |
synonymous_variant | LOW | c.729C>T | p.Ala243Ala | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/12 | 860/2213 | 729/1257 | 243/418 | chr7 | 152823386 | |||
chr7:152825098 | C | T | 1 | a0001c0005 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.927C>T | p.Ile309Ile | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/12 | 1058/2213 | 927/1257 | 309/418 | chr7 | 152825098 | |||
chr7:152852210 | A | C | 1 | a0001c0004 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1036A>C | p.Arg346Arg | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/12 | 1167/2213 | 1036/1257 | 346/418 | chr7 | 152852210 | |||
chr7:152852239 | C | T | 1 | a0001c0004 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1065C>T | p.Gly355Gly | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/12 | 1196/2213 | 1065/1257 | 355/418 | chr7 | 152852239 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:152759774 | C | T | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0003t0003 |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | chr7 | 152759774 | |||||||
chr7:152759809 | T | C | 1 | a0001c0001t0008 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | 74 | chr7 | 152759809 | ||||||
chr7:152759824 | C | T | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(3): Show |
124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
5_prime_UTR_variant | MODIFIER | c.-59C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/12 | 59 | chr7 | 152759824 | ||||||
chr7:152854681 | G | A | 1 | a0001c0001t0009 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 128 | chr7 | 152854681 | ||||||
chr7:152854703 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | HG01099.hp1 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*150C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 150 | chr7 | 152854703 | ||||||
chr7:152854741 | G | C | 2 | a0001c0001t0005 a0001c0001t0008 |
3 | HG02723.hp2 HG02965.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*188G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 188 | chr7 | 152854741 | ||||||
chr7:152854781 | C | T | 1 | a0001c0001t0006 | 2 | NA18948.hp2 NA19002.hp2 |
3_prime_UTR_variant | MODIFIER | c.*228C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 228 | chr7 | 152854781 | ||||||
chr7:152854872 | A | T | 1 | a0001c0001t0007 | 2 | NA19010.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*319A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 319 | chr7 | 152854872 | ||||||
chr7:152854886 | C | T | 1 | a0001c0001t0004 | 3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 12/12 | 333 | chr7 | 152854886 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:152759968 | C | G | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+42C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152759968 | |||||||
chr7:152759971 | T | C | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | NA18939.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.44+45T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152759971 | |||||||
chr7:152760070 | G | T | 1 | a0001c0001t0001g0304 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.44+144G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760070 | |||||||
chr7:152760104 | C | A | 1 | a0001c0001t0002g0008 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.44+178C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760104 | |||||||
chr7:152760117 | G | C | 1 | a0001c0001t0002g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.44+191G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760117 | |||||||
chr7:152760173 | G | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | NA18988.hp2 NA19054.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.44+247G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760173 | |||||||
chr7:152760347 | C | T | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+421C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760347 | |||||||
chr7:152760457 | C | CACCT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+534_44+537dupCT others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152760457 | ||||||
chr7:152760457 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.44+531C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760457 | |||||||
chr7:152760598 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.44+672A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760598 | |||||||
chr7:152760630 | A | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+704A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760630 | |||||||
chr7:152760718 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0183 others(114): Show |
119 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.44+792C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760718 | |||||||
chr7:152760833 | G | A | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+907G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152760833 | |||||||
chr7:152761060 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.44+1134A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761060 | |||||||
chr7:152761096 | G | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.44+1170G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761096 | |||||||
chr7:152761304 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1378C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761304 | |||||||
chr7:152761368 | T | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG01361.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.44+1442T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761368 | |||||||
chr7:152761652 | CTTAGAAA others(3): Show |
C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1728_44+1737del others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152761652 | ||||||
chr7:152761661 | G | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.44+1735G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761661 | |||||||
chr7:152761663 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+1737T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761663 | |||||||
chr7:152761698 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+1772G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761698 | |||||||
chr7:152761730 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+1804A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761730 | |||||||
chr7:152761768 | C | T | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+1842C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761768 | |||||||
chr7:152761961 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.44+2035G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152761961 | |||||||
chr7:152762062 | C | T | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+2136C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762062 | |||||||
chr7:152762111 | T | G | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.44+2185T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762111 | |||||||
chr7:152762345 | T | C | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.44+2419T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762345 | |||||||
chr7:152762355 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+2429C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762355 | |||||||
chr7:152762570 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+2644A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762570 | |||||||
chr7:152762599 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.44+2673A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762599 | |||||||
chr7:152762602 | C | A | 96 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0007 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.44+2676C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762602 | |||||||
chr7:152762928 | C | T | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0108 others(1): Show |
4 | HG02055.hp1 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3002C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762928 | |||||||
chr7:152762956 | A | G | 7 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+3030A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152762956 | |||||||
chr7:152763313 | C | CA | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(80): Show |
85 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.44+3417dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | ||||||
chr7:152763313 | CA | C | 74 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(71): Show |
75 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.44+3417delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | ||||||
chr7:152763313 | CAA | C | 13 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(10): Show |
14 | HG01070.hp2 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3416_44+3417del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | ||||||
chr7:152763313 | CAAA | C | 13 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0276 others(10): Show |
13 | HG01109.hp1 HG01952.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.44+3415_44+3417del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152763313 | ||||||
chr7:152763502 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+3576C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763502 | |||||||
chr7:152763703 | C | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+3777C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763703 | |||||||
chr7:152763844 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.44+3918A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763844 | |||||||
chr7:152763978 | T | G | 1 | a0001c0001t0005g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.44+4052T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152763978 | |||||||
chr7:152764162 | C | G | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.44+4236C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764162 | |||||||
chr7:152764163 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(89): Show |
94 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.44+4237G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764163 | |||||||
chr7:152764319 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44+4393T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764319 | |||||||
chr7:152764435 | C | T | 8 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+4509C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764435 | |||||||
chr7:152764562 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+4636C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764562 | |||||||
chr7:152764630 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.44+4704C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764630 | |||||||
chr7:152764643 | CA | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(166): Show |
172 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.44+4732delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152764643 | ||||||
chr7:152764666 | T | G | 1 | a0001c0001t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44+4740T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764666 | |||||||
chr7:152764790 | C | CA | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+4865dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152764790 | ||||||
chr7:152764806 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44+4880C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764806 | |||||||
chr7:152764849 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+4923A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764849 | |||||||
chr7:152764858 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+4932A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152764858 | |||||||
chr7:152765109 | CT | C | 120 | a0001c0001t0001g0141 a0001c0001t0001g0183 a0001c0001t0001g0294 others(117): Show |
122 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.44+5205delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765109 | ||||||
chr7:152765127 | T | TTTC | 15 | a0001c0001t0001g0184 a0001c0001t0001g0220 a0001c0001t0001g0221 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+5203_44+5204ins others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765127 | ||||||
chr7:152765127 | T | TTTTC | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0185 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.44+5204_44+5205ins others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765127 | ||||||
chr7:152765132 | C | CTTTTT | 3 | a0001c0001t0001g0219 a0001c0001t0001g0248 a0001c0001t0001g0290 |
3 | HG01243.hp2 HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.44+5206_44+5207ins others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765132 | |||||||
chr7:152765132 | C | T | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(107): Show |
112 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.44+5206C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765132 | |||||||
chr7:152765252 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44+5326G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765252 | |||||||
chr7:152765298 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.44+5372A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765298 | |||||||
chr7:152765360 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.44+5434G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765360 | |||||||
chr7:152765415 | C | CT | 8 | a0001c0001t0001g0139 a0001c0001t0001g0181 a0001c0001t0001g0182 others(5): Show |
8 | HG00735.hp1 HG02135.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.44+5506dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152765415 | ||||||
chr7:152765593 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.44+5667T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765593 | |||||||
chr7:152765970 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+6044A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152765970 | |||||||
chr7:152766326 | A | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(117): Show |
122 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+6400A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766326 | |||||||
chr7:152766386 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6460C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766386 | |||||||
chr7:152766477 | G | A | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6551G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766477 | |||||||
chr7:152766617 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.44+6691T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766617 | |||||||
chr7:152766686 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+6760A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766686 | |||||||
chr7:152766803 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.44+6877T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766803 | |||||||
chr7:152766890 | G | A | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+6964G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152766890 | |||||||
chr7:152767013 | C | G | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7087C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767013 | |||||||
chr7:152767093 | G | GT | 31 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(28): Show |
31 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.44+7183dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | ||||||
chr7:152767093 | GT | G | 127 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(124): Show |
128 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.44+7183delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | ||||||
chr7:152767093 | GTT | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(113): Show |
118 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.44+7182_44+7183del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152767093 | ||||||
chr7:152767235 | C | G | 1 | a0001c0001t0002g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44+7309C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767235 | |||||||
chr7:152767306 | A | G | 73 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0008 others(70): Show |
73 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.44+7380A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767306 | |||||||
chr7:152767348 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7422A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767348 | |||||||
chr7:152767390 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44+7464G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767390 | |||||||
chr7:152767434 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44+7508C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767434 | |||||||
chr7:152767464 | T | C | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+7538T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767464 | |||||||
chr7:152767529 | A | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.44+7603A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767529 | |||||||
chr7:152767575 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+7649T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767575 | |||||||
chr7:152767591 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG01361.hp1 HG01496.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+7665A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767591 | |||||||
chr7:152767679 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.44+7753G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767679 | |||||||
chr7:152767835 | A | G | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+7909A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767835 | |||||||
chr7:152767853 | G | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+7927G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767853 | |||||||
chr7:152767875 | T | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(117): Show |
122 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+7949T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767875 | |||||||
chr7:152767980 | C | T | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+8054C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152767980 | |||||||
chr7:152768173 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8247A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768173 | |||||||
chr7:152768203 | A | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+8277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768203 | |||||||
chr7:152768241 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8315C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768241 | |||||||
chr7:152768419 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+8493T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768419 | |||||||
chr7:152768468 | C | T | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.44+8542C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768468 | |||||||
chr7:152768633 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+8707C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768633 | |||||||
chr7:152768664 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.44+8738C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768664 | |||||||
chr7:152768696 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+8770G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768696 | |||||||
chr7:152768733 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.44+8807C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768733 | |||||||
chr7:152768766 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+8840G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768766 | |||||||
chr7:152768766 | G | T | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.44+8840G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768766 | |||||||
chr7:152768775 | T | G | 9 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0157 others(6): Show |
10 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+8849T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768775 | |||||||
chr7:152768787 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0120 others(3): Show |
6 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+8861T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768787 | |||||||
chr7:152768889 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44+8963T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768889 | |||||||
chr7:152768893 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.44+8967G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152768893 | |||||||
chr7:152769000 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.44+9074C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769000 | |||||||
chr7:152769066 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.44+9140T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769066 | |||||||
chr7:152769161 | T | TTG | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+9247_44+9248dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769161 | ||||||
chr7:152769207 | T | A | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.44+9281T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769207 | |||||||
chr7:152769213 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+9287C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769213 | |||||||
chr7:152769289 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44+9363A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769289 | |||||||
chr7:152769298 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.44+9372C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769298 | |||||||
chr7:152769431 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.44+9505T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769431 | |||||||
chr7:152769574 | G | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.44+9648G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769574 | |||||||
chr7:152769782 | T | C | 25 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(22): Show |
25 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+9856T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152769782 | |||||||
chr7:152769869 | T | TA | 15 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0002g0009 others(12): Show |
15 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.44+9958dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769869 | ||||||
chr7:152769869 | TA | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(109): Show |
114 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.44+9958delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152769869 | ||||||
chr7:152770295 | G | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.44+10369G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770295 | |||||||
chr7:152770357 | T | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.44+10431T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770357 | |||||||
chr7:152770445 | C | G | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+10519C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770445 | |||||||
chr7:152770468 | G | A | 96 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0007 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.44+10542G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770468 | |||||||
chr7:152770683 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0161 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.44+10757T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770683 | |||||||
chr7:152770712 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.44+10786A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770712 | |||||||
chr7:152770720 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.44+10794T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770720 | |||||||
chr7:152770726 | AC | A | 8 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+10802delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152770726 | ||||||
chr7:152770784 | A | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+10858A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770784 | |||||||
chr7:152770786 | C | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+10860C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770786 | |||||||
chr7:152770807 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+10881G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770807 | |||||||
chr7:152770872 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+10946T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770872 | |||||||
chr7:152770995 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+11069G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152770995 | |||||||
chr7:152771062 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+11136T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771062 | |||||||
chr7:152771062 | T | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.44+11136T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771062 | |||||||
chr7:152771131 | T | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11205T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771131 | |||||||
chr7:152771297 | A | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.44+11371A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771297 | |||||||
chr7:152771373 | A | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11447A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771373 | |||||||
chr7:152771428 | T | G | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.44+11502T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771428 | |||||||
chr7:152771507 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44+11581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771507 | |||||||
chr7:152771541 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.44+11615G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771541 | |||||||
chr7:152771636 | T | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11551T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771636 | |||||||
chr7:152771655 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-11532A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771655 | |||||||
chr7:152771761 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11426G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771761 | |||||||
chr7:152771804 | G | A | 6 | a0001c0001t0001g0223 a0001c0001t0001g0247 a0001c0001t0002g0028 others(3): Show |
6 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-11383G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771804 | |||||||
chr7:152771851 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-11336A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771851 | |||||||
chr7:152771863 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0010 a0001c0001t0002g0011 others(3): Show |
6 | NA18949.hp2 NA18951.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-11324G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771863 | |||||||
chr7:152771919 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.45-11268G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152771919 | |||||||
chr7:152772133 | C | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(117): Show |
122 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.45-11054C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772133 | |||||||
chr7:152772146 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45-11041A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772146 | |||||||
chr7:152772307 | C | T | 1 | a0001c0001t0002g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.45-10880C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772307 | |||||||
chr7:152772313 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.45-10874G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772313 | |||||||
chr7:152772321 | A | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(117): Show |
122 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.45-10866A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772321 | |||||||
chr7:152772333 | ACATAG | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-10851_45-10847d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772333 | ||||||
chr7:152772351 | T | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-10836T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772351 | |||||||
chr7:152772396 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-10791G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772396 | |||||||
chr7:152772437 | A | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-10750A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772437 | |||||||
chr7:152772456 | T | TCAAGGTT others(4): Show |
1 | a0001c0001t0002g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.45-10730_45-10720d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772456 | ||||||
chr7:152772526 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-10661A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772526 | |||||||
chr7:152772532 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0286 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-10655A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772532 | |||||||
chr7:152772636 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.45-10551C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772636 | |||||||
chr7:152772695 | C | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.45-10492C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772695 | |||||||
chr7:152772770 | A | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-10417A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152772770 | |||||||
chr7:152772963 | ATATG | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.45-10221_45-10218d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772963 | ||||||
chr7:152772988 | A | AT | 94 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0007 others(91): Show |
94 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.45-10192dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152772988 | ||||||
chr7:152773144 | A | G | 1 | a0001c0001t0004g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45-10043A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773144 | |||||||
chr7:152773152 | CAA | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.45-10034_45-10033d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773152 | |||||||
chr7:152773314 | G | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-9873G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773314 | |||||||
chr7:152773403 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.45-9784A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773403 | |||||||
chr7:152773485 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-9702G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152773485 | |||||||
chr7:152774045 | C | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0161 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.45-9142C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774045 | |||||||
chr7:152774174 | T | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-9013T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774174 | |||||||
chr7:152774203 | C | T | 96 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0007 others(93): Show |
96 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.45-8984C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774203 | |||||||
chr7:152774223 | G | A | 8 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0066 others(5): Show |
8 | HG01257.hp2 NA18939.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-8964G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774223 | |||||||
chr7:152774244 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-8943C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774244 | |||||||
chr7:152774285 | C | T | 1 | a0001c0001t0002g0008 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.45-8902C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774285 | |||||||
chr7:152774292 | G | A | 23 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.45-8895G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774292 | |||||||
chr7:152774315 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0083 |
2 | NA18950.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.45-8872T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774315 | |||||||
chr7:152774382 | T | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-8805T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774382 | |||||||
chr7:152774405 | G | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-8782G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774405 | |||||||
chr7:152774439 | AT | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(92): Show |
97 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.45-8736delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152774439 | ||||||
chr7:152774716 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45-8471A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774716 | |||||||
chr7:152774721 | A | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-8466A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774721 | |||||||
chr7:152774752 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.45-8435C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774752 | |||||||
chr7:152774775 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.45-8412C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774775 | |||||||
chr7:152774849 | A | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-8338A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774849 | |||||||
chr7:152774862 | G | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-8325G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774862 | |||||||
chr7:152774863 | C | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-8324C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774863 | |||||||
chr7:152774946 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.45-8241G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774946 | |||||||
chr7:152774960 | A | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(124): Show |
129 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.45-8227A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152774960 | |||||||
chr7:152775060 | C | T | 6 | a0001c0001t0001g0294 a0001c0001t0001g0297 a0001c0001t0001g0302 others(3): Show |
7 | HG01884.hp2 HG01952.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-8127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775060 | |||||||
chr7:152775190 | C | CA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(31): Show |
36 | HG00642.hp2 HG01099.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.45-7971dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | ||||||
chr7:152775190 | C | CAA | 11 | a0001c0001t0001g0113 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
11 | HG01496.hp1 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-7972_45-7971dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | ||||||
chr7:152775190 | CA | C | 77 | a0001c0001t0001g0017 a0001c0001t0001g0183 a0001c0001t0001g0212 others(74): Show |
77 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.45-7971delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | ||||||
chr7:152775190 | CAA | C | 10 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0297 others(7): Show |
10 | HG01070.hp2 HG01952.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-7972_45-7971del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775190 | ||||||
chr7:152775215 | AAG | A | 7 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(4): Show |
7 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-7970_45-7969del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775215 | ||||||
chr7:152775216 | AG | A | 3 | a0001c0001t0003g0268 a0001c0001t0004g0171 a0001c0001t0004g0172 |
3 | HG02976.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.45-7970delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775216 | |||||||
chr7:152775217 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.45-7970G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775217 | |||||||
chr7:152775448 | C | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02074.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.45-7739C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775448 | |||||||
chr7:152775743 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.45-7444G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775743 | |||||||
chr7:152775759 | C | CA | 27 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0269 others(24): Show |
27 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.45-7414dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152775759 | ||||||
chr7:152775774 | T | C | 5 | a0001c0001t0001g0186 a0001c0001t0001g0191 a0001c0001t0001g0226 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-7413T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775774 | |||||||
chr7:152775839 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0120 others(3): Show |
6 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-7348A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775839 | |||||||
chr7:152775841 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0167 |
2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.45-7346G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152775841 | |||||||
chr7:152776137 | A | G | 2 | a0001c0001t0003g0174 a0001c0001t0003g0175 |
2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.45-7050A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776137 | |||||||
chr7:152776219 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6968T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776219 | |||||||
chr7:152776247 | G | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6940G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776247 | |||||||
chr7:152776532 | C | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0300 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.45-6655C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776532 | |||||||
chr7:152776576 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.45-6611A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776576 | |||||||
chr7:152776677 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6510A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776677 | |||||||
chr7:152776882 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.45-6305A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776882 | |||||||
chr7:152776954 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-6233A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776954 | |||||||
chr7:152776956 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-6231A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776956 | |||||||
chr7:152776969 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.45-6218C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776969 | |||||||
chr7:152776970 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45-6217G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152776970 | |||||||
chr7:152777015 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.45-6172C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777015 | |||||||
chr7:152777016 | G | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-6171G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777016 | |||||||
chr7:152777026 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.45-6161G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777026 | |||||||
chr7:152777388 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-5799T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777388 | |||||||
chr7:152777438 | C | T | 1 | a0002c0006t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.45-5749C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777438 | |||||||
chr7:152777525 | GTTC | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-5659_45-5657del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152777525 | ||||||
chr7:152777564 | A | G | 1 | a0001c0001t0002g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.45-5623A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777564 | |||||||
chr7:152777624 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(114): Show |
119 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.45-5563C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777624 | |||||||
chr7:152777644 | T | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-5543T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777644 | |||||||
chr7:152777750 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45-5437A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777750 | |||||||
chr7:152777865 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-5322G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152777865 | |||||||
chr7:152777940 | A | AC | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.45-5246dupC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152777940 | ||||||
chr7:152778156 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
300 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(297): Show |
intron_variant | MODIFIER | c.45-5031T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778156 | |||||||
chr7:152778227 | A | AT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG00735.hp2 HG01099.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-4943dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | ||||||
chr7:152778227 | AT | A | 19 | a0001c0001t0001g0154 a0001c0001t0001g0247 a0001c0001t0001g0269 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4943delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | ||||||
chr7:152778227 | ATT | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(96): Show |
101 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.45-4944_45-4943del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778227 | ||||||
chr7:152778261 | T | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4926T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778261 | |||||||
chr7:152778377 | G | A | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.45-4810G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778377 | |||||||
chr7:152778443 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-4744G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778443 | |||||||
chr7:152778668 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-4519G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778668 | |||||||
chr7:152778791 | A | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0157 others(6): Show |
10 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-4396A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778791 | |||||||
chr7:152778891 | C | T | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-4296C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778891 | |||||||
chr7:152778911 | C | G | 1 | a0001c0001t0002g0008 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.45-4276C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778911 | |||||||
chr7:152778943 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0150 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.45-4211_45-4202dup others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0002g0009 a0001c0001t0002g0157 |
2 | HG02896.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.45-4212_45-4202dup others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0124 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.45-4218_45-4202dup others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CA | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0122 others(6): Show |
9 | HG01081.hp2 HG02809.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-4202delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAA | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0123 a0001c0001t0001g0125 others(5): Show |
8 | HG00597.hp1 HG01496.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-4203_45-4202del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAA | C | 13 | a0001c0001t0001g0115 a0001c0001t0001g0131 a0001c0001t0001g0132 others(10): Show |
13 | HG00544.hp2 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-4204_45-4202del others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAA | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0113 a0001c0001t0001g0117 others(8): Show |
12 | HG01099.hp1 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-4205_45-4202del others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0002g0023 a0001c0001t0002g0030 a0001c0001t0002g0088 |
3 | HG01346.hp1 HG02132.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.45-4212_45-4202del others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(5): Show |
C | 34 | a0001c0001t0001g0182 a0001c0001t0002g0012 a0001c0001t0002g0019 others(31): Show |
34 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.45-4213_45-4202del others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(6): Show |
C | 51 | a0001c0001t0001g0183 a0001c0001t0002g0006 a0001c0001t0002g0007 others(48): Show |
51 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.45-4214_45-4202del others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0109 others(4): Show |
7 | HG01361.hp2 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-4215_45-4202del others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(8): Show |
C | 11 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0179 others(8): Show |
12 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-4216_45-4202del others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(9): Show |
C | 22 | a0001c0001t0001g0112 a0001c0001t0001g0188 a0001c0001t0001g0189 others(19): Show |
22 | HG00099.hp1 HG00423.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.45-4217_45-4202del others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(10): Show |
C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0185 others(63): Show |
68 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.45-4218_45-4202del others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(11): Show |
C | 26 | a0001c0001t0001g0184 a0001c0001t0001g0219 a0001c0001t0001g0223 others(23): Show |
26 | HG01109.hp1 HG01256.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.45-4219_45-4202del others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(12): Show |
C | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0250 others(1): Show |
4 | HG00735.hp1 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4220_45-4202del others(19): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(15): Show |
C | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-4223_45-4202del others(22): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45-4224_45-4202del others(23): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(19): Show |
C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-4227_45-4202del others(26): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778943 | CAAAAAAA others(23): Show |
C | 7 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(4): Show |
7 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-4231_45-4202del others(30): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152778943 | ||||||
chr7:152778985 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.45-4202A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152778985 | |||||||
chr7:152779014 | C | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0184 a0001c0001t0001g0185 others(76): Show |
80 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.45-4173C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779014 | |||||||
chr7:152779038 | T | G | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.45-4149T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779038 | |||||||
chr7:152779044 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(117): Show |
122 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.45-4143C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779044 | |||||||
chr7:152779203 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-3984G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779203 | |||||||
chr7:152779257 | C | T | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-3930C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779257 | |||||||
chr7:152779259 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.45-3928C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779259 | |||||||
chr7:152779263 | C | T | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-3924C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779263 | |||||||
chr7:152779264 | A | G | 9 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(6): Show |
9 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-3923A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779264 | |||||||
chr7:152779456 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.45-3731C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779456 | |||||||
chr7:152779496 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45-3691C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779496 | |||||||
chr7:152779700 | A | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-3487A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779700 | |||||||
chr7:152779732 | G | C | 1 | a0001c0001t0005g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.45-3455G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779732 | |||||||
chr7:152779996 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-3191T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152779996 | |||||||
chr7:152780011 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.45-3176C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780011 | |||||||
chr7:152780118 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0177 others(1): Show |
4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3069T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780118 | |||||||
chr7:152780158 | T | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0177 others(1): Show |
4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3029T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780158 | |||||||
chr7:152780166 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-3021C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780166 | |||||||
chr7:152780190 | C | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0069 |
2 | HG01361.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.45-2997C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780190 | |||||||
chr7:152780208 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.45-2979G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780208 | |||||||
chr7:152780208 | G | C | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.45-2979G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780208 | |||||||
chr7:152780266 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-2921G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780266 | |||||||
chr7:152780283 | G | A | 220 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(217): Show |
222 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.45-2904G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780283 | |||||||
chr7:152780329 | C | G | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.45-2858C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780329 | |||||||
chr7:152780339 | C | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.45-2848C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780339 | |||||||
chr7:152780352 | C | CAA | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(212): Show |
217 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.45-2822_45-2821dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780352 | ||||||
chr7:152780395 | G | A | 218 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(215): Show |
220 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.45-2792G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780395 | |||||||
chr7:152780456 | C | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-2731C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780456 | |||||||
chr7:152780487 | A | T | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.45-2700A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780487 | |||||||
chr7:152780530 | T | C | 7 | a0001c0001t0001g0273 a0001c0001t0001g0300 a0001c0001t0002g0028 others(4): Show |
7 | HG02280.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-2657T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780530 | |||||||
chr7:152780539 | G | A | 2 | a0001c0001t0001g0273 a0001c0001t0008g0305 |
2 | HG02965.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.45-2648G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780539 | |||||||
chr7:152780569 | T | C | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.45-2618T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780569 | |||||||
chr7:152780844 | A | AT | 9 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0002g0046 others(6): Show |
9 | HG00438.hp2 HG00735.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-2325dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | ||||||
chr7:152780844 | A | ATT | 9 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0300 others(6): Show |
10 | HG01952.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.45-2326_45-2325dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | ||||||
chr7:152780844 | AT | A | 27 | a0001c0001t0001g0149 a0001c0001t0001g0269 a0001c0001t0001g0270 others(24): Show |
28 | HG01109.hp1 HG01192.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.45-2325delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | ||||||
chr7:152780844 | ATT | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.45-2326_45-2325del others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152780844 | ||||||
chr7:152780888 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-2299C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780888 | |||||||
chr7:152780914 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-2273T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780914 | |||||||
chr7:152780948 | G | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-2239G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152780948 | |||||||
chr7:152781100 | G | T | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(128): Show |
134 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.45-2087G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781100 | |||||||
chr7:152781143 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-2044T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781143 | |||||||
chr7:152781169 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.45-2018C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781169 | |||||||
chr7:152781178 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.45-2009A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781178 | |||||||
chr7:152781193 | G | GT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0113 a0001c0001t0001g0124 others(97): Show |
101 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.45-1971dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | ||||||
chr7:152781193 | G | GTT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
17 | HG00423.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-1972_45-1971dup others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | ||||||
chr7:152781193 | GT | G | 9 | a0001c0001t0001g0110 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG01070.hp2 HG01081.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-1971delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152781193 | ||||||
chr7:152781198 | T | G | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45-1989T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781198 | |||||||
chr7:152781299 | T | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(91): Show |
96 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.45-1888T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781299 | |||||||
chr7:152781356 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-1831G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781356 | |||||||
chr7:152781369 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.45-1818C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781369 | |||||||
chr7:152781375 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.45-1812T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781375 | |||||||
chr7:152781477 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.45-1710G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781477 | |||||||
chr7:152781767 | C | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.45-1420C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781767 | |||||||
chr7:152781818 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.45-1369C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781818 | |||||||
chr7:152781911 | C | T | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-1276C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152781911 | |||||||
chr7:152782033 | G | GT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0286 others(9): Show |
13 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-1145dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152782033 | ||||||
chr7:152782118 | ATCGTAAA others(10): Show |
A | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.45-1067_45-1051del others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152782118 | ||||||
chr7:152782231 | G | A | 131 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(128): Show |
134 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.45-956G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782231 | |||||||
chr7:152782289 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0184 others(110): Show |
115 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.45-898G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782289 | |||||||
chr7:152782705 | T | C | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-482T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782705 | |||||||
chr7:152782856 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.45-331C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152782856 | |||||||
chr7:152783015 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-172A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783015 | |||||||
chr7:152783043 | G | GT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0114 others(90): Show |
95 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.45-125dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | ||||||
chr7:152783043 | G | GTT | 12 | a0001c0001t0001g0197 a0001c0001t0002g0023 a0001c0001t0002g0046 others(9): Show |
12 | HG00438.hp1 HG01255.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-126_45-125dupTT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | ||||||
chr7:152783043 | GT | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0131 others(89): Show |
94 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.45-125delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | ||||||
chr7:152783043 | GTT | G | 13 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG01099.hp2 HG01106.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.45-126_45-125delTT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152783043 | ||||||
chr7:152783045 | T | G | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0302 others(1): Show |
4 | HG01952.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-142T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783045 | |||||||
chr7:152783046 | T | G | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-141T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783046 | |||||||
chr7:152783049 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-138T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783049 | |||||||
chr7:152783141 | G | A | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.45-46G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 1/11 | chr7 | 152783141 | |||||||
chr7:152783361 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+119G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783361 | |||||||
chr7:152783426 | G | A | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+184G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783426 | |||||||
chr7:152783465 | T | TGGGTCCC others(10): Show |
1 | a0001c0001t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+223_100+224ins others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783465 | |||||||
chr7:152783479 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+237C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783479 | |||||||
chr7:152783489 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+247C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783489 | |||||||
chr7:152783603 | C | T | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
39 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+361C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783603 | |||||||
chr7:152783612 | CT | C | 8 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0059 others(5): Show |
9 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+381delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152783612 | ||||||
chr7:152783733 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+491G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783733 | |||||||
chr7:152783775 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+533G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783775 | |||||||
chr7:152783888 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100+646G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783888 | |||||||
chr7:152783926 | T | C | 1 | a0001c0003t0003g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.100+684T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783926 | |||||||
chr7:152783957 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+715G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783957 | |||||||
chr7:152783958 | C | G | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+716C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152783958 | |||||||
chr7:152784017 | G | A | 23 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.100+775G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784017 | |||||||
chr7:152784045 | G | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+803G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784045 | |||||||
chr7:152784090 | CA | C | 6 | a0001c0001t0001g0154 a0001c0001t0001g0195 a0001c0001t0002g0011 others(3): Show |
6 | HG01257.hp2 HG02965.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+861delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152784090 | ||||||
chr7:152784281 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100+1039G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784281 | |||||||
chr7:152784298 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.100+1056G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784298 | |||||||
chr7:152784303 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0228 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.100+1061G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784303 | |||||||
chr7:152784491 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.100+1249T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784491 | |||||||
chr7:152784577 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1335T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784577 | |||||||
chr7:152784657 | C | G | 1 | a0001c0001t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1415C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784657 | |||||||
chr7:152784694 | G | C | 1 | a0001c0001t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1452G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784694 | |||||||
chr7:152784707 | T | C | 1 | a0001c0001t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100+1465T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784707 | |||||||
chr7:152784774 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+1532G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784774 | |||||||
chr7:152784844 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+1602C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784844 | |||||||
chr7:152784867 | C | T | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+1625C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784867 | |||||||
chr7:152784948 | C | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(15): Show |
19 | HG00738.hp1 HG01071.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+1706C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152784948 | |||||||
chr7:152785017 | C | T | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+1775C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785017 | |||||||
chr7:152785026 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+1784C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785026 | |||||||
chr7:152785086 | CTTG | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+1847_100+1849d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785086 | ||||||
chr7:152785146 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+1904A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785146 | |||||||
chr7:152785271 | G | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+2029G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785271 | |||||||
chr7:152785374 | TGTGAGGG others(103): Show |
T | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100+2134_100+2243d others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785374 | ||||||
chr7:152785374 | TGTGAGGG others(105): Show |
T | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+2134_100+2245d others(2): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785374 | ||||||
chr7:152785376 | T | TG | 39 | a0001c0001t0001g0214 a0001c0001t0001g0222 a0001c0001t0001g0245 others(36): Show |
39 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+2135dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | ||||||
chr7:152785376 | T | TGA | 6 | a0001c0001t0001g0183 a0001c0001t0002g0062 a0001c0001t0002g0068 others(3): Show |
6 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2136_100+2137d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | ||||||
chr7:152785376 | T | TGAGAGA | 10 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(7): Show |
10 | HG01934.hp2 HG01952.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | ||||||
chr7:152785376 | T | TGG | 10 | a0001c0001t0001g0196 a0001c0001t0001g0236 a0001c0001t0002g0020 others(7): Show |
10 | HG00735.hp2 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+2135_100+2136i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785376 | ||||||
chr7:152785377 | GA | G | 13 | a0001c0001t0001g0197 a0001c0001t0001g0211 a0001c0001t0001g0238 others(10): Show |
13 | HG00738.hp1 HG02083.hp2 HG03239.hp2 others(10): Show |
intron_variant | MODIFIER | c.100+2136delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785377 | |||||||
chr7:152785378 | A | AG | 21 | a0001c0001t0001g0024 a0001c0001t0001g0112 a0001c0001t0001g0113 others(18): Show |
21 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+2146dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785378 | ||||||
chr7:152785378 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0209 others(99): Show |
103 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.100+2136A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785378 | |||||||
chr7:152785379 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.100+2137G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | |||||||
chr7:152785379 | G | GA | 12 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0028 others(9): Show |
12 | HG02055.hp1 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | |||||||
chr7:152785379 | G | GAGAGA | 43 | a0001c0001t0001g0005 a0001c0001t0001g0190 a0001c0001t0001g0198 others(40): Show |
45 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.100+2137_100+2138i others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785379 | |||||||
chr7:152785380 | G | A | 49 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0184 others(46): Show |
49 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.100+2138G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785380 | |||||||
chr7:152785381 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0190 a0001c0001t0001g0198 others(36): Show |
41 | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.100+2139G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785381 | |||||||
chr7:152785382 | G | A | 42 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2140G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785382 | |||||||
chr7:152785383 | G | C | 1 | a0001c0001t0002g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100+2141G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785383 | |||||||
chr7:152785384 | G | A | 42 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785384 | |||||||
chr7:152785386 | G | A | 42 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2144G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785386 | |||||||
chr7:152785389 | A | AGGGGAGG others(37): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+2164_100+2207d others(46): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785389 | ||||||
chr7:152785389 | A | G | 43 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(40): Show |
43 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.100+2147A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785389 | |||||||
chr7:152785394 | A | G | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2152A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785394 | |||||||
chr7:152785394 | AG | A | 41 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(38): Show |
41 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.100+2157delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785394 | ||||||
chr7:152785395 | G | A | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2153G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785395 | |||||||
chr7:152785402 | GGGGAGAG others(3): Show |
G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2178_100+2187d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785402 | ||||||
chr7:152785406 | AGAGG | A | 42 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2172_100+2175d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785406 | ||||||
chr7:152785412 | A | G | 42 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(39): Show |
42 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+2170A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785412 | |||||||
chr7:152785420 | GGAGGGAG others(3): Show |
G | 1 | a0001c0001t0001g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100+2184_100+2193d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785420 | ||||||
chr7:152785428 | A | AGAGAGGG others(14): Show |
1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.100+2196_100+2216d others(23): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785428 | ||||||
chr7:152785432 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2190A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785432 | |||||||
chr7:152785432 | AG | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+2195delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785432 | ||||||
chr7:152785438 | A | AGGGGGAG others(9): Show |
2 | a0001c0002t0001g0192 a0001c0002t0001g0194 |
2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.100+2208_100+2223d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785438 | ||||||
chr7:152785441 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2199G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785441 | |||||||
chr7:152785447 | G | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
5 | HG00741.hp1 HG01175.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2205G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785447 | |||||||
chr7:152785453 | A | AG | 15 | a0001c0001t0001g0004 a0001c0001t0001g0147 a0001c0001t0001g0185 others(12): Show |
15 | HG00609.hp1 HG01109.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+2217dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785453 | ||||||
chr7:152785470 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0002g0009 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+2228G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785470 | |||||||
chr7:152785470 | G | GGGAGAGG others(27): Show |
1 | a0001c0001t0002g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.100+2229_100+2230i others(36): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785470 | ||||||
chr7:152785474 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0002g0009 a0001c0001t0002g0039 |
3 | HG00544.hp1 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.100+2232G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785474 | |||||||
chr7:152785474 | G | GGGGAGAG others(5): Show |
2 | a0001c0001t0002g0057 a0001c0001t0008g0305 |
2 | HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100+2233_100+2234i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785474 | ||||||
chr7:152785479 | G | GAGAGAGA others(7): Show |
1 | a0001c0001t0001g0209 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100+2251_100+2264d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785479 | ||||||
chr7:152785481 | G | C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0057 a0001c0001t0008g0305 |
3 | HG00544.hp1 HG00735.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.100+2239G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785481 | |||||||
chr7:152785481 | G | GAGACAGA others(5): Show |
1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100+2242_100+2243i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | ||||||
chr7:152785481 | G | GAGAGAGA others(3): Show |
117 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
120 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.100+2248_100+2249i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | ||||||
chr7:152785481 | G | GAGAGAGA others(5): Show |
113 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(110): Show |
114 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.100+2251_100+2262d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | ||||||
chr7:152785481 | G | GAGAGAGA others(7): Show |
2 | a0001c0001t0002g0035 a0001c0001t0002g0045 |
2 | NA18949.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.100+2250_100+2251i others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785481 | ||||||
chr7:152785493 | C | G | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2251C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785493 | |||||||
chr7:152785504 | A | ACAGAGAG others(12): Show |
1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2262_100+2263i others(21): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785504 | |||||||
chr7:152785510 | AG | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2270delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785510 | ||||||
chr7:152785512 | G | A | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100+2270G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785512 | |||||||
chr7:152785512 | G | GAGAGAGA | 35 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
36 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+2278_100+2284d others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785512 | ||||||
chr7:152785518 | GA | G | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+2278delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152785518 | ||||||
chr7:152785542 | G | A | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0167 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+2300G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785542 | |||||||
chr7:152785640 | C | T | 69 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(66): Show |
70 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.100+2398C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785640 | |||||||
chr7:152785659 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+2417T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785659 | |||||||
chr7:152785721 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0077 |
3 | HG00423.hp1 HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.100+2479C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785721 | |||||||
chr7:152785722 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(9): Show |
12 | HG01099.hp2 HG02083.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2480G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785722 | |||||||
chr7:152785945 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0262 |
3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.100+2703G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152785945 | |||||||
chr7:152786058 | C | T | 136 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(133): Show |
138 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.100+2816C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786058 | |||||||
chr7:152786084 | G | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2842G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786084 | |||||||
chr7:152786173 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+2931G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786173 | |||||||
chr7:152786281 | G | A | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+3039G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786281 | |||||||
chr7:152786399 | A | G | 16 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0026 others(13): Show |
16 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+3157A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786399 | |||||||
chr7:152786410 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100+3168C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786410 | |||||||
chr7:152786482 | G | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+3240G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786482 | |||||||
chr7:152786548 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.100+3306G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786548 | |||||||
chr7:152786549 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+3307T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786549 | |||||||
chr7:152786552 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100+3310C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786552 | |||||||
chr7:152786552 | CG | C | 4 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(1): Show |
5 | HG02630.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+3311delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786552 | |||||||
chr7:152786553 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100+3311G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786553 | |||||||
chr7:152786553 | G | GA | 10 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG00438.hp2 HG01175.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+3326dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152786553 | ||||||
chr7:152786553 | GA | G | 38 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(35): Show |
39 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.100+3326delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152786553 | ||||||
chr7:152786659 | A | C | 214 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0183 others(211): Show |
217 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.100+3417A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786659 | |||||||
chr7:152786772 | A | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.100+3530A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786772 | |||||||
chr7:152786848 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+3606T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786848 | |||||||
chr7:152786955 | G | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0210 a0001c0001t0001g0224 others(2): Show |
5 | HG02630.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+3713G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152786955 | |||||||
chr7:152787226 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+3984T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787226 | |||||||
chr7:152787303 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100+4061A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787303 | |||||||
chr7:152787352 | T | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.100+4110T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787352 | |||||||
chr7:152787681 | C | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+4439C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787681 | |||||||
chr7:152787711 | C | T | 1 | a0001c0001t0002g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.100+4469C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787711 | |||||||
chr7:152787777 | A | G | 17 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0026 others(14): Show |
17 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+4535A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787777 | |||||||
chr7:152787811 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(90): Show |
94 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.100+4569C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787811 | |||||||
chr7:152787878 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+4636A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787878 | |||||||
chr7:152787887 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.100+4645T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152787887 | |||||||
chr7:152788025 | A | C | 1 | a0001c0001t0001g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.100+4783A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788025 | |||||||
chr7:152788049 | C | T | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+4807C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788049 | |||||||
chr7:152788079 | CACGTCCA others(25): Show |
C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.100+4871_100+4902d others(34): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788079 | ||||||
chr7:152788175 | TG | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.100+4936delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788175 | ||||||
chr7:152788251 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.100+5009C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788251 | |||||||
chr7:152788295 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.100+5053G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788295 | |||||||
chr7:152788299 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+5057A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788299 | |||||||
chr7:152788411 | G | GT | 83 | a0001c0001t0001g0005 a0001c0001t0001g0116 a0001c0001t0001g0125 others(80): Show |
84 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.100+5187dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788411 | ||||||
chr7:152788411 | GT | G | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5187delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152788411 | ||||||
chr7:152788466 | C | T | 1 | a0001c0001t0010g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.100+5224C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788466 | |||||||
chr7:152788497 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+5255C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788497 | |||||||
chr7:152788504 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5262C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788504 | |||||||
chr7:152788662 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+5420C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788662 | |||||||
chr7:152788769 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5527C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788769 | |||||||
chr7:152788813 | G | C | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+5571G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788813 | |||||||
chr7:152788832 | G | A | 23 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
23 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.100+5590G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788832 | |||||||
chr7:152788897 | C | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0235 |
3 | NA18951.hp1 NA19056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.100+5655C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788897 | |||||||
chr7:152788914 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0144 |
2 | HG00741.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.100+5672T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788914 | |||||||
chr7:152788999 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5757G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152788999 | |||||||
chr7:152789000 | C | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5758C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789000 | |||||||
chr7:152789014 | G | T | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0300 others(4): Show |
8 | HG02615.hp1 HG02630.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5772G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789014 | |||||||
chr7:152789023 | A | AAAC | 14 | a0001c0001t0001g0258 a0001c0001t0002g0008 a0001c0001t0002g0009 others(11): Show |
14 | HG00738.hp2 HG01074.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+5808_100+5810d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | ||||||
chr7:152789023 | A | AAACAAC | 104 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(101): Show |
105 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.100+5805_100+5810d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | ||||||
chr7:152789023 | A | AAACAACA others(5): Show |
1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100+5799_100+5810d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | ||||||
chr7:152789023 | AAAC | A | 10 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0113 others(7): Show |
10 | HG01081.hp2 HG01192.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+5808_100+5810d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | ||||||
chr7:152789023 | AAACAAC | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5805_100+5810d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789023 | ||||||
chr7:152789041 | C | CAATA | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5801_100+5802i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789041 | ||||||
chr7:152789043 | A | ATAAACAG | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+5801_100+5802i others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789043 | |||||||
chr7:152789043 | A | G | 1 | a0001c0001t0005g0261 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+5801A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789043 | |||||||
chr7:152789046 | A | ACAAACAG | 14 | a0001c0001t0001g0005 a0001c0001t0001g0220 a0001c0001t0001g0221 others(11): Show |
15 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+5807_100+5808i others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789046 | ||||||
chr7:152789046 | A | G | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5804A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789046 | |||||||
chr7:152789047 | C | CA | 39 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(36): Show |
39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.100+5807dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789047 | ||||||
chr7:152789049 | A | AACAG | 18 | a0001c0001t0001g0184 a0001c0001t0001g0190 a0001c0001t0001g0205 others(15): Show |
18 | HG00597.hp2 HG01884.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+5807_100+5808i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789049 | |||||||
chr7:152789050 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0246 |
2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5808C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789050 | |||||||
chr7:152789050 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5808C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789050 | |||||||
chr7:152789051 | A | AAC | 34 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0190 others(31): Show |
35 | HG00099.hp1 HG00597.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.100+5810_100+5811i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789051 | ||||||
chr7:152789051 | A | AGC | 39 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(36): Show |
39 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.100+5809_100+5810i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789051 | |||||||
chr7:152789051 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0246 |
2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5809A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789051 | |||||||
chr7:152789053 | A | C | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5811A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789053 | |||||||
chr7:152789053 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0246 |
2 | HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.100+5811A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789053 | |||||||
chr7:152789054 | C | A | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+5812C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789054 | |||||||
chr7:152789056 | G | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0181 a0001c0001t0001g0182 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.100+5814G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789056 | |||||||
chr7:152789063 | CA | C | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0277 others(5): Show |
8 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+5824delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789063 | ||||||
chr7:152789064 | A | AAAC | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5840_100+5842d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789064 | A | AAC | 91 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(88): Show |
92 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.100+5823_100+5824i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789064 | A | AACAACAA others(4): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.100+5823_100+5824i others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789064 | A | AACAACAA others(7): Show |
1 | a0001c0001t0001g0014 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.100+5823_100+5824i others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789064 | A | AACAACAA others(10): Show |
1 | a0001c0001t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100+5823_100+5824i others(19): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789064 | AAAC | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(110): Show |
114 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.100+5840_100+5842d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789064 | ||||||
chr7:152789066 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0002g0072 |
2 | HG00099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.100+5824A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789066 | |||||||
chr7:152789067 | C | A | 2 | a0001c0001t0001g0240 a0001c0001t0002g0072 |
2 | HG00099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.100+5825C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789067 | |||||||
chr7:152789074 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+5832A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789074 | |||||||
chr7:152789215 | A | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+5973A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789215 | |||||||
chr7:152789231 | A | C | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5989A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789231 | |||||||
chr7:152789261 | G | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
93 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.100+6019G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789261 | |||||||
chr7:152789284 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(3): Show |
7 | HG02257.hp1 HG02630.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+6042C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789284 | |||||||
chr7:152789348 | T | C | 104 | a0001c0001t0001g0005 a0001c0001t0001g0181 a0001c0001t0001g0182 others(101): Show |
106 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.100+6106T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789348 | |||||||
chr7:152789356 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100+6114C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789356 | |||||||
chr7:152789375 | C | T | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6133C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789375 | |||||||
chr7:152789466 | G | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0094 |
2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.100+6224G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789466 | |||||||
chr7:152789487 | T | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+6245T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789487 | |||||||
chr7:152789497 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100+6255A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789497 | |||||||
chr7:152789511 | A | T | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6269A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789511 | |||||||
chr7:152789519 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100+6277G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789519 | |||||||
chr7:152789549 | AT | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0220 a0001c0001t0001g0240 others(11): Show |
15 | HG00609.hp2 HG01109.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+6319delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789549 | ||||||
chr7:152789549 | ATTT | A | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6317_100+6319d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789549 | ||||||
chr7:152789566 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+6324C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789566 | |||||||
chr7:152789567 | A | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+6325A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789567 | |||||||
chr7:152789605 | G | C | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+6363G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789605 | |||||||
chr7:152789613 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.100+6371A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789613 | |||||||
chr7:152789735 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6493G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789735 | |||||||
chr7:152789745 | C | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+6503C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789745 | |||||||
chr7:152789904 | T | TA | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6669dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789904 | ||||||
chr7:152789914 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+6672A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789914 | |||||||
chr7:152789930 | A | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+6688A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152789930 | |||||||
chr7:152789997 | C | CT | 92 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0162 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.100+6777dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | ||||||
chr7:152789997 | C | CTTT | 17 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(14): Show |
17 | HG00735.hp1 HG01109.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+6775_100+6777d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | ||||||
chr7:152789997 | CT | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(16): Show |
20 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.100+6777delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152789997 | ||||||
chr7:152790044 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+6802G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790044 | |||||||
chr7:152790136 | A | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+6894A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790136 | |||||||
chr7:152790254 | A | G | 19 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0270 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+7012A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790254 | |||||||
chr7:152790312 | T | A | 1 | a0001c0001t0002g0020 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.100+7070T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790312 | |||||||
chr7:152790323 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0216 a0001c0001t0001g0217 others(12): Show |
16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+7081C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790323 | |||||||
chr7:152790373 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.100+7131G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790373 | |||||||
chr7:152790481 | A | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7239A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790481 | |||||||
chr7:152790489 | A | G | 1 | a0001c0001t0002g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100+7247A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790489 | |||||||
chr7:152790641 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.100+7399A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790641 | |||||||
chr7:152790869 | C | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+7627C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790869 | |||||||
chr7:152790941 | A | T | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7699A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790941 | |||||||
chr7:152790987 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100+7745G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152790987 | |||||||
chr7:152791015 | CT | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG01099.hp2 HG01106.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.100+7789delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152791015 | ||||||
chr7:152791156 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+7914G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791156 | |||||||
chr7:152791171 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100+7929C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791171 | |||||||
chr7:152791202 | G | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0198 a0001c0001t0001g0204 |
3 | NA18981.hp1 NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.100+7960G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791202 | |||||||
chr7:152791209 | T | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.100+7967T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152791209 | |||||||
chr7:152792035 | G | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-8496G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792035 | |||||||
chr7:152792138 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.101-8393C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792138 | |||||||
chr7:152792305 | A | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-8226A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792305 | |||||||
chr7:152792335 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0120 a0001c0001t0001g0121 others(1): Show |
4 | HG01361.hp1 HG01496.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-8196G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792335 | |||||||
chr7:152792450 | T | C | 36 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.101-8081T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792450 | |||||||
chr7:152792471 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG00735.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.101-8060C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792471 | |||||||
chr7:152792616 | G | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-7915G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792616 | |||||||
chr7:152792709 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-7822C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792709 | |||||||
chr7:152792710 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.101-7821T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792710 | |||||||
chr7:152792768 | A | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-7763A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792768 | |||||||
chr7:152792778 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-7753C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792778 | |||||||
chr7:152792869 | A | C | 1 | a0001c0001t0002g0006 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.101-7662A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792869 | |||||||
chr7:152792892 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.101-7639A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792892 | |||||||
chr7:152792940 | T | TAA | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(4): Show |
7 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-7591_101-7590i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792940 | |||||||
chr7:152792964 | C | CT | 25 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(22): Show |
25 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-7558dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152792964 | ||||||
chr7:152792981 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-7550A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152792981 | |||||||
chr7:152793022 | A | AT | 10 | a0001c0001t0001g0122 a0001c0001t0001g0244 a0001c0001t0001g0258 others(7): Show |
10 | HG00423.hp1 HG01081.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-7489dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793022 | ||||||
chr7:152793022 | AT | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.101-7489delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793022 | ||||||
chr7:152793084 | A | G | 1 | a0001c0001t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101-7447A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793084 | |||||||
chr7:152793166 | T | C | 59 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.101-7365T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793166 | |||||||
chr7:152793174 | C | CT | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.101-7347dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793174 | ||||||
chr7:152793201 | G | GT | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.101-7327dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793201 | ||||||
chr7:152793296 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-7235A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793296 | |||||||
chr7:152793328 | GT | G | 223 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(224): Show |
intron_variant | MODIFIER | c.101-7190delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152793328 | ||||||
chr7:152793329 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101-7202T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793329 | |||||||
chr7:152793363 | C | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-7168C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793363 | |||||||
chr7:152793490 | T | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0067 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.101-7041T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793490 | |||||||
chr7:152793510 | G | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-7021G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793510 | |||||||
chr7:152793552 | G | T | 1 | a0001c0001t0003g0260 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.101-6979G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793552 | |||||||
chr7:152793605 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0250 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-6926T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793605 | |||||||
chr7:152793736 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.101-6795T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793736 | |||||||
chr7:152793884 | A | G | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-6647A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793884 | |||||||
chr7:152793926 | GGAGGAGC others(7): Show |
G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0262 |
3 | HG01167.hp2 HG01169.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.101-6604_101-6591d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793926 | |||||||
chr7:152793952 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-6579T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152793952 | |||||||
chr7:152794109 | T | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0073 |
2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.101-6422T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794109 | |||||||
chr7:152794222 | A | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0067 others(1): Show |
4 | HG02280.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-6309A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794222 | |||||||
chr7:152794385 | G | T | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(237): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.101-6146G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794385 | |||||||
chr7:152794461 | C | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-6070C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794461 | |||||||
chr7:152794561 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5970C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794561 | |||||||
chr7:152794722 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5809A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794722 | |||||||
chr7:152794750 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-5781G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794750 | |||||||
chr7:152794768 | G | C | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-5763G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794768 | |||||||
chr7:152794793 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5738A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794793 | |||||||
chr7:152794830 | C | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-5701C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794830 | |||||||
chr7:152794925 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.101-5606A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794925 | |||||||
chr7:152794954 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.101-5577C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152794954 | |||||||
chr7:152795031 | A | ACT | 108 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(105): Show |
109 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.101-5495_101-5494d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795031 | ||||||
chr7:152795036 | C | CTT | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-5480_101-5479d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795036 | ||||||
chr7:152795036 | CT | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0199 a0001c0001t0001g0223 others(3): Show |
6 | HG01167.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-5479delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795036 | ||||||
chr7:152795037 | T | TC | 7 | a0001c0001t0001g0240 a0001c0001t0001g0259 a0001c0001t0002g0077 others(4): Show |
7 | HG00558.hp1 HG01167.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-5494_101-5493i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795037 | |||||||
chr7:152795042 | T | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-5489T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795042 | |||||||
chr7:152795319 | T | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-5212T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795319 | |||||||
chr7:152795580 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-4951G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795580 | |||||||
chr7:152795603 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-4928C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795603 | |||||||
chr7:152795771 | T | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4760T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795771 | |||||||
chr7:152795846 | G | GT | 103 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0184 others(100): Show |
105 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.101-4671dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152795846 | ||||||
chr7:152795866 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.101-4665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152795866 | |||||||
chr7:152796073 | G | C | 1 | a0001c0001t0002g0082 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.101-4458G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796073 | |||||||
chr7:152796140 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4391C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796140 | |||||||
chr7:152796154 | C | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-4377C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796154 | |||||||
chr7:152796183 | C | T | 2 | a0001c0001t0006g0271 a0001c0001t0006g0283 |
2 | NA18948.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.101-4348C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796183 | |||||||
chr7:152796303 | A | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-4228A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796303 | |||||||
chr7:152796380 | A | T | 1 | a0001c0001t0002g0009 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.101-4151A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796380 | |||||||
chr7:152796421 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.101-4110G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796421 | |||||||
chr7:152796431 | A | G | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-4100A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796431 | |||||||
chr7:152796447 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-4084A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796447 | |||||||
chr7:152796450 | A | G | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-4081A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796450 | |||||||
chr7:152796550 | A | G | 1 | a0001c0001t0002g0008 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.101-3981A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796550 | |||||||
chr7:152796644 | A | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-3887A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796644 | |||||||
chr7:152796716 | G | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-3815G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796716 | |||||||
chr7:152796731 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-3800T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796731 | |||||||
chr7:152796812 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.101-3719C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796812 | |||||||
chr7:152796860 | GT | G | 19 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0148 others(16): Show |
19 | HG00423.hp2 HG00597.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-3633delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTT | G | 76 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0120 others(73): Show |
77 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.101-3634_101-3633d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTTT | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(87): Show |
93 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.101-3635_101-3633d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTTTT | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0181 a0001c0001t0001g0182 others(98): Show |
102 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.101-3636_101-3633d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTTTTTTT others(8): Show |
G | 1 | a0001c0002t0001g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.101-3647_101-3633d others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-3655_101-3633d others(25): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796860 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0006g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.101-3656_101-3633d others(26): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152796860 | ||||||
chr7:152796862 | T | G | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG01952.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.101-3669T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796862 | |||||||
chr7:152796863 | T | G | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-3668T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796863 | |||||||
chr7:152796864 | T | G | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.101-3667T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796864 | |||||||
chr7:152796871 | T | G | 13 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0123 others(10): Show |
13 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-3660T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796871 | |||||||
chr7:152796872 | T | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0122 others(22): Show |
26 | HG00642.hp2 HG01074.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.101-3659T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796872 | |||||||
chr7:152796874 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.101-3657T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796874 | |||||||
chr7:152796875 | T | G | 13 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0216 others(10): Show |
13 | HG00099.hp1 HG00423.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-3656T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796875 | |||||||
chr7:152796876 | T | G | 59 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0186 others(56): Show |
60 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.101-3655T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796876 | |||||||
chr7:152796877 | T | G | 28 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(25): Show |
29 | HG01070.hp1 HG01074.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.101-3654T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796877 | |||||||
chr7:152796878 | T | G | 6 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0272 others(3): Show |
6 | HG02615.hp1 HG02723.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-3653T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796878 | |||||||
chr7:152796879 | T | G | 25 | a0001c0001t0001g0222 a0001c0001t0001g0269 a0001c0001t0001g0270 others(22): Show |
25 | HG00423.hp1 HG01109.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-3652T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796879 | |||||||
chr7:152796880 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(98): Show |
102 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.101-3651T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796880 | |||||||
chr7:152796881 | T | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0086 |
2 | HG01081.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.101-3650T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796881 | |||||||
chr7:152796883 | T | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3648T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796883 | |||||||
chr7:152796884 | T | G | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02074.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.101-3647T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796884 | |||||||
chr7:152796885 | T | G | 3 | a0001c0001t0001g0240 a0001c0001t0002g0030 a0001c0001t0002g0069 |
3 | HG01256.hp2 HG02572.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-3646T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796885 | |||||||
chr7:152796886 | T | G | 1 | a0001c0001t0001g0279 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.101-3645T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796886 | |||||||
chr7:152796907 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.101-3624G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152796907 | |||||||
chr7:152797062 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.101-3469T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797062 | |||||||
chr7:152797101 | A | T | 7 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
8 | HG00741.hp1 HG01074.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-3430A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797101 | |||||||
chr7:152797216 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-3315A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797216 | |||||||
chr7:152797357 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3174G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797357 | |||||||
chr7:152797460 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-3071T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797460 | |||||||
chr7:152797476 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-3055G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797476 | |||||||
chr7:152797573 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.101-2958A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797573 | |||||||
chr7:152797580 | G | A | 4 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0179 others(1): Show |
5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-2951G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797580 | |||||||
chr7:152797643 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-2888T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797643 | |||||||
chr7:152797866 | C | CTT | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-2656_101-2655d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152797866 | ||||||
chr7:152797892 | A | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2639A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152797892 | |||||||
chr7:152798199 | C | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.101-2332C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798199 | |||||||
chr7:152798442 | G | A | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-2089G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798442 | |||||||
chr7:152798583 | T | TCCAAAAA others(9): Show |
1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.101-1944_101-1929d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152798583 | ||||||
chr7:152798847 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.101-1684T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152798847 | |||||||
chr7:152799126 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-1405T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799126 | |||||||
chr7:152799295 | G | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.101-1236G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799295 | |||||||
chr7:152799314 | C | A | 18 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-1217C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799314 | |||||||
chr7:152799507 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-1024C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799507 | |||||||
chr7:152799511 | AATT | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-1009_101-1007d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152799511 | ||||||
chr7:152799534 | T | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.101-997T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799534 | |||||||
chr7:152799541 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-990C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799541 | |||||||
chr7:152799561 | T | TA | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.101-967dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152799561 | ||||||
chr7:152799571 | G | T | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.101-960G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799571 | |||||||
chr7:152799581 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-950T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799581 | |||||||
chr7:152799594 | A | G | 3 | a0001c0001t0002g0042 a0001c0001t0002g0090 a0001c0001t0002g0095 |
3 | NA18956.hp2 NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.101-937A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799594 | |||||||
chr7:152799595 | T | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.101-936T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799595 | |||||||
chr7:152799630 | A | G | 57 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(54): Show |
57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.101-901A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799630 | |||||||
chr7:152799701 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.101-830G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799701 | |||||||
chr7:152799773 | A | G | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-758A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799773 | |||||||
chr7:152799890 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-641A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152799890 | |||||||
chr7:152800064 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-467T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800064 | |||||||
chr7:152800314 | C | A | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.101-217C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800314 | |||||||
chr7:152800323 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.101-208A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 2/11 | chr7 | 152800323 | |||||||
chr7:152800758 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.225+103A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800758 | |||||||
chr7:152800816 | T | TA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.225+162dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152800816 | ||||||
chr7:152800885 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.225+230G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800885 | |||||||
chr7:152800891 | C | T | 59 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.225+236C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152800891 | |||||||
chr7:152801014 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.225+359T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801014 | |||||||
chr7:152801023 | T | C | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+368T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801023 | |||||||
chr7:152801121 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.225+466C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801121 | |||||||
chr7:152801143 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.226-478C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801143 | |||||||
chr7:152801226 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.226-395C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801226 | |||||||
chr7:152801278 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.226-343C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801278 | |||||||
chr7:152801297 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.226-324T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801297 | |||||||
chr7:152801345 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226-276G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801345 | |||||||
chr7:152801348 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.226-273G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801348 | |||||||
chr7:152801466 | T | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.226-155T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 3/11 | chr7 | 152801466 | |||||||
chr7:152801899 | A | AG | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.336+171dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152801899 | ||||||
chr7:152801935 | A | T | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.336+204A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152801935 | |||||||
chr7:152801993 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.336+262G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152801993 | |||||||
chr7:152802279 | A | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.336+548A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802279 | |||||||
chr7:152802409 | T | C | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.336+678T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802409 | |||||||
chr7:152802463 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+732G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802463 | |||||||
chr7:152802737 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(91): Show |
95 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.336+1006G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802737 | |||||||
chr7:152802888 | C | T | 6 | a0001c0001t0001g0125 a0001c0001t0001g0131 a0001c0001t0001g0133 others(3): Show |
6 | HG00544.hp2 HG02074.hp1 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+1157C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802888 | |||||||
chr7:152802968 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+1237A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152802968 | |||||||
chr7:152803127 | G | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.336+1396G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803127 | |||||||
chr7:152803128 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.336+1397C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803128 | |||||||
chr7:152803178 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1447T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803178 | |||||||
chr7:152803217 | A | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1486A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803217 | |||||||
chr7:152803218 | A | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+1487A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803218 | |||||||
chr7:152803248 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+1517A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803248 | |||||||
chr7:152803299 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+1568T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803299 | |||||||
chr7:152803602 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.336+1871G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803602 | |||||||
chr7:152803854 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+2123A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803854 | |||||||
chr7:152803928 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+2197G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152803928 | |||||||
chr7:152804146 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.336+2415G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804146 | |||||||
chr7:152804229 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.336+2498C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804229 | |||||||
chr7:152804286 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.336+2555G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804286 | |||||||
chr7:152804286 | G | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0167 |
2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.336+2555G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804286 | |||||||
chr7:152804574 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.336+2843G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804574 | |||||||
chr7:152804592 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.336+2861G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804592 | |||||||
chr7:152804740 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+3009G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804740 | |||||||
chr7:152804791 | G | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.336+3060G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804791 | |||||||
chr7:152804835 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3104C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804835 | |||||||
chr7:152804882 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.336+3151C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804882 | |||||||
chr7:152804893 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+3162A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804893 | |||||||
chr7:152804986 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.336+3255C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152804986 | |||||||
chr7:152805003 | ACTCATGG others(8): Show |
A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+3274_336+3288d others(17): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805003 | ||||||
chr7:152805020 | G | A | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.336+3289G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805020 | |||||||
chr7:152805051 | G | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+3320G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805051 | |||||||
chr7:152805109 | TG | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+3382delG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805109 | ||||||
chr7:152805112 | G | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.336+3381G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805112 | |||||||
chr7:152805140 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0264 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.336+3409T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805140 | |||||||
chr7:152805476 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.336+3745C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805476 | |||||||
chr7:152805480 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.336+3749C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805480 | |||||||
chr7:152805514 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.336+3783A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805514 | |||||||
chr7:152805622 | A | C | 57 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(54): Show |
57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.336+3891A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805622 | |||||||
chr7:152805803 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.336+4072C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152805803 | |||||||
chr7:152805937 | GGGTT | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+4211_336+4214d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152805937 | ||||||
chr7:152806059 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.336+4328A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806059 | |||||||
chr7:152806091 | T | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(91): Show |
95 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.336+4360T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806091 | |||||||
chr7:152806148 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+4417C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806148 | |||||||
chr7:152806183 | T | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+4452T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806183 | |||||||
chr7:152806408 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.336+4677C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806408 | |||||||
chr7:152806415 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.336+4684G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806415 | |||||||
chr7:152806545 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.336+4814C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806545 | |||||||
chr7:152806581 | T | G | 58 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(55): Show |
58 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.336+4850T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806581 | |||||||
chr7:152806671 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.336+4940C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806671 | |||||||
chr7:152806672 | A | AAGTCTAC others(6): Show |
12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+4949_336+4961d others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152806672 | ||||||
chr7:152806692 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.336+4961C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806692 | |||||||
chr7:152806927 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.336+5196T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152806927 | |||||||
chr7:152807218 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.336+5487T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807218 | |||||||
chr7:152807326 | A | G | 2 | a0001c0001t0002g0028 a0001c0001t0002g0067 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.336+5595A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807326 | |||||||
chr7:152807472 | A | G | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.336+5741A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807472 | |||||||
chr7:152807619 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+5888C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807619 | |||||||
chr7:152807806 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.336+6075G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152807806 | |||||||
chr7:152808171 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.337-6379A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808171 | |||||||
chr7:152808247 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.337-6303C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808247 | |||||||
chr7:152808311 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.337-6239T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808311 | |||||||
chr7:152808376 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337-6174A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808376 | |||||||
chr7:152808433 | C | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.337-6117C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808433 | |||||||
chr7:152808565 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.337-5985A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808565 | |||||||
chr7:152808609 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.337-5941C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808609 | |||||||
chr7:152808986 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-5564T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152808986 | |||||||
chr7:152809052 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.337-5498G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809052 | |||||||
chr7:152809099 | G | A | 4 | a0001c0001t0002g0042 a0001c0001t0002g0090 a0001c0001t0002g0095 others(1): Show |
4 | NA18956.hp2 NA19062.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-5451G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809099 | |||||||
chr7:152809284 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-5266C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809284 | |||||||
chr7:152809306 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0289 others(3): Show |
7 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.337-5244A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809306 | |||||||
chr7:152809404 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.337-5146G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809404 | |||||||
chr7:152809547 | T | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0183 others(114): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-5003T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809547 | |||||||
chr7:152809583 | C | A | 1 | a0001c0001t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.337-4967C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809583 | |||||||
chr7:152809634 | C | T | 4 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0179 others(1): Show |
5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-4916C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809634 | |||||||
chr7:152809646 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-4904A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809646 | |||||||
chr7:152809688 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.337-4862A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809688 | |||||||
chr7:152809774 | C | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.337-4776C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809774 | |||||||
chr7:152809785 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-4765C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809785 | |||||||
chr7:152809812 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.337-4738A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152809812 | |||||||
chr7:152809915 | CT | C | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.337-4625delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152809915 | ||||||
chr7:152810014 | A | C | 2 | a0001c0001t0002g0158 a0001c0001t0002g0167 |
2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.337-4536A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810014 | |||||||
chr7:152810065 | C | T | 12 | a0001c0001t0001g0184 a0001c0001t0001g0220 a0001c0001t0001g0221 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.337-4485C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810065 | |||||||
chr7:152810066 | G | A | 1 | a0001c0001t0009g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.337-4484G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810066 | |||||||
chr7:152810138 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.337-4412C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810138 | |||||||
chr7:152810263 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.337-4287C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810263 | |||||||
chr7:152810271 | T | C | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.337-4279T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810271 | |||||||
chr7:152810273 | A | G | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.337-4277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810273 | |||||||
chr7:152810364 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-4186C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810364 | |||||||
chr7:152810408 | G | GT | 28 | a0001c0001t0001g0013 a0001c0001t0001g0113 a0001c0001t0001g0115 others(25): Show |
28 | HG00597.hp1 HG00642.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.337-4122dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810408 | ||||||
chr7:152810420 | T | TG | 7 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0289 others(4): Show |
8 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-4130_337-4129i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810420 | |||||||
chr7:152810423 | T | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0190 a0001c0001t0001g0228 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-4127T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810423 | |||||||
chr7:152810423 | T | TG | 13 | a0001c0001t0001g0291 a0001c0001t0002g0055 a0001c0001t0002g0063 others(10): Show |
13 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.337-4127_337-4126i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810423 | |||||||
chr7:152810426 | T | G | 93 | a0001c0001t0001g0005 a0001c0001t0001g0181 a0001c0001t0001g0182 others(90): Show |
94 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.337-4124T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810426 | |||||||
chr7:152810426 | T | TG | 107 | a0001c0001t0001g0004 a0001c0001t0001g0185 a0001c0001t0001g0188 others(104): Show |
109 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.337-4124_337-4123i others(3): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810426 | |||||||
chr7:152810426 | T | TTG | 24 | a0001c0001t0001g0258 a0001c0001t0001g0300 a0001c0001t0002g0002 others(21): Show |
25 | HG00423.hp1 HG00558.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.337-4123_337-4122i others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810426 | ||||||
chr7:152810429 | G | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-4121G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810429 | |||||||
chr7:152810481 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.337-4069A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810481 | |||||||
chr7:152810524 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-4026C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810524 | |||||||
chr7:152810588 | G | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.337-3962G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810588 | |||||||
chr7:152810683 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.337-3867C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810683 | |||||||
chr7:152810745 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-3805T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810745 | |||||||
chr7:152810903 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(12): Show |
15 | HG01099.hp2 HG01106.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.337-3629dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810903 | ||||||
chr7:152810903 | CA | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0131 a0001c0001t0001g0150 others(10): Show |
14 | HG00544.hp2 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.337-3629delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152810903 | ||||||
chr7:152810969 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.337-3581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152810969 | |||||||
chr7:152811372 | G | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-3178G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811372 | |||||||
chr7:152811462 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.337-3088C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811462 | |||||||
chr7:152811580 | C | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-2970C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811580 | |||||||
chr7:152811586 | A | G | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-2964A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811586 | |||||||
chr7:152811955 | A | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-2595A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152811955 | |||||||
chr7:152812019 | C | CTTTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0249 a0001c0001t0001g0289 others(3): Show |
7 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-2505_337-2502d others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTT | 8 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0290 others(5): Show |
8 | HG01074.hp2 HG02055.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-2506_337-2502d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTT | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
6 | HG00735.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-2507_337-2502d others(8): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT | 22 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0201 others(19): Show |
22 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.337-2508_337-2502d others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(1): Show |
25 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(22): Show |
25 | HG00423.hp2 HG01071.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.337-2509_337-2502d others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0203 others(5): Show |
8 | HG00597.hp2 HG02027.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-2510_337-2502d others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0184 a0001c0001t0001g0235 |
2 | HG02258.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.337-2511_337-2502d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0207 a0001c0001t0001g0215 a0001c0001t0001g0221 others(1): Show |
4 | HG00642.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-2512_337-2502d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0174 a0001c0001t0003g0268 |
2 | HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.337-2513_337-2502d others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0168 a0001c0001t0003g0260 a0001c0001t0004g0171 |
3 | HG02486.hp2 HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.337-2514_337-2502d others(15): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0004g0172 a0001c0001t0004g0176 |
2 | HG01891.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.337-2515_337-2502d others(16): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CT | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0112 others(39): Show |
44 | HG00438.hp2 HG00741.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.337-2502delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CTT | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0200 others(3): Show |
6 | HG01952.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-2503_337-2502d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CTTTTTTT others(1): Show |
C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(86): Show |
90 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.337-2509_337-2502d others(10): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CTTTTTTT others(2): Show |
C | 27 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0026 others(24): Show |
27 | HG00099.hp1 HG00738.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.337-2510_337-2502d others(11): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CTTTTTTT others(3): Show |
C | 16 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(13): Show |
16 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.337-2511_337-2502d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812019 | CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0177 others(1): Show |
4 | HG01361.hp2 HG01934.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.337-2517_337-2502d others(18): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812019 | ||||||
chr7:152812034 | T | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-2516T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812034 | |||||||
chr7:152812054 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.337-2496G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812054 | |||||||
chr7:152812061 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-2489T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812061 | |||||||
chr7:152812064 | T | A | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.337-2486T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812064 | |||||||
chr7:152812093 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-2457C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812093 | |||||||
chr7:152812126 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-2424G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812126 | |||||||
chr7:152812149 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.337-2401G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812149 | |||||||
chr7:152812196 | A | G | 17 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0026 others(14): Show |
17 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-2354A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812196 | |||||||
chr7:152812228 | A | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(118): Show |
123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.337-2322A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812228 | |||||||
chr7:152812238 | T | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(118): Show |
123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.337-2312T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812238 | |||||||
chr7:152812273 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.337-2277C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812273 | |||||||
chr7:152812320 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-2230C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812320 | |||||||
chr7:152812349 | C | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-2201C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812349 | |||||||
chr7:152812353 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(123): Show |
128 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.337-2197A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812353 | |||||||
chr7:152812377 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.337-2173T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812377 | |||||||
chr7:152812454 | A | T | 1 | a0001c0001t0002g0036 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.337-2096A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812454 | |||||||
chr7:152812537 | G | GT | 27 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(24): Show |
28 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.337-2004dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152812537 | ||||||
chr7:152812566 | A | G | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-1984A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812566 | |||||||
chr7:152812602 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.337-1948T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812602 | |||||||
chr7:152812611 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.337-1939G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812611 | |||||||
chr7:152812843 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0182 a0001c0001t0001g0183 others(115): Show |
119 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.337-1707G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812843 | |||||||
chr7:152812874 | G | T | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(242): Show |
248 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.337-1676G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812874 | |||||||
chr7:152812899 | TC | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0183 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.337-1650delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152812899 | |||||||
chr7:152813406 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1144G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813406 | |||||||
chr7:152813420 | T | C | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1130T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813420 | |||||||
chr7:152813421 | G | C | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1129G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813421 | |||||||
chr7:152813435 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1115C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813435 | |||||||
chr7:152813438 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(112): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.337-1112T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813438 | |||||||
chr7:152813455 | A | G | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.337-1095A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813455 | |||||||
chr7:152813493 | C | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-1057C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813493 | |||||||
chr7:152813516 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.337-1034A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813516 | |||||||
chr7:152813529 | TA | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(112): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.337-1020delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813529 | |||||||
chr7:152813613 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-937C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813613 | |||||||
chr7:152813667 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.337-883A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813667 | |||||||
chr7:152813670 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337-880G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813670 | |||||||
chr7:152813831 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-719G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813831 | |||||||
chr7:152813865 | CTTTTCTC others(2): Show |
C | 13 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0009 others(10): Show |
14 | HG01074.hp2 HG01099.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.337-683_337-675del others(9): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 152813865 | ||||||
chr7:152813939 | C | T | 6 | a0001c0001t0001g0183 a0001c0001t0002g0070 a0001c0001t0002g0071 others(3): Show |
6 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-611C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152813939 | |||||||
chr7:152814042 | C | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0093 |
2 | NA18957.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.337-508C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814042 | |||||||
chr7:152814111 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.337-439C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814111 | |||||||
chr7:152814202 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.337-348G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814202 | |||||||
chr7:152814206 | T | G | 24 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(21): Show |
24 | HG01074.hp2 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.337-344T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814206 | |||||||
chr7:152814257 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(114): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.337-293G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814257 | |||||||
chr7:152814274 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.337-276C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814274 | |||||||
chr7:152814389 | T | C | 289 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
294 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(291): Show |
intron_variant | MODIFIER | c.337-161T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814389 | |||||||
chr7:152814513 | C | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.337-37C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814513 | |||||||
chr7:152814531 | A | G | 8 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0030 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-19A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 4/11 | chr7 | 152814531 | |||||||
chr7:152814696 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+51C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814696 | |||||||
chr7:152814772 | C | T | 10 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(7): Show |
11 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814772 | |||||||
chr7:152814976 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+331C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152814976 | |||||||
chr7:152815208 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.432+563A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815208 | |||||||
chr7:152815295 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+650C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815295 | |||||||
chr7:152815310 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815310 | |||||||
chr7:152815363 | T | C | 57 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(54): Show |
57 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.432+718T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815363 | |||||||
chr7:152815373 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+728C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815373 | |||||||
chr7:152815468 | G | A | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(237): Show |
244 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.432+823G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815468 | |||||||
chr7:152815544 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.432+899G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815544 | |||||||
chr7:152815571 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.433-910G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815571 | |||||||
chr7:152815621 | G | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.433-860G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815621 | |||||||
chr7:152815666 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-815G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815666 | |||||||
chr7:152815951 | C | T | 242 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(239): Show |
245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.433-530C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815951 | |||||||
chr7:152815979 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.433-502C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152815979 | |||||||
chr7:152816032 | G | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.433-449G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816032 | |||||||
chr7:152816089 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-392C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816089 | |||||||
chr7:152816169 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0228 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.433-312A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816169 | |||||||
chr7:152816284 | A | C | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-197A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816284 | |||||||
chr7:152816384 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.433-97T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816384 | |||||||
chr7:152816455 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-26G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816455 | |||||||
chr7:152816477 | C | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.433-4C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 5/11 | chr7 | 152816477 | |||||||
chr7:152816638 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.540+50C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816638 | |||||||
chr7:152816655 | T | TA | 8 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG00609.hp1 HG01099.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.540+81dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152816655 | ||||||
chr7:152816684 | G | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.540+96G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816684 | |||||||
chr7:152816754 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540+166A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816754 | |||||||
chr7:152816769 | G | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.540+181G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816769 | |||||||
chr7:152816780 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.540+192A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816780 | |||||||
chr7:152816846 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0298 |
2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.540+258A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816846 | |||||||
chr7:152816874 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.540+286G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816874 | |||||||
chr7:152816907 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+319C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816907 | |||||||
chr7:152816908 | G | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(90): Show |
94 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.540+320G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816908 | |||||||
chr7:152816910 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0216 a0001c0001t0001g0217 others(12): Show |
16 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.540+322G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816910 | |||||||
chr7:152816937 | T | C | 148 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.540+349T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816937 | |||||||
chr7:152816970 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.540+382C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152816970 | |||||||
chr7:152817074 | T | C | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+486T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817074 | |||||||
chr7:152817112 | C | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.540+524C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817112 | |||||||
chr7:152817122 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.540+534C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817122 | |||||||
chr7:152817295 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540+707C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817295 | |||||||
chr7:152817575 | G | A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+987G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817575 | |||||||
chr7:152817610 | T | G | 157 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(154): Show |
159 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.540+1022T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817610 | |||||||
chr7:152817638 | TCTC | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | NA18951.hp1 NA19007.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+1057_540+1059d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152817638 | ||||||
chr7:152817714 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540+1126G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817714 | |||||||
chr7:152817984 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+1396G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152817984 | |||||||
chr7:152818172 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.540+1584G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818172 | |||||||
chr7:152818254 | CA | C | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+1667delA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818254 | |||||||
chr7:152818330 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.540+1742G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818330 | |||||||
chr7:152818341 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.540+1753A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818341 | |||||||
chr7:152818409 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.540+1821A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818409 | |||||||
chr7:152818456 | CT | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.541-1833delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152818456 | ||||||
chr7:152818533 | C | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1766C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818533 | |||||||
chr7:152818547 | T | G | 5 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0001g0276 others(2): Show |
5 | NA18942.hp1 NA18955.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-1752T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818547 | |||||||
chr7:152818568 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.541-1731G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818568 | |||||||
chr7:152818777 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-1522C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818777 | |||||||
chr7:152818876 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(112): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.541-1423G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152818876 | |||||||
chr7:152819022 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-1277A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819022 | |||||||
chr7:152819279 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(149): Show |
154 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.541-1020G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819279 | |||||||
chr7:152819320 | C | T | 29 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(26): Show |
29 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.541-979C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819320 | |||||||
chr7:152819386 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.541-913C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819386 | |||||||
chr7:152819474 | A | G | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.541-825A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819474 | |||||||
chr7:152819523 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-776C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819523 | |||||||
chr7:152819610 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-689G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819610 | |||||||
chr7:152819894 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0255 |
2 | HG00609.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.541-405G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819894 | |||||||
chr7:152819987 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-312C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152819987 | |||||||
chr7:152820132 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.541-167T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820132 | |||||||
chr7:152820170 | G | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.541-129G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820170 | |||||||
chr7:152820256 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.541-43C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 6/11 | chr7 | 152820256 | |||||||
chr7:152820639 | T | C | 153 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
155 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.684+197T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820639 | |||||||
chr7:152820769 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+327C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820769 | |||||||
chr7:152820792 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.684+350A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820792 | |||||||
chr7:152820809 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.684+367C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820809 | |||||||
chr7:152820897 | C | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.684+455C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820897 | |||||||
chr7:152820978 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+536C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152820978 | |||||||
chr7:152821075 | T | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+633T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821075 | |||||||
chr7:152821079 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0287 others(6): Show |
10 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.684+637G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821079 | |||||||
chr7:152821135 | C | T | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.684+693C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821135 | |||||||
chr7:152821161 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
5 | HG01109.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.684+719G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821161 | |||||||
chr7:152821199 | T | A | 17 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+757T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821199 | |||||||
chr7:152821309 | C | T | 1 | a0001c0001t0009g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.684+867C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821309 | |||||||
chr7:152821332 | A | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+890A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821332 | |||||||
chr7:152821472 | G | GA | 24 | a0001c0001t0001g0115 a0001c0001t0001g0216 a0001c0001t0001g0217 others(21): Show |
24 | HG00735.hp1 HG01109.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.684+1043dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152821472 | ||||||
chr7:152821532 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.684+1090C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821532 | |||||||
chr7:152821567 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.684+1125A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821567 | |||||||
chr7:152821641 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(69): Show |
73 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.684+1199A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821641 | |||||||
chr7:152821840 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.684+1398C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821840 | |||||||
chr7:152821872 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.684+1430T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821872 | |||||||
chr7:152821992 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.685-1350A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152821992 | |||||||
chr7:152822083 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.685-1259G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822083 | |||||||
chr7:152822171 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-1171C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822171 | |||||||
chr7:152822306 | C | T | 133 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(130): Show |
135 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.685-1036C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822306 | |||||||
chr7:152822328 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-1014G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822328 | |||||||
chr7:152822363 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.685-979C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822363 | |||||||
chr7:152822460 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-882C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822460 | |||||||
chr7:152822556 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-786C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822556 | |||||||
chr7:152822677 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-665C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822677 | |||||||
chr7:152822955 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.685-387C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822955 | |||||||
chr7:152822956 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0282 |
2 | NA18939.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.685-386G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152822956 | |||||||
chr7:152823001 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0286 others(7): Show |
11 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.685-341C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823001 | |||||||
chr7:152823028 | G | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.685-314G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823028 | |||||||
chr7:152823080 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.685-262C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823080 | |||||||
chr7:152823181 | A | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-161A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823181 | |||||||
chr7:152823190 | T | C | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-152T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823190 | |||||||
chr7:152823221 | T | TA | 21 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(18): Show |
21 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.685-120dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152823221 | ||||||
chr7:152823303 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0001g0212 a0001c0001t0001g0213 others(3): Show |
6 | HG00597.hp2 HG00609.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.685-39G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 7/11 | chr7 | 152823303 | |||||||
chr7:152823621 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.858+106C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823621 | |||||||
chr7:152823646 | T | C | 155 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0014 others(152): Show |
157 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.858+131T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823646 | |||||||
chr7:152823650 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.858+135C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823650 | |||||||
chr7:152823757 | A | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.858+242A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823757 | |||||||
chr7:152823803 | GT | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+289delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823803 | |||||||
chr7:152823855 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.858+340C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823855 | |||||||
chr7:152823899 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.858+384G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823899 | |||||||
chr7:152823950 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.858+435A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152823950 | |||||||
chr7:152824412 | A | G | 21 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(18): Show |
21 | HG01074.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.859-618A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824412 | |||||||
chr7:152824418 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.859-612A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824418 | |||||||
chr7:152824864 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-166G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824864 | |||||||
chr7:152824868 | T | A | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.859-162T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 8/11 | chr7 | 152824868 | |||||||
chr7:152825304 | T | TTTTTA | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+202_951+206dup others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152825304 | ||||||
chr7:152825335 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+213G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825335 | |||||||
chr7:152825354 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+232C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825354 | |||||||
chr7:152825505 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+383C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825505 | |||||||
chr7:152825538 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.951+416A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825538 | |||||||
chr7:152825759 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+637C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825759 | |||||||
chr7:152825816 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+694C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825816 | |||||||
chr7:152825881 | A | T | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.951+759A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152825881 | |||||||
chr7:152826026 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.951+904A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826026 | |||||||
chr7:152826064 | G | T | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.951+942G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826064 | |||||||
chr7:152826149 | G | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+1027G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826149 | |||||||
chr7:152826197 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.951+1075T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826197 | |||||||
chr7:152826360 | CTT | C | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+1241_951+1242d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152826360 | ||||||
chr7:152826481 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+1359T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826481 | |||||||
chr7:152826555 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.951+1433T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826555 | |||||||
chr7:152826928 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+1806C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152826928 | |||||||
chr7:152827012 | C | G | 94 | a0001c0001t0001g0004 a0001c0001t0001g0196 a0001c0001t0001g0197 others(91): Show |
95 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.951+1890C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827012 | |||||||
chr7:152827043 | G | A | 6 | a0001c0001t0001g0133 a0001c0001t0001g0300 a0001c0001t0002g0002 others(3): Show |
7 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.951+1921G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827043 | |||||||
chr7:152827063 | C | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+1941C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827063 | |||||||
chr7:152827063 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.951+1941C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827063 | |||||||
chr7:152827107 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.951+1985A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827107 | |||||||
chr7:152827108 | A | G | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+1986A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827108 | |||||||
chr7:152827282 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2160G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827282 | |||||||
chr7:152827288 | G | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+2166G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827288 | |||||||
chr7:152827307 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.951+2185C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827307 | |||||||
chr7:152827415 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.951+2293T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827415 | |||||||
chr7:152827486 | T | G | 1 | a0001c0001t0001g0291 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.951+2364T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827486 | |||||||
chr7:152827503 | T | C | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+2381T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827503 | |||||||
chr7:152827533 | C | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+2411C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827533 | |||||||
chr7:152827544 | G | T | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.951+2422G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827544 | |||||||
chr7:152827699 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+2577C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827699 | |||||||
chr7:152827855 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.951+2733C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827855 | |||||||
chr7:152827896 | GT | G | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2782delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152827896 | ||||||
chr7:152827958 | A | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+2836A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152827958 | |||||||
chr7:152828160 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(90): Show |
94 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.951+3038T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828160 | |||||||
chr7:152828184 | T | C | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+3062T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828184 | |||||||
chr7:152828197 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.951+3075T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828197 | |||||||
chr7:152828206 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.951+3084G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828206 | |||||||
chr7:152828276 | C | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+3154C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828276 | |||||||
chr7:152828344 | C | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(112): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.951+3222C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828344 | |||||||
chr7:152828353 | T | G | 59 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.951+3231T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828353 | |||||||
chr7:152828360 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.951+3238T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828360 | |||||||
chr7:152828367 | T | C | 1 | a0001c0001t0002g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.951+3245T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828367 | |||||||
chr7:152828451 | G | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3329G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828451 | |||||||
chr7:152828518 | G | A | 1 | a0001c0001t0009g0143 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.951+3396G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828518 | |||||||
chr7:152828580 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.951+3458C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828580 | |||||||
chr7:152828643 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.951+3521C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828643 | |||||||
chr7:152828644 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+3522G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828644 | |||||||
chr7:152828674 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.951+3552C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828674 | |||||||
chr7:152828688 | T | A | 1 | a0001c0001t0001g0303 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.951+3566T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828688 | |||||||
chr7:152828737 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.951+3615G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828737 | |||||||
chr7:152828772 | C | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0094 |
2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.951+3650C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828772 | |||||||
chr7:152828811 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+3689A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828811 | |||||||
chr7:152828975 | T | G | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.951+3853T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152828975 | |||||||
chr7:152829032 | T | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3910T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829032 | |||||||
chr7:152829034 | G | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3912G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829034 | |||||||
chr7:152829035 | T | G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3913T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829035 | |||||||
chr7:152829036 | G | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3914G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829036 | |||||||
chr7:152829040 | GTGTGTAT others(19): Show |
G | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+3919_951+3944d others(28): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829040 | |||||||
chr7:152829044 | G | GTGTA | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+3923_951+3924i others(6): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829044 | ||||||
chr7:152829055 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.951+3933T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829055 | |||||||
chr7:152829057 | T | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(76): Show |
80 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.951+3935T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829057 | |||||||
chr7:152829057 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.951+3936_951+3937i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | ||||||
chr7:152829057 | T | TATATATA others(3): Show |
14 | a0001c0001t0001g0269 a0001c0001t0001g0272 a0001c0001t0001g0273 others(11): Show |
14 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.951+3936_951+3937i others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | ||||||
chr7:152829057 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0284 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.951+3936_951+3937i others(14): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152829057 | ||||||
chr7:152829059 | C | T | 2 | a0001c0001t0005g0261 a0001c0001t0008g0305 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.951+3937C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829059 | |||||||
chr7:152829061 | C | T | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+3939C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829061 | |||||||
chr7:152829546 | A | G | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.951+4424A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829546 | |||||||
chr7:152829839 | G | A | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+4717G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829839 | |||||||
chr7:152829873 | C | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+4751C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152829873 | |||||||
chr7:152830041 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.951+4919A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830041 | |||||||
chr7:152830462 | G | T | 8 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02486.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.951+5340G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830462 | |||||||
chr7:152830583 | CTG | C | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+5463_951+5464d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152830583 | ||||||
chr7:152830675 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0228 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.951+5553A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830675 | |||||||
chr7:152830758 | T | C | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.951+5636T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830758 | |||||||
chr7:152830893 | T | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+5771T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152830893 | |||||||
chr7:152831022 | G | T | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+5900G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831022 | |||||||
chr7:152831144 | A | T | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+6022A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831144 | |||||||
chr7:152831175 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+6053T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831175 | |||||||
chr7:152831257 | G | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+6135G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831257 | |||||||
chr7:152831288 | A | G | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+6166A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831288 | |||||||
chr7:152831313 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.951+6191C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831313 | |||||||
chr7:152831336 | G | C | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+6214G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831336 | |||||||
chr7:152831359 | AGGGCTGT others(3): Show |
A | 9 | a0001c0001t0001g0184 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
9 | HG02258.hp2 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+6241_951+6250d others(12): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152831359 | ||||||
chr7:152831451 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.951+6329G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831451 | |||||||
chr7:152831466 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.951+6344G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831466 | |||||||
chr7:152831605 | G | A | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+6483G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831605 | |||||||
chr7:152831618 | C | T | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.951+6496C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831618 | |||||||
chr7:152831810 | C | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+6688C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831810 | |||||||
chr7:152831890 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(112): Show |
116 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.951+6768G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152831890 | |||||||
chr7:152832056 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.951+6934A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832056 | |||||||
chr7:152832094 | A | G | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+6972A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832094 | |||||||
chr7:152832140 | C | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+7018C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832140 | |||||||
chr7:152832147 | A | C | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7025A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832147 | |||||||
chr7:152832403 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.951+7281A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832403 | |||||||
chr7:152832429 | C | T | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.951+7307C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832429 | |||||||
chr7:152832479 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+7357G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832479 | |||||||
chr7:152832530 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.951+7408T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832530 | |||||||
chr7:152832612 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0094 |
2 | HG02165.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.951+7490C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832612 | |||||||
chr7:152832778 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7656C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832778 | |||||||
chr7:152832778 | C | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+7656C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832778 | |||||||
chr7:152832779 | G | C | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+7657G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832779 | |||||||
chr7:152832793 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+7671C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832793 | |||||||
chr7:152832901 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+7779A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832901 | |||||||
chr7:152832921 | T | C | 42 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
43 | HG00735.hp1 HG01099.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.951+7799T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832921 | |||||||
chr7:152832987 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.951+7865C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152832987 | |||||||
chr7:152833053 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.951+7931A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833053 | |||||||
chr7:152833173 | G | A | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+8051G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833173 | |||||||
chr7:152833231 | A | G | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.951+8109A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833231 | |||||||
chr7:152833261 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.951+8139G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833261 | |||||||
chr7:152833262 | C | A | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+8140C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833262 | |||||||
chr7:152833264 | G | A | 1 | a0001c0001t0002g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.951+8142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833264 | |||||||
chr7:152833268 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.951+8146A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833268 | |||||||
chr7:152833406 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+8284A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833406 | |||||||
chr7:152833496 | T | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8374T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833496 | |||||||
chr7:152833527 | G | A | 11 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(8): Show |
12 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.951+8405G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833527 | |||||||
chr7:152833533 | G | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0053 a0001c0001t0002g0159 others(2): Show |
6 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+8411G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833533 | |||||||
chr7:152833572 | T | C | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.951+8450T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833572 | |||||||
chr7:152833610 | TAAG | T | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8493_951+8495d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152833610 | ||||||
chr7:152833737 | T | C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8615T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833737 | |||||||
chr7:152833789 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+8667C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833789 | |||||||
chr7:152833800 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.951+8678C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833800 | |||||||
chr7:152833930 | T | C | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.951+8808T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833930 | |||||||
chr7:152833936 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.951+8814G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152833936 | |||||||
chr7:152834092 | T | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+8970T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834092 | |||||||
chr7:152834093 | TTCTAAAT others(4): Show |
T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
19 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.951+8972_951+8982d others(13): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834093 | |||||||
chr7:152834146 | G | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0078 |
3 | HG00544.hp1 HG00741.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.951+9024G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834146 | |||||||
chr7:152834155 | G | GT | 16 | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0001g0181 others(13): Show |
16 | HG00438.hp1 HG00609.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.951+9047dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152834155 | ||||||
chr7:152834155 | G | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+9033G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834155 | |||||||
chr7:152834302 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9180C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834302 | |||||||
chr7:152834406 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0002g0092 a0001c0001t0002g0100 |
3 | HG00438.hp1 HG02071.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.951+9284G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834406 | |||||||
chr7:152834443 | C | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.951+9321C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834443 | |||||||
chr7:152834446 | G | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.951+9324G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834446 | |||||||
chr7:152834563 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.951+9441C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834563 | |||||||
chr7:152834627 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+9505C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834627 | |||||||
chr7:152834628 | T | C | 1 | a0001c0001t0002g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.951+9506T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834628 | |||||||
chr7:152834680 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+9558G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834680 | |||||||
chr7:152834880 | T | G | 1 | a0001c0001t0002g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.951+9758T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834880 | |||||||
chr7:152834946 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9824A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152834946 | |||||||
chr7:152835055 | G | GT | 9 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(6): Show |
10 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.951+9944dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152835055 | ||||||
chr7:152835055 | GT | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.951+9944delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152835055 | ||||||
chr7:152835084 | A | C | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+9962A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835084 | |||||||
chr7:152835201 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.951+10079C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835201 | |||||||
chr7:152835311 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.951+10189G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835311 | |||||||
chr7:152835398 | A | C | 1 | a0001c0001t0002g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.951+10276A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835398 | |||||||
chr7:152835531 | T | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00597.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.951+10409T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835531 | |||||||
chr7:152835671 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.951+10549G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835671 | |||||||
chr7:152835709 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+10587T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835709 | |||||||
chr7:152835834 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.951+10712C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835834 | |||||||
chr7:152835956 | G | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.951+10834G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835956 | |||||||
chr7:152835995 | AC | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+10874delC | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152835995 | |||||||
chr7:152836043 | T | C | 6 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
6 | NA18942.hp2 NA18971.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+10921T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836043 | |||||||
chr7:152836126 | G | A | 4 | a0001c0001t0002g0002 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
5 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+11004G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836126 | |||||||
chr7:152836417 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.951+11295A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836417 | |||||||
chr7:152836429 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.951+11307T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836429 | |||||||
chr7:152836566 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.951+11444G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836566 | |||||||
chr7:152836609 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.951+11487G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836609 | |||||||
chr7:152836615 | T | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+11493T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836615 | |||||||
chr7:152836747 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0099 |
2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.951+11625T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836747 | |||||||
chr7:152836893 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.951+11771G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836893 | |||||||
chr7:152836900 | A | T | 59 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.951+11778A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836900 | |||||||
chr7:152836927 | T | A | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.951+11805T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152836927 | |||||||
chr7:152837175 | C | CA | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+12062dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152837175 | ||||||
chr7:152837181 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.951+12059A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837181 | |||||||
chr7:152837184 | A | C | 1 | a0001c0001t0001g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951+12062A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837184 | |||||||
chr7:152837287 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+12165G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837287 | |||||||
chr7:152837297 | G | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+12175G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837297 | |||||||
chr7:152837567 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.951+12445A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837567 | |||||||
chr7:152837603 | C | A | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.951+12481C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837603 | |||||||
chr7:152837720 | G | T | 1 | a0001c0001t0002g0048 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.951+12598G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837720 | |||||||
chr7:152837765 | C | T | 7 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0300 others(4): Show |
8 | HG02615.hp1 HG02630.hp2 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+12643C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837765 | |||||||
chr7:152837789 | A | G | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.951+12667A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837789 | |||||||
chr7:152837837 | A | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.951+12715A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837837 | |||||||
chr7:152837854 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.951+12732G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837854 | |||||||
chr7:152837912 | C | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(35): Show |
39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.951+12790C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152837912 | |||||||
chr7:152838085 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.951+12963C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838085 | |||||||
chr7:152838342 | A | G | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.951+13220A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838342 | |||||||
chr7:152838374 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.951+13252T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838374 | |||||||
chr7:152838384 | A | G | 74 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.951+13262A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838384 | |||||||
chr7:152838435 | A | T | 1 | a0001c0003t0003g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951+13313A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838435 | |||||||
chr7:152838448 | C | A | 1 | a0001c0001t0007g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.951+13326C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838448 | |||||||
chr7:152838449 | A | C | 1 | a0001c0001t0007g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.951+13327A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838449 | |||||||
chr7:152838808 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-13318A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838808 | |||||||
chr7:152838811 | C | G | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-13315C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838811 | |||||||
chr7:152838823 | T | C | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(224): Show |
230 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.952-13303T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838823 | |||||||
chr7:152838990 | G | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-13136G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152838990 | |||||||
chr7:152839014 | G | T | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0167 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.952-13112G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839014 | |||||||
chr7:152839015 | C | T | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0167 others(1): Show |
4 | HG01074.hp2 HG01099.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.952-13111C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839015 | |||||||
chr7:152839029 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-13097C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839029 | |||||||
chr7:152839129 | A | T | 1 | a0001c0001t0007g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-12997A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839129 | |||||||
chr7:152839146 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.952-12980A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839146 | |||||||
chr7:152839147 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.952-12979G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839147 | |||||||
chr7:152839188 | C | T | 8 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(5): Show |
9 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.952-12938C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839188 | |||||||
chr7:152839196 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.952-12930G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839196 | |||||||
chr7:152839236 | C | T | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.952-12890C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839236 | |||||||
chr7:152839264 | C | CG | 74 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0001g0184 others(71): Show |
75 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.952-12856dupG | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152839264 | ||||||
chr7:152839438 | C | A | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-12688C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839438 | |||||||
chr7:152839453 | C | T | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-12673C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839453 | |||||||
chr7:152839454 | G | C | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-12672G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839454 | |||||||
chr7:152839494 | T | A | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-12632T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839494 | |||||||
chr7:152839531 | T | C | 59 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.952-12595T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839531 | |||||||
chr7:152839648 | C | T | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0296 others(9): Show |
13 | HG01952.hp1 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.952-12478C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839648 | |||||||
chr7:152839659 | C | T | 1 | a0001c0001t0002g0003 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.952-12467C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839659 | |||||||
chr7:152839780 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.952-12346C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839780 | |||||||
chr7:152839781 | A | G | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-12345A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839781 | |||||||
chr7:152839875 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-12251G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839875 | |||||||
chr7:152839887 | A | T | 1 | a0001c0001t0002g0104 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.952-12239A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839887 | |||||||
chr7:152839923 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-12203C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839923 | |||||||
chr7:152839947 | C | A | 1 | a0001c0001t0007g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-12179C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152839947 | |||||||
chr7:152840165 | G | GGGTAGCT others(11): Show |
1 | a0001c0001t0007g0061 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.952-11956_952-1195 others(22): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152840165 | ||||||
chr7:152840175 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-11951A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840175 | |||||||
chr7:152840183 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.952-11943G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840183 | |||||||
chr7:152840315 | C | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-11811C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840315 | |||||||
chr7:152840354 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-11772C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840354 | |||||||
chr7:152840385 | C | T | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
18 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.952-11741C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840385 | |||||||
chr7:152840464 | G | A | 58 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(55): Show |
58 | HG00099.hp2 HG00423.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.952-11662G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840464 | |||||||
chr7:152840480 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11646C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840480 | |||||||
chr7:152840481 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11645T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840481 | |||||||
chr7:152840485 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.952-11641A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840485 | |||||||
chr7:152840494 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.952-11632C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840494 | |||||||
chr7:152840654 | C | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-11472C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840654 | |||||||
chr7:152840747 | C | G | 1 | a0001c0001t0003g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.952-11379C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840747 | |||||||
chr7:152840766 | G | A | 35 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(32): Show |
36 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.952-11360G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840766 | |||||||
chr7:152840768 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.952-11358C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840768 | |||||||
chr7:152840825 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.952-11301C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840825 | |||||||
chr7:152840899 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.952-11227G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840899 | |||||||
chr7:152840963 | C | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-11163C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152840963 | |||||||
chr7:152841057 | A | G | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952-11069A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841057 | |||||||
chr7:152841153 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.952-10973C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841153 | |||||||
chr7:152841542 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.952-10584G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841542 | |||||||
chr7:152841733 | C | T | 1 | a0001c0001t0002g0012 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.952-10393C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841733 | |||||||
chr7:152841777 | T | G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0076 others(2): Show |
5 | HG00423.hp1 HG00558.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-10349T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841777 | |||||||
chr7:152841794 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-10332G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841794 | |||||||
chr7:152841884 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0231 |
2 | NA18948.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.952-10242G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152841884 | |||||||
chr7:152842073 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0248 |
2 | HG01243.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.952-10053G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842073 | |||||||
chr7:152842090 | C | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(35): Show |
39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.952-10036C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842090 | |||||||
chr7:152842239 | A | G | 1 | a0001c0001t0002g0037 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.952-9887A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842239 | |||||||
chr7:152842286 | G | A | 11 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(8): Show |
11 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.952-9840G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842286 | |||||||
chr7:152842521 | G | T | 12 | a0001c0001t0001g0182 a0001c0001t0003g0168 a0001c0001t0003g0170 others(9): Show |
12 | HG01891.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.952-9605G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842521 | |||||||
chr7:152842564 | C | T | 16 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(13): Show |
16 | HG01074.hp2 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-9562C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842564 | |||||||
chr7:152842572 | C | CT | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.952-9553dupT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152842572 | ||||||
chr7:152842579 | C | T | 16 | a0001c0001t0002g0009 a0001c0001t0002g0157 a0001c0001t0002g0158 others(13): Show |
16 | HG01074.hp2 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-9547C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842579 | |||||||
chr7:152842755 | G | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-9371G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842755 | |||||||
chr7:152842856 | T | C | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-9270T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842856 | |||||||
chr7:152842863 | A | G | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.952-9263A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842863 | |||||||
chr7:152842869 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.952-9257G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152842869 | |||||||
chr7:152843034 | C | T | 250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.952-9092C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843034 | |||||||
chr7:152843154 | A | T | 37 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(34): Show |
38 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.952-8972A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843154 | |||||||
chr7:152843229 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.952-8897T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843229 | |||||||
chr7:152843290 | T | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0183 a0001c0001t0001g0196 others(113): Show |
117 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.952-8836T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843290 | |||||||
chr7:152843392 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.952-8734C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843392 | |||||||
chr7:152843485 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.952-8641C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843485 | |||||||
chr7:152843534 | G | T | 22 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(19): Show |
22 | HG00423.hp2 HG00558.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.952-8592G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843534 | |||||||
chr7:152843827 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-8299C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843827 | |||||||
chr7:152843914 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.952-8212C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843914 | |||||||
chr7:152843933 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.952-8193A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152843933 | |||||||
chr7:152844045 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(35): Show |
39 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.952-8081A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844045 | |||||||
chr7:152844160 | C | A | 2 | a0001c0001t0005g0261 a0001c0001t0008g0305 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.952-7966C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844160 | |||||||
chr7:152844171 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-7955C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844171 | |||||||
chr7:152844205 | A | G | 251 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(252): Show |
intron_variant | MODIFIER | c.952-7921A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844205 | |||||||
chr7:152844340 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7786G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844340 | |||||||
chr7:152844344 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | NA18989.hp2 NA19002.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.952-7782C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844344 | |||||||
chr7:152844345 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7781G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844345 | |||||||
chr7:152844349 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.952-7777C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844349 | |||||||
chr7:152844465 | A | T | 2 | a0001c0001t0001g0298 a0001c0001t0002g0105 |
2 | HG01070.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.952-7661A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844465 | |||||||
chr7:152844569 | T | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0161 others(2): Show |
5 | HG01070.hp2 HG03209.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.952-7557T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844569 | |||||||
chr7:152844586 | C | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0161 others(3): Show |
6 | HG01070.hp2 HG03209.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-7540C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844586 | |||||||
chr7:152844606 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0161 others(5): Show |
8 | HG01070.hp2 HG03209.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.952-7520G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844606 | |||||||
chr7:152844644 | T | G | 15 | a0001c0001t0001g0183 a0001c0001t0002g0025 a0001c0001t0002g0026 others(12): Show |
15 | HG00099.hp1 HG00738.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.952-7482T>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844644 | |||||||
chr7:152844668 | C | A | 19 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0272 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-7458C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844668 | |||||||
chr7:152844690 | T | C | 7 | a0001c0001t0002g0046 a0001c0001t0002g0051 a0001c0001t0002g0058 others(4): Show |
7 | HG00438.hp1 HG02071.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-7436T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844690 | |||||||
chr7:152844710 | C | G | 3 | a0001c0001t0001g0300 a0001c0001t0002g0028 a0001c0004t0001g0301 |
3 | HG02257.hp1 HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.952-7416C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844710 | |||||||
chr7:152844752 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0183 a0001c0001t0001g0184 others(112): Show |
118 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.952-7374C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844752 | |||||||
chr7:152844789 | G | A | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0114 others(181): Show |
188 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.952-7337G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844789 | |||||||
chr7:152844811 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(165): Show |
170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.952-7315T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844811 | |||||||
chr7:152844892 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(126): Show |
131 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.952-7234A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844892 | |||||||
chr7:152844984 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0161 |
2 | HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.952-7142G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844984 | |||||||
chr7:152844997 | G | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-7129G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152844997 | |||||||
chr7:152845013 | C | T | 28 | a0001c0001t0001g0016 a0001c0001t0001g0112 a0001c0001t0001g0119 others(25): Show |
29 | HG00642.hp1 HG01106.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.952-7113C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845013 | |||||||
chr7:152845102 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0262 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.952-7024T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845102 | |||||||
chr7:152845113 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.952-7013G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845113 | |||||||
chr7:152845190 | GTAATA | G | 25 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0186 others(22): Show |
26 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.952-6928_952-6924d others(7): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152845190 | ||||||
chr7:152845204 | G | A | 17 | a0001c0001t0001g0149 a0001c0001t0001g0186 a0001c0001t0001g0188 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.952-6922G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845204 | |||||||
chr7:152845239 | G | T | 7 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0031 others(4): Show |
7 | HG02055.hp1 HG02615.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-6887G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845239 | |||||||
chr7:152845271 | T | C | 3 | a0001c0001t0004g0171 a0001c0001t0004g0172 a0001c0001t0004g0176 |
3 | HG01891.hp1 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952-6855T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845271 | |||||||
chr7:152845276 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.952-6850C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845276 | |||||||
chr7:152845296 | A | C | 14 | a0001c0001t0001g0149 a0001c0001t0001g0210 a0001c0001t0001g0224 others(11): Show |
15 | HG00423.hp1 HG01884.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.952-6830A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845296 | |||||||
chr7:152845374 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(3): Show |
6 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.952-6752G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845374 | |||||||
chr7:152845426 | GT | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0002g0021 |
3 | HG02818.hp1 HG06807.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.952-6695delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152845426 | ||||||
chr7:152845482 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.952-6644C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845482 | |||||||
chr7:152845531 | C | T | 19 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(16): Show |
19 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.952-6595C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845531 | |||||||
chr7:152845588 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.952-6538C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845588 | |||||||
chr7:152845598 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0069 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.952-6528T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845598 | |||||||
chr7:152845603 | C | G | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-6523C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845603 | |||||||
chr7:152845717 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-6409G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152845717 | |||||||
chr7:152846124 | CAGTCTGC others(24): Show |
C | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.952-5964_952-5934d others(33): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846124 | ||||||
chr7:152846207 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.952-5919G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846207 | |||||||
chr7:152846210 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.952-5916C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846210 | |||||||
chr7:152846245 | G | A | 2 | a0001c0001t0002g0160 a0001c0001t0002g0165 |
2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.952-5881G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846245 | |||||||
chr7:152846269 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5857C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846269 | |||||||
chr7:152846274 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5852G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846274 | |||||||
chr7:152846304 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.952-5822T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846304 | |||||||
chr7:152846335 | C | T | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952-5791C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846335 | |||||||
chr7:152846460 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.952-5666C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846460 | |||||||
chr7:152846555 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-5571G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846555 | |||||||
chr7:152846597 | C | CAGTGAGC others(55): Show |
20 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-5521_952-5460d others(64): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846597 | ||||||
chr7:152846597 | CAGTGAGC others(24): Show |
C | 2 | a0001c0001t0002g0070 a0001c0001t0002g0101 |
2 | HG01515.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.952-5490_952-5460d others(33): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846597 | ||||||
chr7:152846620 | GCA | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0286 a0001c0001t0001g0289 others(3): Show |
7 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-5505_952-5504d others(4): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846620 | |||||||
chr7:152846641 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0002g0009 a0001c0001t0002g0057 |
3 | HG00735.hp2 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952-5485C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846641 | |||||||
chr7:152846770 | C | T | 1 | a0001c0001t0004g0171 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.952-5356C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846770 | |||||||
chr7:152846785 | T | TAGTGAGC others(55): Show |
1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-5317_952-5256d others(64): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152846785 | ||||||
chr7:152846796 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.952-5330A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846796 | |||||||
chr7:152846895 | C | T | 6 | a0001c0001t0001g0244 a0001c0001t0001g0300 a0001c0001t0002g0002 others(3): Show |
7 | HG02630.hp2 HG03239.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.952-5231C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846895 | |||||||
chr7:152846927 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.952-5199G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846927 | |||||||
chr7:152846971 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(118): Show |
123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.952-5155C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846971 | |||||||
chr7:152846975 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.952-5151G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846975 | |||||||
chr7:152846988 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.952-5138C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846988 | |||||||
chr7:152846999 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.952-5127C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152846999 | |||||||
chr7:152847001 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-5125G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847001 | |||||||
chr7:152847062 | T | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(118): Show |
123 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.952-5064T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847062 | |||||||
chr7:152847083 | G | A | 2 | a0001c0001t0002g0028 a0001c0001t0002g0067 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.952-5043G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847083 | |||||||
chr7:152847113 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.952-5013G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847113 | |||||||
chr7:152847200 | A | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-4926A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847200 | |||||||
chr7:152847203 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.952-4923G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847203 | |||||||
chr7:152847256 | G | T | 5 | a0001c0001t0001g0182 a0001c0001t0002g0009 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-4870G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847256 | |||||||
chr7:152847436 | A | G | 2 | a0001c0001t0002g0158 a0001c0001t0002g0167 |
2 | HG01074.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.952-4690A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847436 | |||||||
chr7:152847552 | T | C | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(238): Show |
245 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.952-4574T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847552 | |||||||
chr7:152847610 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.952-4516G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847610 | |||||||
chr7:152847654 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-4472G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847654 | |||||||
chr7:152847696 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-4430G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847696 | |||||||
chr7:152847873 | C | A | 2 | a0001c0001t0001g0222 a0001c0001t0002g0091 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.952-4253C>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847873 | |||||||
chr7:152847898 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-4228G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847898 | |||||||
chr7:152847913 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.952-4213G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847913 | |||||||
chr7:152847939 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.952-4187G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847939 | |||||||
chr7:152847952 | A | T | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.952-4174A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847952 | |||||||
chr7:152847992 | A | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0067 others(1): Show |
4 | HG02280.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-4134A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152847992 | |||||||
chr7:152848085 | G | GAAT | 4 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-4038_952-4036d others(5): Show |
ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152848085 | ||||||
chr7:152848105 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-4021G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848105 | |||||||
chr7:152848266 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(121): Show |
126 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.952-3860G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848266 | |||||||
chr7:152848511 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.952-3615A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848511 | |||||||
chr7:152848521 | A | G | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.952-3605A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848521 | |||||||
chr7:152848614 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-3512G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848614 | |||||||
chr7:152848838 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-3288C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848838 | |||||||
chr7:152848957 | G | C | 20 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-3169G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152848957 | |||||||
chr7:152849049 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-3077G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849049 | |||||||
chr7:152849140 | A | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0067 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.952-2986A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849140 | |||||||
chr7:152849202 | A | G | 20 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-2924A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849202 | |||||||
chr7:152849237 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.952-2889C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849237 | |||||||
chr7:152849329 | T | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-2797T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849329 | |||||||
chr7:152849555 | G | T | 5 | a0001c0001t0001g0182 a0001c0001t0002g0009 a0001c0001t0002g0158 others(2): Show |
5 | HG01074.hp2 HG01099.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-2571G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849555 | |||||||
chr7:152849565 | G | A | 2 | a0001c0001t0002g0029 a0001c0001t0002g0099 |
2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.952-2561G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849565 | |||||||
chr7:152849670 | A | T | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-2456A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849670 | |||||||
chr7:152849674 | G | A | 1 | a0001c0005t0001g0299 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.952-2452G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849674 | |||||||
chr7:152849717 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.952-2409A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849717 | |||||||
chr7:152849723 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.952-2403T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849723 | |||||||
chr7:152849799 | A | C | 9 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0021 others(6): Show |
10 | HG01361.hp2 HG01884.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.952-2327A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849799 | |||||||
chr7:152849920 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(123): Show |
128 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.952-2206T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152849920 | |||||||
chr7:152850023 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-2103G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850023 | |||||||
chr7:152850190 | C | T | 5 | a0001c0001t0001g0190 a0001c0001t0001g0220 a0001c0001t0001g0221 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-1936C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850190 | |||||||
chr7:152850260 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.952-1866G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850260 | |||||||
chr7:152850354 | G | A | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.952-1772G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850354 | |||||||
chr7:152850490 | G | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(122): Show |
127 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.952-1636G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850490 | |||||||
chr7:152850513 | A | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-1613A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850513 | |||||||
chr7:152850557 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-1569G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850557 | |||||||
chr7:152850713 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.952-1413C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850713 | |||||||
chr7:152850763 | AT | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(17): Show |
21 | HG01099.hp2 HG01106.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.952-1354delT | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 152850763 | ||||||
chr7:152850795 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.952-1331C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850795 | |||||||
chr7:152850835 | C | T | 20 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-1291C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152850835 | |||||||
chr7:152851285 | A | G | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-841A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851285 | |||||||
chr7:152851314 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-812G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851314 | |||||||
chr7:152851332 | C | T | 35 | a0001c0001t0001g0119 a0001c0001t0001g0181 a0001c0001t0001g0269 others(32): Show |
36 | HG01109.hp1 HG01192.hp1 HG01952.hp1 others(33): Show |
intron_variant | MODIFIER | c.952-794C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851332 | |||||||
chr7:152851362 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.952-764T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851362 | |||||||
chr7:152851406 | A | G | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-720A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851406 | |||||||
chr7:152851428 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.952-698G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851428 | |||||||
chr7:152851506 | C | T | 20 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.952-620C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851506 | |||||||
chr7:152851545 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0291 a0001c0001t0005g0288 |
3 | HG02809.hp2 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.952-581C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851545 | |||||||
chr7:152851555 | G | A | 15 | a0001c0001t0001g0181 a0001c0001t0001g0287 a0001c0001t0001g0291 others(12): Show |
16 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.952-571G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851555 | |||||||
chr7:152851647 | G | C | 1 | a0001c0002t0001g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.952-479G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851647 | |||||||
chr7:152851766 | C | G | 233 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(230): Show |
237 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.952-360C>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851766 | |||||||
chr7:152851839 | T | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.952-287T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851839 | |||||||
chr7:152851923 | C | T | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00735.hp1 HG01891.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.952-203C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152851923 | |||||||
chr7:152852022 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0131 others(119): Show |
124 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.952-104C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852022 | |||||||
chr7:152852084 | G | A | 2 | a0001c0001t0005g0261 a0001c0001t0008g0305 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.952-42G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852084 | |||||||
chr7:152852088 | G | T | 18 | a0001c0001t0001g0119 a0001c0001t0001g0269 a0001c0001t0001g0270 others(15): Show |
18 | HG01109.hp1 HG01192.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.952-38G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 9/11 | chr7 | 152852088 | |||||||
chr7:152852273 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0302 |
2 | HG01952.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1077+22G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852273 | |||||||
chr7:152852305 | C | T | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0302 others(1): Show |
4 | HG01952.hp1 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+54C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852305 | |||||||
chr7:152852328 | G | A | 15 | a0001c0001t0001g0181 a0001c0001t0001g0287 a0001c0001t0001g0291 others(12): Show |
16 | HG01952.hp1 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1077+77G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852328 | |||||||
chr7:152852347 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1077+96G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852347 | |||||||
chr7:152852407 | G | A | 5 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(2): Show |
5 | HG01952.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+156G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852407 | |||||||
chr7:152852464 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1077+213A>G | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852464 | |||||||
chr7:152852813 | A | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0007 |
2 | NA18939.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1077+562A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852813 | |||||||
chr7:152852831 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1077+580G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852831 | |||||||
chr7:152852948 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1078-546A>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152852948 | |||||||
chr7:152853054 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1078-440G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853054 | |||||||
chr7:152853059 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1078-435G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853059 | |||||||
chr7:152853077 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
42 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1078-417T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853077 | |||||||
chr7:152853134 | T | TA | 33 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(30): Show |
33 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1078-359dupA | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr7 | 152853134 | ||||||
chr7:152853146 | T | A | 4 | a0001c0001t0001g0294 a0001c0001t0002g0003 a0001c0001t0002g0179 others(1): Show |
5 | HG01884.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-348T>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853146 | |||||||
chr7:152853237 | G | A | 5 | a0001c0001t0001g0300 a0001c0001t0002g0002 a0001c0001t0002g0159 others(2): Show |
6 | HG02630.hp2 HG03490.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-257G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853237 | |||||||
chr7:152853262 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1078-232G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853262 | |||||||
chr7:152853295 | G | C | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1078-199G>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853295 | |||||||
chr7:152853359 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
42 | HG01099.hp2 HG01106.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1078-135T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853359 | |||||||
chr7:152853413 | C | T | 8 | a0001c0001t0003g0168 a0001c0001t0003g0170 a0001c0001t0003g0173 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1078-81C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853413 | |||||||
chr7:152853414 | T | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.1078-80T>C | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853414 | |||||||
chr7:152853458 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1078-36G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853458 | |||||||
chr7:152853464 | G | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0285 a0001c0001t0002g0072 |
3 | HG00099.hp1 HG01256.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1078-30G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 10/11 | chr7 | 152853464 | |||||||
chr7:152853608 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1161+31C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853608 | |||||||
chr7:152853780 | G | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0177 |
3 | HG01361.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1161+203G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853780 | |||||||
chr7:152853780 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1161+203G>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853780 | |||||||
chr7:152853834 | A | T | 1 | a0001c0004t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1161+257A>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853834 | |||||||
chr7:152853862 | G | A | 1 | a0002c0006t0001g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1161+285G>A | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152853862 | |||||||
chr7:152854231 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-227C>T | ACTR3B | ENSG00000133627.18 | transcript | ENST00000256001.13 | protein_coding | 11/11 | chr7 | 152854231 |