Item | Value |
---|---|
geneid | 4507 |
ensemblid | ENSG00000099810.21 |
hgncid | 7413 |
symbol | MTAP |
name | methylthioadenosine phosphorylase |
refseq_nuc | NM_002451.4 |
refseq_prot | NP_002442.2 |
ensembl_nuc | ENST00000644715.2 |
ensembl_prot | ENSP00000494373.1 |
mane_status | MANE Select |
chr | chr9 |
start | 21802636 |
end | 21867081 |
strand | + |
ver | v1.2 |
region | chr9:21802636-21867081 |
region5000 | chr9:21797636-21872081 |
regionname0 | MTAP_chr9_21802636_21867081 |
regionname5000 | MTAP_chr9_21797636_21872081 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 283 | 243 | 47 | 37 | 123 | 10 | 25 | 96 | MTAP_chr9_21797636_21872081 | MTAP | MASGT others(278): Show |
chr9 | 21797636 | 21872081 |
a0002 | 0/1 | 283 | 135 | 44 | 25 | 46 | 6 | 13 | 39 | MTAP_chr9_21797636_21872081 | MTAP | MASGT others(278): Show |
chr9 | 21797636 | 21872081 |
a0003 | 0/0 | 283 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | MASGT others(278): Show |
chr9 | 21797636 | 21872081 |
a0004 | 0/0 | 283 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | MASGT others(278): Show |
chr9 | 21797636 | 21872081 |
a0005 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | MASGT others(278): Show |
chr9 | 21797636 | 21872081 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 849 | 222 | 45 | 35 | 107 | 10 | 24 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0001c0003 | 0/0 | 849 | 16 | 0 | 1 | 14 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0001c0006 | 0/0 | 849 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0001c0007 | 0/0 | 849 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0001c0010 | 0/0 | 849 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0002c0002 | 0/1 | 849 | 129 | 44 | 22 | 46 | 4 | 12 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0002c0004 | 0/0 | 849 | 6 | 0 | 3 | 0 | 2 | 1 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0003c0005 | 0/0 | 849 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0004c0009 | 0/0 | 849 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 | ||
a0005c0008 | 0/0 | 849 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | ATGGC others(844): Show |
chr9 | 21797636 | 21872081 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 6032 | 84 | 14 | 18 | 32 | 7 | 12 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0002 | 0/0 | 6032 | 15 | 1 | 4 | 9 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0003 | 0/0 | 6031 | 45 | 9 | 4 | 25 | 1 | 6 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0004 | 0/0 | 6032 | 3 | 3 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0005 | 0/0 | 6031 | 14 | 0 | 0 | 14 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0006 | 0/0 | 6031 | 5 | 0 | 0 | 5 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0008 | 0/0 | 6030 | 4 | 4 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6025): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0009 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0010 | 0/0 | 6032 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0011 | 0/0 | 6032 | 2 | 0 | 1 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0012 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0014 | 0/0 | 6031 | 4 | 0 | 2 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0015 | 0/0 | 6031 | 4 | 0 | 4 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0017 | 0/0 | 6032 | 3 | 0 | 0 | 3 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0018 | 0/0 | 6032 | 3 | 0 | 1 | 0 | 1 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0019 | 0/0 | 6031 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0020 | 0/0 | 6032 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0021 | 0/0 | 6018 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6013): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0023 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0024 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0025 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0028 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0029 | 0/0 | 6031 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0030 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0031 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0034 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0035 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0040 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0041 | 0/0 | 6031 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0042 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0043 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0045 | 0/0 | 6031 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0046 | 0/0 | 6031 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0049 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0001t0050 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6025): Show |
chr9 | 21797636 | 21872081 |
a0001c0003t0001 | 0/0 | 6032 | 15 | 0 | 1 | 13 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0003t0003 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0006t0001 | 0/0 | 6032 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0001c0007t0003 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0001c0010t0009 | 0/0 | 6031 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0001 | 0/0 | 6032 | 16 | 2 | 2 | 10 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0002 | 0/0 | 6032 | 48 | 5 | 15 | 24 | 0 | 4 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0003 | 0/0 | 6031 | 10 | 2 | 1 | 3 | 0 | 4 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0004 | 0/0 | 6032 | 21 | 20 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0005 | 0/0 | 6031 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0007 | 0/0 | 6031 | 5 | 3 | 0 | 0 | 2 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0008 | 0/0 | 6030 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6025): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0011 | 0/0 | 6032 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0012 | 0/0 | 6031 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0013 | 0/0 | 6032 | 4 | 0 | 0 | 4 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0016 | 0/0 | 6032 | 3 | 2 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0022 | 0/0 | 6033 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6028): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0026 | 0/0 | 6033 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6028): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0027 | 0/1 | 6032 | 2 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0032 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0033 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0036 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0037 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0038 | 0/0 | 6032 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0039 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0044 | 0/0 | 6032 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0047 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0048 | 0/0 | 6030 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6025): Show |
chr9 | 21797636 | 21872081 |
a0002c0002t0051 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0002c0004t0001 | 0/0 | 6032 | 6 | 0 | 3 | 0 | 2 | 1 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0003c0005t0002 | 0/0 | 6032 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
a0004c0009t0009 | 0/0 | 6031 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6026): Show |
chr9 | 21797636 | 21872081 |
a0005c0008t0002 | 0/0 | 6032 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | CTCCG others(6027): Show |
chr9 | 21797636 | 21872081 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0017 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0010g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0011g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0011g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0014g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0015g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0017g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0017g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0018g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0018g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0019g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0020g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0020g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0021g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0021g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0023g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0023g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0024g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0025g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0028g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0028g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0029g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0030g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0031g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0034g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0035g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0040g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0041g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0042g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0043g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0045g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0046g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0049g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0001t0050g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0006t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0007t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0007t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0001c0010t0009g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0011g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0012g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0013g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0016g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0022g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0022g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0026g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0026g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0027g0317 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0027g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0032g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0033g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0036g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0037g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0038g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0039g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0044g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0047g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0048g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0002t0051g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0002c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0003c0005t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0004c0009t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
a0005c0008t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0018 | g0027 | EUR | GBR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | GBR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00280 | hp2 | a0002 | c0004 | t0001 | g0082 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0115 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0214 | EUR | FIN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00408 | hp1 | a0001 | c0001 | t0030 | g0248 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0204 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00544 | hp1 | a0002 | c0002 | t0003 | g0122 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00597 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00609 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0254 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0013 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | CHS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0200 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0012 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01074 | hp1 | a0002 | c0002 | t0016 | g0138 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01081 | hp1 | a0002 | c0004 | t0001 | g0111 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01081 | hp2 | a0001 | c0001 | t0014 | g0264 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01106 | hp1 | a0001 | c0001 | t0018 | g0276 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0107 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01167 | hp1 | a0002 | c0002 | t0022 | g0114 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01169 | hp2 | a0002 | c0002 | t0022 | g0113 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01192 | hp2 | a0002 | c0002 | t0004 | g0313 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01243 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | PUR | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0119 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0092 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01361 | hp1 | a0001 | c0001 | t0015 | g0005 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0284 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0041 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01516 | hp2 | a0002 | c0002 | t0007 | g0030 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01517 | hp1 | a0002 | c0002 | t0007 | g0038 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01884 | hp1 | a0002 | c0002 | t0008 | g0309 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01884 | hp2 | a0002 | c0002 | t0039 | g0294 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0311 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01934 | hp2 | a0001 | c0001 | t0015 | g0005 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0093 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0094 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01975 | hp2 | a0001 | c0001 | t0015 | g0181 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01978 | hp2 | a0002 | c0004 | t0001 | g0055 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01981 | hp1 | a0001 | c0001 | t0045 | g0277 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02004 | hp2 | a0001 | c0001 | t0014 | g0268 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02027 | hp1 | a0001 | c0001 | t0028 | g0194 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02055 | hp2 | a0001 | c0001 | t0023 | g0058 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02145 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0133 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02258 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02273 | hp2 | a0001 | c0001 | t0015 | g0164 | AMR | PEL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02280 | hp1 | a0002 | c0002 | t0004 | g0297 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02523 | hp2 | a0001 | c0003 | t0003 | g0048 | EAS | KHV | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02572 | hp2 | a0002 | c0002 | t0004 | g0067 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02602 | hp2 | a0001 | c0001 | t0040 | g0291 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02630 | hp1 | a0001 | c0001 | t0024 | g0197 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02630 | hp2 | a0002 | c0002 | t0016 | g0139 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0312 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0280 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02717 | hp1 | a0002 | c0002 | t0004 | g0298 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02717 | hp2 | a0002 | c0002 | t0016 | g0137 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02809 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0287 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0310 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02896 | hp1 | a0002 | c0002 | t0004 | g0296 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02896 | hp2 | a0002 | c0002 | t0051 | g0299 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0307 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02897 | hp2 | a0002 | c0002 | t0004 | g0295 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0199 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02970 | hp1 | a0001 | c0001 | t0021 | g0263 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02970 | hp2 | a0001 | c0007 | t0003 | g0136 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02976 | hp1 | a0002 | c0002 | t0004 | g0305 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0088 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03017 | hp2 | a0001 | c0001 | t0046 | g0159 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03041 | hp2 | a0002 | c0002 | t0033 | g0070 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03098 | hp2 | a0001 | c0001 | t0024 | g0190 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03130 | hp2 | a0002 | c0002 | t0004 | g0306 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03139 | hp1 | a0002 | c0002 | t0007 | g0303 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03139 | hp2 | a0002 | c0002 | t0004 | g0300 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03225 | hp2 | a0002 | c0002 | t0007 | g0301 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03239 | hp1 | a0002 | c0004 | t0001 | g0110 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03239 | hp2 | a0001 | c0001 | t0041 | g0040 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0066 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0314 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03490 | hp1 | a0002 | c0002 | t0011 | g0059 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03490 | hp2 | a0003 | c0005 | t0002 | g0009 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03492 | hp2 | a0003 | c0005 | t0002 | g0009 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03516 | hp1 | a0002 | c0002 | t0004 | g0308 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03516 | hp2 | a0001 | c0001 | t0023 | g0147 | AFR | ESN | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03540 | hp1 | a0001 | c0001 | t0012 | g0166 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03540 | hp2 | a0002 | c0002 | t0004 | g0073 | AFR | GWD | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03579 | hp1 | a0002 | c0002 | t0036 | g0069 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03579 | hp2 | a0002 | c0002 | t0044 | g0304 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0079 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03688 | hp1 | a0002 | c0002 | t0038 | g0001 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03704 | hp1 | a0002 | c0002 | t0003 | g0065 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03704 | hp2 | a0001 | c0001 | t0018 | g0027 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03710 | hp2 | a0001 | c0001 | t0043 | g0332 | SAS | PJL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0075 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03834 | hp1 | a0002 | c0002 | t0003 | g0081 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0045 | SAS | BEB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0128 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04199 | hp2 | a0002 | c0002 | t0011 | g0076 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04204 | hp2 | a0002 | c0002 | t0027 | g0330 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | STU | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18522 | hp1 | a0001 | c0001 | t0034 | g0182 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0257 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18747 | hp2 | a0001 | c0001 | t0028 | g0162 | EAS | CHB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18906 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18939 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18942 | hp2 | a0002 | c0002 | t0013 | g0112 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18947 | hp1 | a0001 | c0001 | t0019 | g0240 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0326 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18949 | hp2 | a0001 | c0001 | t0042 | g0172 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18951 | hp2 | a0002 | c0002 | t0026 | g0008 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18953 | hp1 | a0001 | c0001 | t0029 | g0018 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18957 | hp2 | a0002 | c0002 | t0013 | g0010 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18963 | hp1 | a0002 | c0002 | t0005 | g0071 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18968 | hp2 | a0001 | c0001 | t0029 | g0018 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18969 | hp1 | a0001 | c0001 | t0017 | g0021 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18974 | hp1 | a0002 | c0002 | t0048 | g0120 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18982 | hp1 | a0001 | c0001 | t0049 | g0032 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0087 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18986 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18987 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18990 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18994 | hp2 | a0001 | c0001 | t0006 | g0205 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18997 | hp1 | a0001 | c0001 | t0050 | g0170 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18997 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18999 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18999 | hp2 | a0001 | c0006 | t0001 | g0216 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19003 | hp1 | a0001 | c0001 | t0005 | g0244 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0206 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19006 | hp1 | a0001 | c0001 | t0017 | g0217 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19007 | hp1 | a0002 | c0002 | t0047 | g0011 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19009 | hp1 | a0001 | c0001 | t0017 | g0021 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0035 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19011 | hp1 | a0002 | c0002 | t0003 | g0086 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19043 | hp1 | a0002 | c0002 | t0032 | g0068 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19056 | hp2 | a0002 | c0002 | t0013 | g0121 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19057 | hp2 | a0001 | c0001 | t0014 | g0322 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19058 | hp1 | a0001 | c0001 | t0025 | g0033 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19060 | hp1 | a0001 | c0001 | t0019 | g0241 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19060 | hp2 | a0005 | c0008 | t0002 | g0123 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19070 | hp1 | a0001 | c0001 | t0014 | g0020 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19070 | hp2 | a0002 | c0002 | t0013 | g0010 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19074 | hp2 | a0001 | c0001 | t0035 | g0321 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19082 | hp1 | a0001 | c0001 | t0025 | g0033 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19085 | hp1 | a0002 | c0002 | t0026 | g0095 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19088 | hp1 | a0001 | c0006 | t0001 | g0218 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0318 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19240 | hp1 | a0002 | c0002 | t0003 | g0302 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA19240 | hp2 | a0001 | c0001 | t0031 | g0148 | AFR | YRI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ASW | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20129 | hp2 | a0001 | c0007 | t0003 | g0135 | AFR | ASW | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0012 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0077 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01123 | hp1 | a0001 | c0010 | t0009 | g0057 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0106 | AMR | CLM | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02109 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02109 | hp2 | a0002 | c0002 | t0012 | g0316 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02559 | hp1 | a0001 | c0001 | t0020 | g0149 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG02559 | hp2 | a0002 | c0002 | t0037 | g0089 | AFR | ACB | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03471 | hp1 | a0002 | c0002 | t0007 | g0030 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG06807 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
HG06807 | hp2 | a0004 | c0009 | t0009 | g0037 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0201 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | USA | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
NA21309 | hp2 | a0002 | c0002 | t0012 | g0315 | AFR | LWK | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
homoSapiens | chm13v2 | a0002 | c0002 | t0027 | g0317 | REF | REF | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0282 | REF | REF | MTAP_chr9_21797636_21872081 | MTAP | chr9 | 21797636 | 21872081 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21816759 | G | A | 2 | a0002 a0005 |
135 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(132): Show |
missense_variant | MODERATE | c.166G>A | p.Val56Ile | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/8 | 279/6032 | 166/852 | 56/283 | chr9 | 21816759 | |||
chr9:21818168 | G | A | 1 | a0003 | 2 | HG03490.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.313G>A | p.Gly105Ser | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 426/6032 | 313/852 | 105/283 | chr9 | 21818168 | |||
chr9:21854817 | G | A | 1 | a0004 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.637G>A | p.Ala213Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 750/6032 | 637/852 | 213/283 | chr9 | 21854817 | |||
chr9:21854826 | G | A | 1 | a0005 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.646G>A | p.Ala216Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 759/6032 | 646/852 | 216/283 | chr9 | 21854826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21818167 | C | T | 1 | a0001c0007 | 2 | HG02970.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.312C>T | p.Pro104Pro | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 425/6032 | 312/852 | 104/283 | chr9 | 21818167 | |||
chr9:21818170 | C | T | 1 | a0001c0006 | 2 | NA18999.hp2 NA19088.hp1 |
synonymous_variant | LOW | c.315C>T | p.Gly105Gly | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/8 | 428/6032 | 315/852 | 105/283 | chr9 | 21818170 | |||
chr9:21854741 | C | T | 2 | a0001c0003 a0002c0004 |
22 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(19): Show |
synonymous_variant | LOW | c.561C>T | p.Arg187Arg | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 674/6032 | 561/852 | 187/283 | chr9 | 21854741 | |||
chr9:21854774 | A | G | 2 | a0001c0010 a0004c0009 |
2 | HG01123.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.594A>G | p.Thr198Thr | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/8 | 707/6032 | 594/852 | 198/283 | chr9 | 21854774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21802646 | C | G | 1 | a0002c0002t0051 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-103C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/8 | 103 | chr9 | 21802646 | ||||||
chr9:21802702 | C | A | 1 | a0001c0001t0030 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/8 | 47 | chr9 | 21802702 | ||||||
chr9:21862119 | C | T | 1 | a0001c0001t0029 | 2 | NA18953.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 105 | chr9 | 21862119 | ||||||
chr9:21862272 | A | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(28): Show |
191 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*258A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 258 | chr9 | 21862272 | ||||||
chr9:21862273 | C | A | 13 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0019 others(10): Show |
31 | HG00597.hp1 HG00609.hp2 HG01074.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*259C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 259 | chr9 | 21862273 | ||||||
chr9:21862317 | G | T | 1 | a0001c0001t0002 | 2 | NA18951.hp1 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*303G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 303 | chr9 | 21862317 | ||||||
chr9:21862320 | G | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*306G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 306 | chr9 | 21862320 | ||||||
chr9:21862322 | G | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 308 | chr9 | 21862322 | ||||||
chr9:21862323 | G | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 309 | chr9 | 21862323 | ||||||
chr9:21862324 | G | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*310G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 310 | chr9 | 21862324 | ||||||
chr9:21862326 | A | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 312 | chr9 | 21862326 | ||||||
chr9:21862329 | C | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 315 | chr9 | 21862329 | ||||||
chr9:21862332 | T | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 318 | chr9 | 21862332 | ||||||
chr9:21862334 | C | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 320 | chr9 | 21862334 | ||||||
chr9:21862336 | T | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 322 | chr9 | 21862336 | ||||||
chr9:21862337 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 323 | chr9 | 21862337 | ||||||
chr9:21862338 | C | G | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 324 | chr9 | 21862338 | ||||||
chr9:21862342 | T | C | 2 | a0001c0001t0010 a0001c0001t0035 |
5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*328T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 328 | chr9 | 21862342 | ||||||
chr9:21862344 | C | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 330 | chr9 | 21862344 | ||||||
chr9:21862346 | G | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*332G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 332 | chr9 | 21862346 | ||||||
chr9:21862347 | C | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*333C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 333 | chr9 | 21862347 | ||||||
chr9:21862348 | C | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*334C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 334 | chr9 | 21862348 | ||||||
chr9:21862355 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 341 | chr9 | 21862355 | ||||||
chr9:21862356 | G | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 342 | chr9 | 21862356 | ||||||
chr9:21862358 | G | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 344 | chr9 | 21862358 | ||||||
chr9:21862360 | G | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*346G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 346 | chr9 | 21862360 | ||||||
chr9:21862361 | G | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*347G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 347 | chr9 | 21862361 | ||||||
chr9:21862364 | G | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*350G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 350 | chr9 | 21862364 | ||||||
chr9:21862367 | A | G | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*353A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 353 | chr9 | 21862367 | ||||||
chr9:21862381 | T | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*367T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 367 | chr9 | 21862381 | ||||||
chr9:21862382 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 368 | chr9 | 21862382 | ||||||
chr9:21862384 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 370 | chr9 | 21862384 | ||||||
chr9:21862385 | T | G | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 371 | chr9 | 21862385 | ||||||
chr9:21862386 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 372 | chr9 | 21862386 | ||||||
chr9:21862387 | A | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*373A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 373 | chr9 | 21862387 | ||||||
chr9:21862388 | T | G | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*374T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 374 | chr9 | 21862388 | ||||||
chr9:21862392 | T | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*378T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 378 | chr9 | 21862392 | ||||||
chr9:21862394 | C | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 380 | chr9 | 21862394 | ||||||
chr9:21862397 | C | A | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 383 | chr9 | 21862397 | ||||||
chr9:21862398 | T | C | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 384 | chr9 | 21862398 | ||||||
chr9:21862399 | G | T | 1 | a0001c0001t0041 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 385 | chr9 | 21862399 | ||||||
chr9:21862407 | G | C | 3 | a0001c0001t0005 a0001c0001t0019 a0002c0002t0005 |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*393G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 393 | chr9 | 21862407 | ||||||
chr9:21862550 | G | A | 2 | a0001c0001t0011 a0002c0002t0011 |
4 | HG00323.hp2 HG00639.hp2 HG03490.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*536G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 536 | chr9 | 21862550 | ||||||
chr9:21862671 | T | C | 2 | a0001c0001t0012 a0002c0002t0012 |
4 | HG02109.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*657T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 657 | chr9 | 21862671 | ||||||
chr9:21862782 | C | CA | 2 | a0001c0001t0004 a0002c0002t0004 |
24 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*775dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 776 | INFO_REALIGN_3_PRIME | chr9 | 21862782 | |||||
chr9:21862811 | C | T | 2 | a0001c0001t0004 a0002c0002t0004 |
24 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*797C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 797 | chr9 | 21862811 | ||||||
chr9:21862818 | T | C | 1 | a0002c0002t0016 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*804T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 804 | chr9 | 21862818 | ||||||
chr9:21862824 | TTGGGGGA others(7): Show |
T | 1 | a0001c0001t0021 | 2 | HG02647.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*815_*828delGGAGGG others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 815 | INFO_REALIGN_3_PRIME | chr9 | 21862824 | |||||
chr9:21862898 | T | A | 51 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(48): Show |
231 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*884T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 884 | chr9 | 21862898 | ||||||
chr9:21862916 | T | A | 1 | a0001c0001t0031 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*902T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 902 | chr9 | 21862916 | ||||||
chr9:21863052 | A | G | 1 | a0002c0002t0016 | 3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1038A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1038 | chr9 | 21863052 | ||||||
chr9:21863117 | AG | A | 2 | a0001c0001t0008 a0002c0002t0008 |
5 | HG01884.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1105delG | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1105 | INFO_REALIGN_3_PRIME | chr9 | 21863117 | |||||
chr9:21863195 | A | G | 1 | a0001c0001t0024 | 2 | HG02630.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1181A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1181 | chr9 | 21863195 | ||||||
chr9:21863537 | G | C | 1 | a0001c0001t0042 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1523G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1523 | chr9 | 21863537 | ||||||
chr9:21863622 | CA | C | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(32): Show |
198 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1622delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1622 | INFO_REALIGN_3_PRIME | chr9 | 21863622 | |||||
chr9:21863622 | CAA | C | 11 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0019 others(8): Show |
26 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1621_*1622delAA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1621 | INFO_REALIGN_3_PRIME | chr9 | 21863622 | |||||
chr9:21863657 | G | T | 3 | a0001c0001t0005 a0001c0001t0019 a0002c0002t0005 |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1643G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1643 | chr9 | 21863657 | ||||||
chr9:21863743 | G | A | 1 | a0002c0002t0013 | 4 | NA18942.hp2 NA18957.hp2 NA19056.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1729G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1729 | chr9 | 21863743 | ||||||
chr9:21863950 | C | T | 2 | a0001c0001t0015 a0001c0001t0029 |
6 | HG01361.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1936C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 1936 | chr9 | 21863950 | ||||||
chr9:21864071 | A | G | 1 | a0002c0002t0047 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2057A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2057 | chr9 | 21864071 | ||||||
chr9:21864099 | G | A | 32 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(29): Show |
120 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*2085G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2085 | chr9 | 21864099 | ||||||
chr9:21864202 | C | T | 1 | a0001c0001t0025 | 2 | NA19058.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2188C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2188 | chr9 | 21864202 | ||||||
chr9:21864269 | A | G | 5 | a0001c0001t0020 a0001c0001t0034 a0002c0002t0016 others(2): Show |
8 | HG01074.hp1 HG02559.hp1 HG02630.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2255A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2255 | chr9 | 21864269 | ||||||
chr9:21864350 | A | AT | 22 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(19): Show |
104 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2348dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2349 | INFO_REALIGN_3_PRIME | chr9 | 21864350 | |||||
chr9:21864379 | C | T | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
229 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2365C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2365 | chr9 | 21864379 | ||||||
chr9:21864536 | A | G | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0009 others(24): Show |
112 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*2522A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2522 | chr9 | 21864536 | ||||||
chr9:21864553 | A | G | 4 | a0001c0001t0012 a0001c0001t0023 a0002c0002t0012 others(1): Show |
7 | HG02055.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2539A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2539 | chr9 | 21864553 | ||||||
chr9:21864695 | A | G | 1 | a0001c0001t0031 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2681A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2681 | chr9 | 21864695 | ||||||
chr9:21864887 | C | T | 2 | a0001c0001t0020 a0001c0001t0034 |
3 | HG02559.hp1 HG02922.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2873C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 2873 | chr9 | 21864887 | ||||||
chr9:21865107 | T | C | 30 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(27): Show |
119 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3093T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3093 | chr9 | 21865107 | ||||||
chr9:21865154 | A | C | 1 | a0001c0001t0050 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3140A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3140 | chr9 | 21865154 | ||||||
chr9:21865158 | G | A | 1 | a0001c0001t0020 | 2 | HG02559.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3144G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3144 | chr9 | 21865158 | ||||||
chr9:21865321 | G | T | 1 | a0001c0001t0046 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3307G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3307 | chr9 | 21865321 | ||||||
chr9:21865375 | C | T | 1 | a0001c0001t0019 | 2 | NA18947.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3361C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3361 | chr9 | 21865375 | ||||||
chr9:21865385 | T | C | 1 | a0001c0001t0045 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3371T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3371 | chr9 | 21865385 | ||||||
chr9:21865843 | T | C | 52 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(49): Show |
232 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*3829T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3829 | chr9 | 21865843 | ||||||
chr9:21865865 | C | G | 2 | a0001c0001t0023 a0002c0002t0036 |
3 | HG02055.hp2 HG03516.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3851C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3851 | chr9 | 21865865 | ||||||
chr9:21865930 | C | T | 1 | a0001c0001t0018 | 3 | HG00140.hp1 HG01106.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3916C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3916 | chr9 | 21865930 | ||||||
chr9:21865960 | A | C | 27 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(24): Show |
102 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*3946A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3946 | chr9 | 21865960 | ||||||
chr9:21866013 | C | G | 1 | a0002c0002t0036 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3999C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 3999 | chr9 | 21866013 | ||||||
chr9:21866121 | A | C | 1 | a0001c0001t0035 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4107A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4107 | chr9 | 21866121 | ||||||
chr9:21866314 | C | G | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
192 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*4300C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4300 | chr9 | 21866314 | ||||||
chr9:21866501 | C | T | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
228 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*4487C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4487 | chr9 | 21866501 | ||||||
chr9:21866912 | G | C | 1 | a0002c0002t0027 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4898G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4898 | chr9 | 21866912 | ||||||
chr9:21866974 | A | G | 1 | a0001c0001t0017 | 3 | NA18969.hp1 NA19006.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4960A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 4960 | chr9 | 21866974 | ||||||
chr9:21867053 | T | C | 1 | a0002c0002t0007 | 5 | HG01516.hp2 HG01517.hp1 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5039T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 8/8 | 5039 | chr9 | 21867053 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:21802923 | C | G | 22 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0036 others(19): Show |
29 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.33+142C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802923 | |||||||
chr9:21802951 | G | A | 1 | a0004c0009t0009g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33+170G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802951 | |||||||
chr9:21802983 | C | CACACACA others(12): Show |
1 | a0002c0002t0007g0038 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.33+202_33+203insAC others(17): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802983 | |||||||
chr9:21802985 | A | AAC | 6 | a0001c0001t0012g0166 a0001c0010t0009g0057 a0002c0002t0002g0013 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+255_33+256dupAC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACAC | 7 | a0001c0001t0001g0026 a0001c0001t0002g0155 a0001c0001t0028g0162 others(4): Show |
7 | HG01516.hp1 HG01975.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.33+253_33+256dupAC others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACAC | 8 | a0001c0001t0001g0283 a0001c0003t0001g0046 a0001c0003t0003g0048 others(5): Show |
8 | HG00280.hp2 HG00621.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+251_33+256dupAC others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(1): Show |
10 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0242 others(7): Show |
10 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+249_33+256dupAC others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(3): Show |
13 | a0001c0001t0001g0243 a0001c0001t0001g0279 a0001c0001t0002g0290 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.33+247_33+256dupAC others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(5): Show |
14 | a0001c0001t0001g0025 a0001c0001t0001g0259 a0001c0001t0001g0324 others(11): Show |
14 | HG00323.hp1 HG01069.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+245_33+256dupAC others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(7): Show |
21 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0226 others(18): Show |
21 | HG00408.hp1 HG01099.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.33+243_33+256dupAC others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(9): Show |
23 | a0001c0001t0001g0026 a0001c0001t0001g0208 a0001c0001t0001g0232 others(20): Show |
24 | HG00673.hp1 HG00735.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.33+241_33+256dupAC others(14): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(11): Show |
14 | a0001c0001t0001g0022 a0001c0001t0001g0252 a0001c0001t0001g0274 others(11): Show |
14 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+239_33+256dupAC others(16): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(13): Show |
19 | a0001c0001t0001g0036 a0001c0001t0001g0210 a0001c0001t0001g0230 others(16): Show |
20 | HG01256.hp2 HG01981.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.33+237_33+256dupAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(15): Show |
10 | a0001c0001t0001g0231 a0001c0001t0001g0256 a0001c0001t0004g0131 others(7): Show |
10 | HG02027.hp2 HG02257.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+235_33+256dupAC others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(17): Show |
18 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0228 others(15): Show |
19 | HG01168.hp1 HG01433.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+233_33+256dupAC others(22): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(19): Show |
19 | a0001c0001t0001g0034 a0001c0001t0001g0227 a0001c0001t0001g0266 others(16): Show |
19 | HG00323.hp2 HG00738.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+231_33+256dupAC others(24): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(21): Show |
10 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0260 others(7): Show |
10 | HG00423.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+229_33+256dupAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(23): Show |
10 | a0001c0001t0001g0006 a0001c0001t0001g0262 a0001c0001t0005g0235 others(7): Show |
10 | HG01192.hp2 HG02896.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.33+227_33+256dupAC others(28): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(25): Show |
6 | a0001c0001t0001g0229 a0001c0001t0001g0271 a0001c0001t0005g0249 others(3): Show |
6 | HG00597.hp1 HG01496.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.33+225_33+256dupAC others(30): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(27): Show |
3 | a0001c0001t0001g0220 a0001c0001t0001g0270 a0002c0002t0004g0308 |
3 | HG01517.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.33+223_33+256dupAC others(32): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(29): Show |
1 | a0001c0001t0005g0236 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.33+221_33+256dupAC others(34): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(31): Show |
3 | a0001c0001t0001g0320 a0001c0003t0001g0049 a0001c0003t0001g0225 |
3 | NA18942.hp1 NA18948.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.33+219_33+256dupAC others(36): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(33): Show |
1 | a0001c0001t0005g0023 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.33+217_33+256dupAC others(38): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(39): Show |
1 | a0001c0001t0001g0215 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.33+211_33+256dupAC others(44): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | AACACACA others(102): Show |
1 | a0001c0001t0001g0219 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.33+256_33+257insAC others(107): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.33+204_33+205insCA others(9): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | A | ACACACAC others(12): Show |
1 | a0002c0002t0003g0302 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(17): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | A | ACACACAC others(16): Show |
2 | a0001c0001t0001g0211 a0002c0002t0008g0309 |
2 | HG01884.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.33+204_33+205insCA others(21): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | A | ACACACAC others(22): Show |
1 | a0001c0003t0001g0043 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(27): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | A | ACACACAC others(26): Show |
1 | a0001c0001t0005g0246 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.33+204_33+205insCA others(31): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | A | ACACACAC others(28): Show |
1 | a0001c0001t0021g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.33+204_33+205insCA others(33): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21802985 | |||||||
chr9:21802985 | AAC | A | 17 | a0001c0001t0003g0002 a0001c0001t0003g0175 a0001c0001t0034g0182 others(14): Show |
17 | HG00639.hp1 HG01071.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.33+255_33+256delAC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACAC | A | 25 | a0001c0001t0001g0193 a0001c0001t0002g0171 a0001c0001t0003g0002 others(22): Show |
26 | HG00544.hp1 HG00673.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.33+253_33+256delAC others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACAC | A | 24 | a0001c0001t0001g0158 a0001c0001t0002g0151 a0001c0001t0002g0207 others(21): Show |
26 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.33+251_33+256delAC others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(1): Show |
A | 19 | a0001c0001t0001g0198 a0001c0001t0002g0020 a0001c0001t0002g0156 others(16): Show |
19 | HG00438.hp1 HG02074.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.33+249_33+256delAC others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(3): Show |
A | 13 | a0001c0001t0001g0143 a0001c0001t0001g0251 a0001c0001t0003g0183 others(10): Show |
14 | HG02055.hp1 HG02129.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.33+247_33+256delAC others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(5): Show |
A | 7 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0174 others(4): Show |
8 | HG01891.hp2 HG02738.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.33+245_33+256delAC others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(7): Show |
A | 1 | a0002c0002t0002g0084 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.33+243_33+256delAC others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(9): Show |
A | 11 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0144 others(8): Show |
12 | HG01074.hp1 HG01109.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+241_33+256delAC others(14): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(11): Show |
A | 1 | a0001c0001t0003g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33+239_33+256delAC others(16): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(13): Show |
A | 5 | a0002c0002t0001g0100 a0002c0002t0001g0124 a0002c0002t0001g0125 others(2): Show |
5 | NA18940.hp1 NA18941.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.33+237_33+256delAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(15): Show |
A | 1 | a0001c0001t0001g0140 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.33+235_33+256delAC others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802985 | AACACACA others(21): Show |
A | 1 | a0002c0002t0003g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33+229_33+256delAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802985 | ||||||
chr9:21802988 | A | ACACACAC others(66): Show |
1 | a0001c0001t0041g0040 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.33+211_33+283dupAC others(71): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21802988 | ||||||
chr9:21803012 | A | G | 1 | a0002c0002t0002g0318 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.33+231A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803012 | |||||||
chr9:21803036 | A | ACACACAC others(21): Show |
1 | a0004c0009t0009g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.33+256_33+257insAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | ||||||
chr9:21803036 | A | ACACACAC others(19): Show |
1 | a0001c0001t0009g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33+256_33+257insAC others(24): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | ||||||
chr9:21803036 | A | ACACACAC others(13): Show |
1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33+256_33+257insAC others(18): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803036 | ||||||
chr9:21803040 | C | CACACACA others(21): Show |
1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.33+259_33+260insAC others(26): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803040 | |||||||
chr9:21803100 | T | TC | 13 | a0001c0003t0001g0004 a0001c0003t0001g0041 a0001c0003t0001g0042 others(10): Show |
15 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.33+320dupC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803100 | ||||||
chr9:21803166 | A | G | 26 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(23): Show |
31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.33+385A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803166 | |||||||
chr9:21803184 | G | C | 205 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(202): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+403G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803184 | |||||||
chr9:21803217 | T | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0053 a0002c0002t0002g0054 |
4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+436T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803217 | |||||||
chr9:21803512 | C | T | 8 | a0001c0001t0002g0020 a0001c0001t0002g0207 a0001c0001t0006g0202 others(5): Show |
8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+731C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803512 | |||||||
chr9:21803560 | G | A | 1 | a0002c0004t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.33+779G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803560 | |||||||
chr9:21803628 | C | T | 1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.33+847C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803628 | |||||||
chr9:21803730 | T | TCTTAA | 205 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(202): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+952_33+953insAA others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21803730 | ||||||
chr9:21803760 | A | G | 1 | a0002c0002t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.33+979A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803760 | |||||||
chr9:21803859 | A | T | 67 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(64): Show |
76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.33+1078A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803859 | |||||||
chr9:21803878 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.33+1097T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803878 | |||||||
chr9:21803881 | C | A | 205 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(202): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+1100C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803881 | |||||||
chr9:21803898 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+1117A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803898 | |||||||
chr9:21803949 | T | C | 2 | a0002c0002t0002g0008 a0002c0002t0026g0008 |
2 | NA18951.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.33+1168T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21803949 | |||||||
chr9:21804522 | C | T | 1 | a0001c0001t0020g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33+1741C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804522 | |||||||
chr9:21804578 | T | C | 1 | a0002c0002t0002g0056 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.33+1797T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804578 | |||||||
chr9:21804618 | A | G | 205 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(202): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+1837A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804618 | |||||||
chr9:21804694 | A | G | 205 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(202): Show |
231 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.33+1913A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804694 | |||||||
chr9:21804704 | CAA | C | 67 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(64): Show |
76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.33+1925_33+1926del others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21804704 | ||||||
chr9:21804751 | A | G | 1 | a0001c0003t0001g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.33+1970A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804751 | |||||||
chr9:21804821 | C | T | 1 | a0001c0001t0023g0147 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.33+2040C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804821 | |||||||
chr9:21804877 | T | C | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0001t0031g0148 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+2096T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804877 | |||||||
chr9:21804887 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.33+2106G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21804887 | |||||||
chr9:21805064 | G | A | 1 | a0001c0001t0001g0006 | 3 | NA18980.hp1 NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.33+2283G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805064 | |||||||
chr9:21805209 | C | CAG | 204 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(201): Show |
230 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.33+2428_33+2429ins others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805209 | |||||||
chr9:21805304 | C | T | 1 | a0001c0001t0003g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.33+2523C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805304 | |||||||
chr9:21805924 | A | T | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.33+3143A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805924 | |||||||
chr9:21805925 | T | G | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.33+3144T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805925 | |||||||
chr9:21805934 | G | C | 1 | a0001c0001t0020g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.33+3153G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805934 | |||||||
chr9:21805990 | A | G | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+3209A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21805990 | |||||||
chr9:21806254 | T | C | 1 | a0001c0003t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.33+3473T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806254 | |||||||
chr9:21806296 | T | C | 3 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 |
3 | HG01123.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.33+3515T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806296 | |||||||
chr9:21806330 | G | T | 1 | a0001c0001t0001g0292 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.33+3549G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806330 | |||||||
chr9:21806331 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.33+3550A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806331 | |||||||
chr9:21806422 | A | G | 2 | a0001c0001t0002g0290 a0001c0001t0040g0291 |
2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.33+3641A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806422 | |||||||
chr9:21806456 | C | G | 1 | a0001c0001t0020g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33+3675C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806456 | |||||||
chr9:21806565 | G | A | 91 | a0001c0001t0003g0063 a0002c0002t0001g0074 a0002c0002t0001g0077 others(88): Show |
102 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.33+3784G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806565 | |||||||
chr9:21806918 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.33+4137C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806918 | |||||||
chr9:21806970 | C | A | 90 | a0001c0001t0003g0063 a0002c0002t0001g0074 a0002c0002t0001g0077 others(87): Show |
101 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.33+4189C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21806970 | |||||||
chr9:21807073 | C | T | 1 | a0002c0002t0002g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.33+4292C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807073 | |||||||
chr9:21807213 | A | G | 3 | a0002c0002t0001g0125 a0002c0002t0001g0126 a0002c0002t0001g0127 |
3 | NA18941.hp1 NA18989.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.33+4432A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807213 | |||||||
chr9:21807321 | A | G | 1 | a0002c0002t0001g0124 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.33+4540A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807321 | |||||||
chr9:21807328 | G | A | 11 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0215 others(8): Show |
12 | HG00323.hp2 HG01099.hp1 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+4547G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807328 | |||||||
chr9:21807358 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | NA18947.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.33+4577G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807358 | |||||||
chr9:21807518 | A | T | 2 | a0001c0001t0001g0288 a0001c0001t0001g0289 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.33+4737A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807518 | |||||||
chr9:21807574 | C | T | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+4793C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807574 | |||||||
chr9:21807659 | T | C | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+4878T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807659 | |||||||
chr9:21807736 | G | T | 1 | a0005c0008t0002g0123 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33+4955G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807736 | |||||||
chr9:21807835 | C | T | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33+5054C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807835 | |||||||
chr9:21807995 | A | G | 106 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(103): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.33+5214A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21807995 | |||||||
chr9:21808011 | C | G | 8 | a0001c0001t0002g0020 a0001c0001t0002g0207 a0001c0001t0006g0202 others(5): Show |
8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.33+5230C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808011 | |||||||
chr9:21808024 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.33+5243A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808024 | |||||||
chr9:21808061 | A | C | 1 | a0002c0002t0003g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.33+5280A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808061 | |||||||
chr9:21808209 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33+5428T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808209 | |||||||
chr9:21808265 | A | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.33+5484A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808265 | |||||||
chr9:21808306 | C | T | 3 | a0002c0002t0012g0315 a0002c0002t0012g0316 a0002c0002t0039g0294 |
3 | HG01884.hp2 HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33+5525C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808306 | |||||||
chr9:21808353 | G | A | 1 | a0002c0002t0011g0059 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.33+5572G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808353 | |||||||
chr9:21808410 | C | G | 107 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(104): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.33+5629C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808410 | |||||||
chr9:21808421 | C | CA | 12 | a0001c0003t0001g0004 a0001c0003t0001g0041 a0001c0003t0001g0042 others(9): Show |
14 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.33+5652dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | ||||||
chr9:21808421 | CA | C | 93 | a0001c0001t0003g0063 a0001c0001t0004g0131 a0001c0001t0012g0130 others(90): Show |
103 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.33+5652delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | ||||||
chr9:21808421 | CAAA | C | 104 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(101): Show |
119 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.33+5650_33+5652del others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21808421 | ||||||
chr9:21808467 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.33+5686T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808467 | |||||||
chr9:21808546 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.33+5765A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808546 | |||||||
chr9:21808571 | G | A | 3 | a0001c0001t0003g0016 a0001c0007t0003g0135 a0001c0007t0003g0136 |
4 | HG01433.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.33+5790G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808571 | |||||||
chr9:21808605 | A | C | 1 | a0001c0001t0002g0285 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.33+5824A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808605 | |||||||
chr9:21808606 | AC | A | 189 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(186): Show |
214 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.33+5826delC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808606 | |||||||
chr9:21808607 | C | A | 13 | a0001c0001t0001g0193 a0001c0001t0003g0192 a0001c0001t0003g0195 others(10): Show |
13 | HG00621.hp2 HG01192.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.33+5826C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808607 | |||||||
chr9:21808753 | T | G | 95 | a0001c0001t0003g0063 a0002c0002t0001g0074 a0002c0002t0001g0077 others(92): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.33+5972T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808753 | |||||||
chr9:21808777 | C | T | 1 | a0001c0001t0040g0291 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.33+5996C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808777 | |||||||
chr9:21808779 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0043g0332 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.33+5998C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808779 | |||||||
chr9:21808914 | C | T | 93 | a0001c0001t0003g0063 a0002c0002t0001g0074 a0002c0002t0001g0077 others(90): Show |
103 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.33+6133C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21808914 | |||||||
chr9:21809078 | T | A | 90 | a0001c0001t0003g0063 a0002c0002t0001g0074 a0002c0002t0001g0077 others(87): Show |
100 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.33+6297T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809078 | |||||||
chr9:21809334 | C | T | 105 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(102): Show |
120 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.34-6099C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809334 | |||||||
chr9:21809361 | C | T | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34-6072C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809361 | |||||||
chr9:21809362 | G | A | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-6071G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809362 | |||||||
chr9:21809393 | A | C | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-6040A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809393 | |||||||
chr9:21809595 | C | G | 1 | a0001c0003t0001g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.34-5838C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809595 | |||||||
chr9:21809638 | C | CA | 112 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(109): Show |
127 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.34-5781dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21809638 | ||||||
chr9:21809653 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.34-5780G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809653 | |||||||
chr9:21809803 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.34-5630G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809803 | |||||||
chr9:21809838 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.34-5595G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809838 | |||||||
chr9:21809858 | C | T | 12 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.34-5575C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809858 | |||||||
chr9:21809993 | A | C | 24 | a0001c0001t0009g0201 a0002c0002t0003g0302 a0002c0002t0003g0314 others(21): Show |
29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.34-5440A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21809993 | |||||||
chr9:21810231 | A | G | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-5202A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810231 | |||||||
chr9:21810272 | G | A | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.34-5161G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810272 | |||||||
chr9:21810307 | C | T | 16 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(13): Show |
21 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.34-5126C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810307 | |||||||
chr9:21810308 | A | G | 1 | a0001c0001t0015g0181 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.34-5125A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810308 | |||||||
chr9:21810412 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.34-5021A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810412 | |||||||
chr9:21810431 | A | AAGAG | 115 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(112): Show |
130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.34-5000_34-4997dup others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21810431 | ||||||
chr9:21810532 | T | G | 115 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(112): Show |
130 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.34-4901T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810532 | |||||||
chr9:21810703 | T | C | 1 | a0002c0002t0003g0065 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.34-4730T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810703 | |||||||
chr9:21810861 | G | C | 30 | a0001c0001t0001g0022 a0001c0001t0001g0224 a0001c0001t0001g0226 others(27): Show |
33 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.34-4572G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21810861 | |||||||
chr9:21811023 | CA | C | 8 | a0002c0002t0004g0003 a0002c0002t0004g0306 a0002c0002t0004g0307 others(5): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.34-4406delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21811023 | ||||||
chr9:21811028 | T | C | 110 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(107): Show |
125 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.34-4405T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811028 | |||||||
chr9:21811139 | C | G | 1 | a0002c0002t0002g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.34-4294C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811139 | |||||||
chr9:21811155 | A | G | 99 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0283 others(96): Show |
111 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.34-4278A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811155 | |||||||
chr9:21811250 | A | G | 13 | a0001c0003t0001g0004 a0001c0003t0001g0041 a0001c0003t0001g0042 others(10): Show |
15 | HG01496.hp2 HG02523.hp2 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.34-4183A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811250 | |||||||
chr9:21811274 | T | C | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.34-4159T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811274 | |||||||
chr9:21811442 | A | G | 110 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(107): Show |
125 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.34-3991A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811442 | |||||||
chr9:21811450 | A | AT | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
10 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-3973dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21811450 | ||||||
chr9:21811451 | T | A | 3 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 |
3 | HG01123.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.34-3982T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811451 | |||||||
chr9:21811534 | C | G | 111 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(108): Show |
126 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.34-3899C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811534 | |||||||
chr9:21811566 | G | A | 27 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 others(24): Show |
32 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.34-3867G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811566 | |||||||
chr9:21811785 | G | A | 3 | a0002c0002t0032g0068 a0002c0002t0033g0070 a0002c0002t0036g0069 |
3 | HG03041.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.34-3648G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811785 | |||||||
chr9:21811921 | T | C | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-3512T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21811921 | |||||||
chr9:21812025 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.34-3408T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812025 | |||||||
chr9:21812317 | G | A | 94 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(91): Show |
108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.34-3116G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812317 | |||||||
chr9:21812350 | T | A | 94 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(91): Show |
108 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.34-3083T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812350 | |||||||
chr9:21812553 | C | T | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.34-2880C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812553 | |||||||
chr9:21812721 | C | T | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(6): Show |
10 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.34-2712C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812721 | |||||||
chr9:21812770 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.34-2663T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812770 | |||||||
chr9:21812935 | C | T | 1 | a0001c0003t0001g0050 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.34-2498C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21812935 | |||||||
chr9:21813224 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.34-2209G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813224 | |||||||
chr9:21813242 | T | C | 123 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(120): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.34-2191T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813242 | |||||||
chr9:21813304 | A | C | 124 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(121): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.34-2129A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813304 | |||||||
chr9:21813313 | G | T | 2 | a0001c0001t0005g0249 a0001c0001t0030g0248 |
2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.34-2120G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813313 | |||||||
chr9:21813375 | C | T | 2 | a0001c0001t0005g0249 a0001c0001t0030g0248 |
2 | HG00408.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.34-2058C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813375 | |||||||
chr9:21813496 | C | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(119): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.34-1937C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813496 | |||||||
chr9:21813519 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(120): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.34-1914C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813519 | |||||||
chr9:21813570 | C | G | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.34-1863C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813570 | |||||||
chr9:21813580 | C | G | 1 | a0001c0001t0003g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.34-1853C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813580 | |||||||
chr9:21813596 | A | G | 26 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(23): Show |
31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1837A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813596 | |||||||
chr9:21813719 | C | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(199): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.34-1714C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813719 | |||||||
chr9:21813766 | G | A | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.34-1667G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813766 | |||||||
chr9:21813770 | G | C | 26 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 others(23): Show |
31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1663G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813770 | |||||||
chr9:21813771 | G | T | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.34-1662G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813771 | |||||||
chr9:21813773 | T | C | 26 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 others(23): Show |
31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.34-1660T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813773 | |||||||
chr9:21813786 | G | C | 1 | a0001c0001t0034g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.34-1647G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813786 | |||||||
chr9:21813949 | A | G | 2 | a0002c0002t0002g0117 a0002c0002t0002g0118 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.34-1484A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813949 | |||||||
chr9:21813970 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.34-1463A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21813970 | |||||||
chr9:21814169 | CT | C | 3 | a0002c0002t0005g0071 a0002c0002t0013g0010 a0002c0002t0013g0121 |
4 | NA18957.hp2 NA18963.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-1262delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr9 | 21814169 | ||||||
chr9:21814207 | T | G | 1 | a0001c0001t0003g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.34-1226T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814207 | |||||||
chr9:21814419 | C | T | 1 | a0002c0002t0001g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.34-1014C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814419 | |||||||
chr9:21814516 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.34-917T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814516 | |||||||
chr9:21814621 | C | G | 1 | a0001c0001t0006g0206 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.34-812C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814621 | |||||||
chr9:21814760 | A | G | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34-673A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814760 | |||||||
chr9:21814979 | C | A | 1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34-454C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21814979 | |||||||
chr9:21815148 | C | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-285C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815148 | |||||||
chr9:21815167 | G | T | 68 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(65): Show |
77 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.34-266G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815167 | |||||||
chr9:21815288 | T | G | 4 | a0002c0002t0002g0011 a0002c0002t0002g0072 a0002c0002t0047g0011 others(1): Show |
4 | NA18950.hp2 NA18974.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-145T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 1/7 | chr9 | 21815288 | |||||||
chr9:21815551 | T | C | 1 | a0002c0002t0012g0316 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.120+32T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815551 | |||||||
chr9:21815590 | T | TAA | 92 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(89): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.120+84_120+85dupAA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 21815590 | ||||||
chr9:21815590 | T | TAAA | 240 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(237): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.120+83_120+85dupAA others(1): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 21815590 | ||||||
chr9:21815749 | A | G | 2 | a0002c0004t0001g0110 a0002c0004t0001g0111 |
2 | HG01081.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.120+230A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815749 | |||||||
chr9:21815798 | C | T | 85 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(82): Show |
95 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.120+279C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815798 | |||||||
chr9:21815857 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.120+338A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815857 | |||||||
chr9:21815978 | G | A | 1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.120+459G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21815978 | |||||||
chr9:21816083 | A | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+564A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816083 | |||||||
chr9:21816154 | A | C | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.121-560A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816154 | |||||||
chr9:21816215 | C | G | 91 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(88): Show |
101 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.121-499C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816215 | |||||||
chr9:21816364 | T | G | 1 | a0002c0002t0002g0318 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.121-350T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816364 | |||||||
chr9:21816470 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.121-244A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816470 | |||||||
chr9:21816529 | A | G | 135 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(132): Show |
152 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.121-185A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816529 | |||||||
chr9:21816574 | G | A | 213 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(210): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.121-140G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816574 | |||||||
chr9:21816638 | T | C | 97 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0283 others(94): Show |
108 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.121-76T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816638 | |||||||
chr9:21816647 | A | G | 213 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(210): Show |
239 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.121-67A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 2/7 | chr9 | 21816647 | |||||||
chr9:21816800 | T | C | 1 | a0002c0002t0048g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.179+28T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21816800 | |||||||
chr9:21817088 | A | T | 1 | a0001c0001t0009g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.179+316A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817088 | |||||||
chr9:21817283 | A | C | 8 | a0001c0001t0002g0020 a0001c0001t0002g0207 a0001c0001t0006g0202 others(5): Show |
8 | HG00408.hp2 HG02083.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.179+511A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817283 | |||||||
chr9:21817286 | G | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+514G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817286 | |||||||
chr9:21817326 | G | A | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+554G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817326 | |||||||
chr9:21817327 | C | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.179+555C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817327 | |||||||
chr9:21817476 | A | G | 2 | a0002c0002t0002g0064 a0002c0002t0002g0109 |
2 | HG01069.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.180-559A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817476 | |||||||
chr9:21817525 | G | C | 15 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(12): Show |
20 | HG01516.hp2 HG01517.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.180-510G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817525 | |||||||
chr9:21817755 | A | G | 228 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(225): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.180-280A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817755 | |||||||
chr9:21817778 | T | C | 332 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0025 others(329): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(372): Show |
intron_variant | MODIFIER | c.180-257T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21817778 | |||||||
chr9:21818012 | C | T | 24 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(21): Show |
29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.180-23C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 3/7 | chr9 | 21818012 | |||||||
chr9:21818311 | C | T | 212 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(209): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.347+109C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818311 | |||||||
chr9:21818317 | C | CT | 40 | a0001c0001t0001g0036 a0001c0001t0001g0211 a0001c0001t0001g0219 others(37): Show |
41 | HG00597.hp1 HG00642.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.347+142dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | ||||||
chr9:21818317 | CT | C | 137 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(134): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.347+142delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | ||||||
chr9:21818317 | CTT | C | 16 | a0002c0002t0003g0065 a0002c0002t0004g0003 a0002c0002t0004g0295 others(13): Show |
20 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.347+141_347+142del others(2): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | ||||||
chr9:21818317 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+131_347+142del others(12): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21818317 | ||||||
chr9:21818514 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347+312G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818514 | |||||||
chr9:21818570 | C | T | 1 | a0002c0002t0044g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.347+368C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818570 | |||||||
chr9:21818609 | G | A | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.347+407G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818609 | |||||||
chr9:21818618 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0014g0268 others(1): Show |
4 | HG00738.hp2 HG01515.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+416C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818618 | |||||||
chr9:21818622 | G | C | 1 | a0001c0001t0003g0154 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.347+420G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818622 | |||||||
chr9:21818675 | A | G | 96 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0283 others(93): Show |
107 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.347+473A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818675 | |||||||
chr9:21818729 | T | C | 5 | a0002c0002t0004g0295 a0002c0002t0004g0296 a0002c0002t0004g0297 others(2): Show |
5 | HG01192.hp2 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+527T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21818729 | |||||||
chr9:21819027 | T | G | 1 | a0001c0001t0050g0170 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.347+825T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819027 | |||||||
chr9:21819044 | A | G | 2 | a0001c0001t0005g0246 a0002c0002t0002g0146 |
2 | NA18987.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.347+842A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819044 | |||||||
chr9:21819053 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.347+851G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819053 | |||||||
chr9:21819062 | T | A | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347+860T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819062 | |||||||
chr9:21819094 | T | C | 52 | a0001c0001t0001g0022 a0001c0001t0001g0220 a0001c0001t0001g0224 others(49): Show |
57 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.347+892T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819094 | |||||||
chr9:21819117 | G | T | 1 | a0001c0001t0029g0018 | 2 | NA18953.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.347+915G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819117 | |||||||
chr9:21819137 | C | CT | 202 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(199): Show |
227 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.347+949dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21819137 | ||||||
chr9:21819140 | T | TC | 3 | a0001c0001t0003g0183 a0001c0001t0003g0188 a0001c0001t0003g0189 |
3 | HG02145.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.347+938_347+939ins others(1): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819140 | |||||||
chr9:21819141 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+939T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819141 | |||||||
chr9:21819152 | A | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0154 a0001c0001t0003g0169 |
4 | HG00544.hp2 NA18966.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+950A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819152 | |||||||
chr9:21819183 | C | G | 24 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(21): Show |
29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.347+981C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819183 | |||||||
chr9:21819191 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.347+989G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819191 | |||||||
chr9:21819263 | T | C | 1 | a0001c0001t0008g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.347+1061T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819263 | |||||||
chr9:21819543 | A | T | 1 | a0002c0002t0002g0318 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.347+1341A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819543 | |||||||
chr9:21819723 | T | G | 36 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(33): Show |
39 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.347+1521T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819723 | |||||||
chr9:21819900 | A | G | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.347+1698A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21819900 | |||||||
chr9:21820081 | A | G | 7 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0023g0058 others(4): Show |
7 | HG01123.hp1 HG02055.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+1879A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820081 | |||||||
chr9:21820092 | T | C | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.347+1890T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820092 | |||||||
chr9:21820170 | G | T | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.347+1968G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820170 | |||||||
chr9:21820182 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.347+1980A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820182 | |||||||
chr9:21820289 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.347+2087G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820289 | |||||||
chr9:21820371 | T | G | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+2169T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820371 | |||||||
chr9:21820382 | C | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+2180C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820382 | |||||||
chr9:21820419 | T | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+2217T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820419 | |||||||
chr9:21820500 | A | G | 1 | a0002c0002t0002g0108 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.347+2298A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820500 | |||||||
chr9:21820503 | T | G | 1 | a0001c0001t0001g0242 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.347+2301T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820503 | |||||||
chr9:21820717 | C | G | 1 | a0001c0001t0008g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.347+2515C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820717 | |||||||
chr9:21820728 | T | G | 1 | a0001c0001t0050g0170 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.347+2526T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820728 | |||||||
chr9:21820816 | A | C | 3 | a0002c0002t0002g0015 a0002c0002t0002g0119 a0002c0002t0004g0073 |
4 | HG01255.hp2 HG02622.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+2614A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820816 | |||||||
chr9:21820875 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+2673C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21820875 | |||||||
chr9:21821027 | T | G | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+2825T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821027 | |||||||
chr9:21821032 | C | T | 11 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+2830C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821032 | |||||||
chr9:21821278 | T | A | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+3076T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821278 | |||||||
chr9:21821282 | A | G | 127 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0265 others(124): Show |
144 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.347+3080A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821282 | |||||||
chr9:21821372 | A | G | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3170A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821372 | |||||||
chr9:21821388 | A | G | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+3186A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821388 | |||||||
chr9:21821509 | C | T | 24 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(21): Show |
29 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(26): Show |
intron_variant | MODIFIER | c.347+3307C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821509 | |||||||
chr9:21821515 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+3313G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821515 | |||||||
chr9:21821549 | G | A | 1 | a0001c0001t0009g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347+3347G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821549 | |||||||
chr9:21821591 | T | A | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3389T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821591 | |||||||
chr9:21821593 | G | T | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+3391G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821593 | |||||||
chr9:21821595 | T | C | 1 | a0002c0002t0007g0301 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.347+3393T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821595 | |||||||
chr9:21821649 | T | C | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.347+3447T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821649 | |||||||
chr9:21821669 | TTTATTGA others(4): Show |
T | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347+3468_347+3478d others(13): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821669 | |||||||
chr9:21821670 | T | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0141 others(104): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.347+3468T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821670 | |||||||
chr9:21821678 | T | C | 3 | a0002c0002t0001g0088 a0002c0002t0001g0105 a0002c0002t0037g0089 |
3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.347+3476T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821678 | |||||||
chr9:21821719 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.347+3517C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821719 | |||||||
chr9:21821728 | G | T | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+3526G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821728 | |||||||
chr9:21821765 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0043g0332 |
2 | HG02735.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.347+3563T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821765 | |||||||
chr9:21821786 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.347+3584A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821786 | |||||||
chr9:21821952 | A | G | 4 | a0001c0001t0005g0239 a0001c0001t0005g0245 a0001c0001t0019g0240 others(1): Show |
4 | HG02015.hp1 NA18947.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+3750A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21821952 | |||||||
chr9:21822003 | A | G | 3 | a0001c0001t0010g0035 a0001c0001t0010g0326 a0001c0001t0035g0321 |
4 | NA18948.hp1 NA18990.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+3801A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822003 | |||||||
chr9:21822079 | A | G | 1 | a0001c0001t0014g0264 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.347+3877A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822079 | |||||||
chr9:21822108 | G | T | 1 | a0001c0003t0001g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.347+3906G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822108 | |||||||
chr9:21822193 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347+3991G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822193 | |||||||
chr9:21822210 | C | A | 1 | a0001c0001t0002g0156 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.347+4008C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822210 | |||||||
chr9:21822223 | G | A | 1 | a0002c0002t0001g0074 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.347+4021G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822223 | |||||||
chr9:21822227 | G | A | 2 | a0002c0002t0004g0306 a0002c0002t0004g0311 |
2 | HG01891.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.347+4025G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822227 | |||||||
chr9:21822299 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.347+4097A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822299 | |||||||
chr9:21822418 | A | G | 30 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(27): Show |
33 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.347+4216A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822418 | |||||||
chr9:21822484 | G | A | 228 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(225): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.347+4282G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822484 | |||||||
chr9:21822536 | T | A | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+4334T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822536 | |||||||
chr9:21822616 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0247 |
2 | NA18955.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.347+4414G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822616 | |||||||
chr9:21822647 | C | T | 1 | a0002c0002t0026g0095 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.347+4445C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822647 | |||||||
chr9:21822753 | G | T | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+4551G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822753 | |||||||
chr9:21822779 | A | T | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.347+4577A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822779 | |||||||
chr9:21822793 | G | C | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+4591G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21822793 | |||||||
chr9:21823089 | C | T | 23 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(20): Show |
28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+4887C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823089 | |||||||
chr9:21823150 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.347+4948T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823150 | |||||||
chr9:21823224 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+5022C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823224 | |||||||
chr9:21823460 | T | C | 1 | a0001c0001t0005g0233 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.347+5258T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823460 | |||||||
chr9:21823669 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.347+5467A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823669 | |||||||
chr9:21823715 | T | C | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+5513T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823715 | |||||||
chr9:21823742 | G | A | 1 | a0001c0001t0006g0206 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.347+5540G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823742 | |||||||
chr9:21823745 | AC | A | 3 | a0002c0002t0016g0137 a0002c0002t0016g0138 a0002c0002t0016g0139 |
3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.347+5544delC | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823745 | |||||||
chr9:21823756 | A | T | 1 | a0001c0001t0003g0195 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.347+5554A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823756 | |||||||
chr9:21823803 | G | A | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+5601G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823803 | |||||||
chr9:21823865 | A | T | 10 | a0002c0002t0002g0013 a0002c0002t0002g0062 a0002c0002t0002g0091 others(7): Show |
11 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+5663A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823865 | |||||||
chr9:21823866 | A | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+5664A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823866 | |||||||
chr9:21823951 | G | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+5749G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823951 | |||||||
chr9:21823953 | T | C | 121 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(118): Show |
137 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.347+5751T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823953 | |||||||
chr9:21823975 | T | C | 1 | a0001c0003t0001g0052 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.347+5773T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21823975 | |||||||
chr9:21824050 | G | A | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.347+5848G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824050 | |||||||
chr9:21824103 | T | G | 1 | a0001c0001t0001g0253 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.347+5901T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824103 | |||||||
chr9:21824519 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.347+6317G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824519 | |||||||
chr9:21824534 | C | T | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+6332C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824534 | |||||||
chr9:21824608 | A | T | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+6406A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824608 | |||||||
chr9:21824611 | A | G | 1 | a0002c0002t0001g0090 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.347+6409A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824611 | |||||||
chr9:21824707 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0252 others(2): Show |
6 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.347+6505T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824707 | |||||||
chr9:21824755 | A | C | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6553A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824755 | |||||||
chr9:21824874 | C | G | 1 | a0002c0002t0002g0061 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.347+6672C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824874 | |||||||
chr9:21824876 | C | T | 1 | a0002c0002t0002g0061 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.347+6674C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824876 | |||||||
chr9:21824883 | C | T | 117 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(114): Show |
133 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.347+6681C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824883 | |||||||
chr9:21824895 | C | T | 3 | a0002c0002t0001g0088 a0002c0002t0001g0105 a0002c0002t0037g0089 |
3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.347+6693C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824895 | |||||||
chr9:21824906 | C | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6704C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824906 | |||||||
chr9:21824924 | T | C | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+6722T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824924 | |||||||
chr9:21824993 | G | A | 2 | a0001c0001t0003g0188 a0001c0001t0003g0189 |
2 | HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.347+6791G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21824993 | |||||||
chr9:21825041 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.347+6839A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825041 | |||||||
chr9:21825042 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.347+6840C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825042 | |||||||
chr9:21825068 | C | A | 1 | a0003c0005t0002g0009 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.347+6866C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825068 | |||||||
chr9:21825076 | T | C | 230 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0141 others(227): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.347+6874T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825076 | |||||||
chr9:21825101 | C | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+6899C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825101 | |||||||
chr9:21825146 | C | T | 1 | a0002c0002t0033g0070 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.347+6944C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825146 | |||||||
chr9:21825361 | C | A | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.347+7159C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825361 | |||||||
chr9:21825468 | A | G | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7266A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825468 | |||||||
chr9:21825471 | C | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0198 a0001c0001t0003g0017 others(1): Show |
5 | HG00140.hp2 HG02004.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+7269C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825471 | |||||||
chr9:21825485 | A | T | 1 | a0001c0007t0003g0136 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.347+7283A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825485 | |||||||
chr9:21825517 | A | G | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7315A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825517 | |||||||
chr9:21825575 | C | T | 3 | a0002c0002t0002g0007 a0002c0002t0002g0053 a0002c0002t0002g0054 |
4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+7373C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825575 | |||||||
chr9:21825718 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.347+7516A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825718 | |||||||
chr9:21825859 | T | C | 23 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(20): Show |
28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+7657T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825859 | |||||||
chr9:21825887 | G | C | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+7685G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825887 | |||||||
chr9:21825947 | G | GA | 104 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(101): Show |
116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.347+7747dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21825947 | ||||||
chr9:21825997 | A | G | 107 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(104): Show |
119 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.347+7795A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21825997 | |||||||
chr9:21826068 | C | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+7866C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826068 | |||||||
chr9:21826188 | C | CT | 6 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 others(3): Show |
6 | HG02622.hp2 HG02630.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.347+8001dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | ||||||
chr9:21826188 | CT | C | 175 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(172): Show |
196 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.347+8001delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | ||||||
chr9:21826188 | CTT | C | 8 | a0001c0001t0003g0153 a0001c0001t0003g0178 a0001c0001t0023g0058 others(5): Show |
8 | HG01123.hp1 HG01167.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.347+8000_347+8001d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826188 | ||||||
chr9:21826219 | T | G | 1 | a0001c0001t0014g0322 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.347+8017T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826219 | |||||||
chr9:21826227 | C | A | 2 | a0002c0002t0003g0065 a0002c0002t0003g0075 |
2 | HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.347+8025C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826227 | |||||||
chr9:21826287 | T | G | 1 | a0002c0002t0002g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.347+8085T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826287 | |||||||
chr9:21826388 | T | C | 89 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(86): Show |
99 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.347+8186T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826388 | |||||||
chr9:21826464 | C | T | 86 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(83): Show |
96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.347+8262C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826464 | |||||||
chr9:21826514 | A | T | 1 | a0002c0002t0016g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.347+8312A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826514 | |||||||
chr9:21826517 | A | G | 94 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(91): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.347+8315A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826517 | |||||||
chr9:21826518 | T | A | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+8316T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826518 | |||||||
chr9:21826539 | G | A | 211 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(208): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.347+8337G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826539 | |||||||
chr9:21826600 | G | A | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+8398G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826600 | |||||||
chr9:21826609 | T | TTTA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0034 others(31): Show |
41 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.347+8446_347+8448d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | T | TTTATTA | 6 | a0001c0001t0001g0327 a0001c0001t0010g0035 a0001c0001t0010g0326 others(3): Show |
7 | HG03041.hp1 NA18946.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.347+8443_347+8448d others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | T | TTTATTAT others(2): Show |
6 | a0001c0001t0001g0253 a0001c0001t0001g0265 a0001c0001t0001g0325 others(3): Show |
7 | HG01243.hp1 HG02630.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+8440_347+8448d others(11): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | TTTA | T | 73 | a0001c0001t0001g0022 a0001c0001t0001g0167 a0001c0001t0001g0209 others(70): Show |
81 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.347+8446_347+8448d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | TTTATTA | T | 8 | a0002c0002t0001g0077 a0002c0002t0002g0117 a0002c0002t0002g0118 others(5): Show |
8 | HG00438.hp2 HG00609.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.347+8443_347+8448d others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | TTTATTAT others(2): Show |
T | 90 | a0002c0002t0001g0074 a0002c0002t0001g0083 a0002c0002t0001g0090 others(87): Show |
105 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.347+8440_347+8448d others(11): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826609 | TTTATTAT others(11): Show |
T | 15 | a0001c0001t0009g0201 a0002c0002t0002g0056 a0002c0002t0002g0061 others(12): Show |
15 | HG00544.hp1 HG00673.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+8431_347+8448d others(20): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826609 | ||||||
chr9:21826621 | A | ATTATTG | 17 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
18 | HG01109.hp1 HG01123.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.347+8424_347+8425i others(8): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826621 | ||||||
chr9:21826621 | A | T | 2 | a0002c0002t0013g0010 a0002c0002t0013g0121 |
3 | NA18957.hp2 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.347+8419A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826621 | |||||||
chr9:21826624 | A | ATTG | 67 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0174 others(64): Show |
76 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.347+8424_347+8425i others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21826624 | ||||||
chr9:21826627 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.347+8425A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826627 | |||||||
chr9:21826630 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.347+8428A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826630 | |||||||
chr9:21826632 | T | G | 1 | a0002c0002t0011g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.347+8430T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826632 | |||||||
chr9:21826690 | A | C | 1 | a0001c0001t0023g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.347+8488A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826690 | |||||||
chr9:21826841 | G | A | 83 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(80): Show |
94 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.347+8639G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826841 | |||||||
chr9:21826845 | G | T | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.347+8643G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826845 | |||||||
chr9:21826854 | G | A | 1 | a0002c0002t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.347+8652G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826854 | |||||||
chr9:21826941 | G | T | 94 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(91): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.347+8739G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21826941 | |||||||
chr9:21827044 | T | A | 1 | a0001c0001t0009g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.347+8842T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827044 | |||||||
chr9:21827070 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.347+8868C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827070 | |||||||
chr9:21827169 | G | A | 1 | a0002c0002t0003g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.347+8967G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827169 | |||||||
chr9:21827193 | G | A | 23 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(20): Show |
28 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(25): Show |
intron_variant | MODIFIER | c.347+8991G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827193 | |||||||
chr9:21827284 | C | G | 1 | a0001c0001t0001g0265 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+9082C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827284 | |||||||
chr9:21827287 | C | G | 2 | a0001c0001t0004g0131 a0001c0001t0012g0130 |
2 | HG02257.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347+9085C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827287 | |||||||
chr9:21827407 | A | G | 94 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(91): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.347+9205A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827407 | |||||||
chr9:21827485 | A | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.347+9283A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827485 | |||||||
chr9:21827527 | T | G | 5 | a0001c0001t0003g0187 a0001c0001t0003g0191 a0001c0001t0003g0196 others(2): Show |
5 | HG02055.hp1 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+9325T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827527 | |||||||
chr9:21827913 | A | G | 3 | a0002c0002t0032g0068 a0002c0002t0033g0070 a0002c0002t0036g0069 |
3 | HG03041.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.347+9711A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827913 | |||||||
chr9:21827993 | G | A | 228 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(225): Show |
256 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.347+9791G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21827993 | |||||||
chr9:21828111 | A | C | 94 | a0002c0002t0001g0074 a0002c0002t0001g0077 a0002c0002t0001g0083 others(91): Show |
105 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.348-9797A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828111 | |||||||
chr9:21828243 | T | C | 231 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(228): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.348-9665T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828243 | |||||||
chr9:21828248 | G | A | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-9660G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828248 | |||||||
chr9:21828255 | G | A | 1 | a0002c0002t0032g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348-9653G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828255 | |||||||
chr9:21828315 | A | C | 1 | a0001c0001t0019g0241 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.348-9593A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828315 | |||||||
chr9:21828360 | G | A | 1 | a0002c0002t0036g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.348-9548G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828360 | |||||||
chr9:21828502 | C | T | 1 | a0001c0001t0035g0321 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.348-9406C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828502 | |||||||
chr9:21828543 | T | C | 3 | a0001c0001t0010g0035 a0001c0001t0010g0326 a0001c0001t0035g0321 |
4 | NA18948.hp1 NA18990.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-9365T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828543 | |||||||
chr9:21828618 | T | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0215 others(2): Show |
6 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-9290T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828618 | |||||||
chr9:21828663 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.348-9245G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828663 | |||||||
chr9:21828959 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.348-8949A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21828959 | |||||||
chr9:21829059 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.348-8849C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829059 | |||||||
chr9:21829065 | T | A | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-8843T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829065 | |||||||
chr9:21829111 | A | G | 1 | a0001c0003t0001g0050 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.348-8797A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829111 | |||||||
chr9:21829114 | G | C | 3 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 |
3 | HG02622.hp2 HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-8794G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829114 | |||||||
chr9:21829118 | C | T | 28 | a0001c0001t0004g0131 a0001c0001t0012g0130 a0002c0002t0003g0302 others(25): Show |
33 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.348-8790C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829118 | |||||||
chr9:21829129 | T | A | 1 | a0002c0002t0004g0298 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-8779T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829129 | |||||||
chr9:21829159 | A | C | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8749A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829159 | |||||||
chr9:21829273 | G | A | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8635G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829273 | |||||||
chr9:21829358 | G | A | 1 | a0002c0002t0001g0116 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.348-8550G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829358 | |||||||
chr9:21829417 | GT | G | 203 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(200): Show |
229 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.348-8479delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21829417 | ||||||
chr9:21829426 | T | TG | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-8482_348-8481i others(3): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829426 | |||||||
chr9:21829508 | T | C | 26 | a0002c0002t0003g0302 a0002c0002t0003g0314 a0002c0002t0004g0003 others(23): Show |
31 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.348-8400T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829508 | |||||||
chr9:21829553 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.348-8355G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829553 | |||||||
chr9:21829605 | T | A | 81 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(78): Show |
91 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.348-8303T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829605 | |||||||
chr9:21829629 | G | GA | 30 | a0001c0001t0005g0245 a0001c0001t0009g0152 a0001c0001t0009g0201 others(27): Show |
35 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(32): Show |
intron_variant | MODIFIER | c.348-8266dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21829629 | ||||||
chr9:21829720 | G | T | 1 | a0002c0002t0002g0094 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.348-8188G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829720 | |||||||
chr9:21829820 | T | G | 1 | a0002c0002t0016g0139 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.348-8088T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829820 | |||||||
chr9:21829974 | A | G | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-7934A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21829974 | |||||||
chr9:21830132 | C | G | 1 | a0002c0002t0004g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.348-7776C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830132 | |||||||
chr9:21830158 | A | G | 82 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(79): Show |
92 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.348-7750A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830158 | |||||||
chr9:21830163 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.348-7745G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830163 | |||||||
chr9:21830268 | A | G | 4 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0024g0197 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-7640A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830268 | |||||||
chr9:21830438 | C | T | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.348-7470C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830438 | |||||||
chr9:21830444 | C | A | 1 | a0001c0003t0001g0043 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.348-7464C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830444 | |||||||
chr9:21830467 | A | G | 2 | a0001c0001t0002g0290 a0001c0001t0040g0291 |
2 | HG02258.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.348-7441A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830467 | |||||||
chr9:21830480 | G | A | 12 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
13 | HG01109.hp1 HG01346.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.348-7428G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830480 | |||||||
chr9:21830542 | T | G | 4 | a0002c0002t0004g0295 a0002c0002t0004g0296 a0002c0002t0004g0300 others(1): Show |
4 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-7366T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830542 | |||||||
chr9:21830554 | A | G | 4 | a0001c0001t0023g0058 a0001c0001t0023g0147 a0001c0010t0009g0057 others(1): Show |
4 | HG01123.hp1 HG02055.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-7354A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830554 | |||||||
chr9:21830569 | G | A | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-7339G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830569 | |||||||
chr9:21830627 | T | G | 1 | a0001c0001t0003g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.348-7281T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830627 | |||||||
chr9:21830659 | C | G | 1 | a0001c0001t0001g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.348-7249C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830659 | |||||||
chr9:21830661 | C | G | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-7247C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830661 | |||||||
chr9:21830751 | A | G | 1 | a0002c0002t0011g0076 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.348-7157A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830751 | |||||||
chr9:21830894 | C | T | 1 | a0001c0001t0012g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.348-7014C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830894 | |||||||
chr9:21830945 | T | C | 2 | a0001c0001t0017g0021 a0001c0001t0017g0217 |
3 | NA18969.hp1 NA19006.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.348-6963T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21830945 | |||||||
chr9:21830954 | A | AATGAGAT | 13 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
14 | HG00323.hp1 HG01109.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-6953_348-6947d others(9): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21830954 | ||||||
chr9:21831031 | T | G | 3 | a0001c0001t0001g0267 a0001c0001t0003g0213 a0001c0001t0011g0214 |
3 | HG00323.hp2 HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.348-6877T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831031 | |||||||
chr9:21831044 | A | G | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348-6864A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831044 | |||||||
chr9:21831071 | C | T | 3 | a0001c0001t0003g0016 a0001c0007t0003g0135 a0001c0007t0003g0136 |
4 | HG01433.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-6837C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831071 | |||||||
chr9:21831344 | TG | T | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-6563delG | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831344 | |||||||
chr9:21831380 | G | A | 1 | a0001c0001t0009g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.348-6528G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831380 | |||||||
chr9:21831457 | G | A | 17 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(14): Show |
19 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.348-6451G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831457 | |||||||
chr9:21831495 | AT | A | 133 | a0001c0001t0001g0029 a0001c0001t0001g0140 a0001c0001t0001g0141 others(130): Show |
150 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.348-6401delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831495 | ||||||
chr9:21831630 | A | G | 110 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(107): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.348-6278A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831630 | |||||||
chr9:21831636 | T | C | 2 | a0001c0001t0010g0035 a0001c0001t0035g0321 |
3 | NA18990.hp2 NA19010.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.348-6272T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831636 | |||||||
chr9:21831783 | T | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03017.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.348-6125T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831783 | |||||||
chr9:21831785 | A | AT | 21 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(18): Show |
23 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.348-6109dupT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831785 | ||||||
chr9:21831785 | AT | A | 86 | a0001c0001t0001g0319 a0001c0001t0002g0151 a0001c0001t0014g0268 others(83): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.348-6109delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21831785 | ||||||
chr9:21831786 | T | C | 3 | a0002c0002t0016g0137 a0002c0002t0016g0138 a0002c0002t0016g0139 |
3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.348-6122T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831786 | |||||||
chr9:21831980 | A | G | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-5928A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21831980 | |||||||
chr9:21832227 | T | A | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-5681T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832227 | |||||||
chr9:21832358 | T | C | 1 | a0001c0001t0002g0031 | 2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.348-5550T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832358 | |||||||
chr9:21832541 | G | A | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-5367G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832541 | |||||||
chr9:21832551 | T | C | 1 | a0001c0001t0003g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.348-5357T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832551 | |||||||
chr9:21832635 | G | T | 1 | a0002c0002t0004g0312 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.348-5273G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832635 | |||||||
chr9:21832738 | C | T | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-5170C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832738 | |||||||
chr9:21832743 | A | G | 102 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(99): Show |
117 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.348-5165A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832743 | |||||||
chr9:21832786 | T | C | 1 | a0002c0002t0002g0092 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.348-5122T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832786 | |||||||
chr9:21832925 | A | C | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4983A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21832925 | |||||||
chr9:21833047 | T | C | 101 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(98): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.348-4861T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833047 | |||||||
chr9:21833085 | C | T | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4823C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833085 | |||||||
chr9:21833339 | T | C | 232 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(229): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.348-4569T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833339 | |||||||
chr9:21833421 | G | T | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-4487G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833421 | |||||||
chr9:21833474 | A | G | 1 | a0001c0007t0003g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.348-4434A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833474 | |||||||
chr9:21833619 | C | T | 1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.348-4289C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833619 | |||||||
chr9:21833639 | G | A | 1 | a0002c0002t0032g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.348-4269G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833639 | |||||||
chr9:21833660 | A | G | 103 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(100): Show |
118 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.348-4248A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833660 | |||||||
chr9:21833685 | T | C | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348-4223T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833685 | |||||||
chr9:21833710 | G | A | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4198G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833710 | |||||||
chr9:21833763 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.348-4145T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833763 | |||||||
chr9:21833785 | T | C | 2 | a0001c0001t0012g0130 a0001c0001t0031g0148 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.348-4123T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833785 | |||||||
chr9:21833814 | G | A | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.348-4094G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833814 | |||||||
chr9:21833843 | T | C | 2 | a0001c0001t0009g0152 a0002c0002t0051g0299 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.348-4065T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833843 | |||||||
chr9:21833869 | C | T | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-4039C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833869 | |||||||
chr9:21833884 | A | G | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-4024A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833884 | |||||||
chr9:21833921 | T | C | 1 | a0001c0001t0005g0239 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.348-3987T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833921 | |||||||
chr9:21833994 | A | G | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.348-3914A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21833994 | |||||||
chr9:21834017 | A | G | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-3891A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834017 | |||||||
chr9:21834031 | T | C | 1 | a0002c0002t0004g0298 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.348-3877T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834031 | |||||||
chr9:21834211 | T | C | 90 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(87): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.348-3697T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834211 | |||||||
chr9:21834317 | A | T | 3 | a0001c0001t0008g0132 a0001c0001t0008g0133 a0001c0001t0008g0134 |
3 | HG02257.hp2 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.348-3591A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834317 | |||||||
chr9:21834382 | A | G | 2 | a0002c0002t0003g0086 a0002c0002t0003g0087 |
2 | NA18986.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.348-3526A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834382 | |||||||
chr9:21834544 | C | G | 2 | a0001c0001t0018g0027 a0001c0001t0018g0276 |
3 | HG00140.hp1 HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.348-3364C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834544 | |||||||
chr9:21834601 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0041g0040 |
3 | HG01515.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.348-3307C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834601 | |||||||
chr9:21834630 | A | C | 2 | a0001c0001t0023g0058 a0001c0001t0023g0147 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.348-3278A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834630 | |||||||
chr9:21834642 | T | C | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-3266T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834642 | |||||||
chr9:21834813 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0229 |
2 | NA18998.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.348-3095A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834813 | |||||||
chr9:21834823 | A | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-3085A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834823 | |||||||
chr9:21834938 | G | A | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.348-2970G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834938 | |||||||
chr9:21834948 | A | C | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2960A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834948 | |||||||
chr9:21834969 | C | T | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2939C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21834969 | |||||||
chr9:21835057 | A | C | 1 | a0001c0001t0001g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.348-2851A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835057 | |||||||
chr9:21835115 | T | C | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-2793T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835115 | |||||||
chr9:21835119 | G | C | 4 | a0001c0001t0009g0201 a0001c0001t0023g0058 a0001c0001t0023g0147 others(1): Show |
4 | HG02055.hp2 HG02630.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-2789G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835119 | |||||||
chr9:21835144 | C | T | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-2764C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835144 | |||||||
chr9:21835225 | C | T | 1 | a0002c0002t0016g0137 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.348-2683C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835225 | |||||||
chr9:21835242 | A | C | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-2666A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835242 | |||||||
chr9:21835330 | C | G | 1 | a0002c0002t0002g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.348-2578C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835330 | |||||||
chr9:21835454 | A | AGAAATAT others(31): Show |
1 | a0001c0003t0001g0051 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.348-2442_348-2405d others(40): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21835454 | ||||||
chr9:21835558 | C | G | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.348-2350C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835558 | |||||||
chr9:21835640 | T | C | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.348-2268T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835640 | |||||||
chr9:21835784 | G | T | 1 | a0001c0001t0005g0238 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.348-2124G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835784 | |||||||
chr9:21835859 | C | G | 3 | a0001c0001t0008g0132 a0001c0001t0008g0133 a0001c0001t0008g0134 |
3 | HG02257.hp2 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.348-2049C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835859 | |||||||
chr9:21835969 | C | T | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.348-1939C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21835969 | |||||||
chr9:21836062 | C | T | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1846C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836062 | |||||||
chr9:21836254 | G | C | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.348-1654G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836254 | |||||||
chr9:21836294 | C | T | 5 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0174 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.348-1614C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836294 | |||||||
chr9:21836469 | A | C | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.348-1439A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836469 | |||||||
chr9:21836521 | T | C | 1 | a0002c0002t0044g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.348-1387T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836521 | |||||||
chr9:21836586 | A | G | 3 | a0002c0002t0001g0088 a0002c0002t0001g0105 a0002c0002t0037g0089 |
3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.348-1322A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836586 | |||||||
chr9:21836802 | G | A | 2 | a0002c0002t0012g0315 a0002c0002t0012g0316 |
2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.348-1106G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21836802 | |||||||
chr9:21837005 | C | A | 1 | a0001c0001t0003g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.348-903C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837005 | |||||||
chr9:21837145 | GT | G | 99 | a0001c0001t0001g0319 a0001c0001t0002g0151 a0001c0001t0002g0285 others(96): Show |
110 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.348-759delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr9 | 21837145 | ||||||
chr9:21837206 | A | G | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-702A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837206 | |||||||
chr9:21837427 | C | T | 3 | a0002c0002t0016g0137 a0002c0002t0016g0138 a0002c0002t0016g0139 |
3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.348-481C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837427 | |||||||
chr9:21837557 | G | A | 1 | a0002c0002t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.348-351G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837557 | |||||||
chr9:21837579 | T | C | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.348-329T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837579 | |||||||
chr9:21837663 | C | T | 1 | a0001c0001t0014g0322 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.348-245C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837663 | |||||||
chr9:21837700 | C | T | 8 | a0001c0001t0003g0183 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
8 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-208C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837700 | |||||||
chr9:21837845 | C | T | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-63C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 4/7 | chr9 | 21837845 | |||||||
chr9:21838146 | A | G | 100 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(97): Show |
111 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.450+136A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838146 | |||||||
chr9:21838180 | C | A | 8 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
8 | HG00323.hp1 HG01109.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+170C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838180 | |||||||
chr9:21838226 | A | G | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.450+216A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838226 | |||||||
chr9:21838342 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.450+332C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838342 | |||||||
chr9:21838378 | T | G | 1 | a0001c0001t0011g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.450+368T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838378 | |||||||
chr9:21838468 | G | A | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+458G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838468 | |||||||
chr9:21838675 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0292 others(1): Show |
4 | NA18941.hp2 NA18948.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+665A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838675 | |||||||
chr9:21838820 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.450+810A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838820 | |||||||
chr9:21838837 | G | A | 2 | a0001c0001t0003g0153 a0001c0001t0003g0175 |
2 | NA19003.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.450+827G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21838837 | |||||||
chr9:21839019 | A | C | 1 | a0002c0002t0007g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.450+1009A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839019 | |||||||
chr9:21839173 | G | GTT | 11 | a0001c0001t0001g0165 a0001c0001t0003g0153 a0001c0001t0003g0161 others(8): Show |
11 | HG01975.hp2 HG02015.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+1177_450+1178d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839173 | ||||||
chr9:21839173 | G | GTTT | 96 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(93): Show |
111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.450+1176_450+1178d others(5): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839173 | ||||||
chr9:21839173 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.450+1163G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839173 | |||||||
chr9:21839188 | T | A | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1178T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839188 | |||||||
chr9:21839188 | TA | T | 5 | a0001c0001t0014g0264 a0002c0002t0002g0064 a0002c0002t0003g0087 others(2): Show |
5 | HG01069.hp2 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+1184delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21839188 | ||||||
chr9:21839189 | A | T | 216 | a0001c0001t0001g0026 a0001c0001t0001g0140 a0001c0001t0001g0141 others(213): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.450+1179A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839189 | |||||||
chr9:21839190 | A | T | 4 | a0001c0001t0002g0171 a0001c0001t0046g0159 a0002c0002t0002g0085 others(1): Show |
4 | HG00673.hp2 HG01169.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1180A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839190 | |||||||
chr9:21839255 | G | A | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+1245G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839255 | |||||||
chr9:21839376 | G | A | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+1366G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839376 | |||||||
chr9:21839410 | G | A | 2 | a0002c0002t0002g0078 a0002c0002t0002g0128 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.450+1400G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839410 | |||||||
chr9:21839533 | T | A | 7 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0215 others(4): Show |
8 | NA18947.hp2 NA18950.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+1523T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839533 | |||||||
chr9:21839541 | A | T | 2 | a0002c0002t0001g0124 a0002c0002t0001g0127 |
2 | NA18983.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.450+1531A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839541 | |||||||
chr9:21839770 | A | T | 1 | a0001c0003t0001g0043 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.450+1760A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839770 | |||||||
chr9:21839796 | T | G | 4 | a0001c0001t0008g0132 a0001c0001t0008g0133 a0001c0001t0008g0134 others(1): Show |
4 | HG02257.hp2 HG02818.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1786T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21839796 | |||||||
chr9:21840064 | A | G | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.450+2054A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840064 | |||||||
chr9:21840148 | C | A | 1 | a0001c0001t0020g0149 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+2138C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840148 | |||||||
chr9:21840194 | C | G | 99 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(96): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2184C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840194 | |||||||
chr9:21840221 | C | CA | 20 | a0001c0001t0001g0231 a0001c0001t0001g0319 a0001c0001t0003g0212 others(17): Show |
20 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+2225dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21840221 | ||||||
chr9:21840221 | C | CAA | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+2224_450+2225d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21840221 | ||||||
chr9:21840276 | C | T | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2266C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840276 | |||||||
chr9:21840277 | G | A | 1 | a0002c0002t0044g0304 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.450+2267G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840277 | |||||||
chr9:21840299 | A | G | 101 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(98): Show |
112 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+2289A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840299 | |||||||
chr9:21840388 | C | T | 97 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(94): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+2378C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840388 | |||||||
chr9:21840495 | A | G | 1 | a0001c0001t0012g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.450+2485A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840495 | |||||||
chr9:21840532 | G | C | 4 | a0001c0001t0009g0152 a0002c0002t0004g0066 a0002c0002t0004g0067 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2522G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840532 | |||||||
chr9:21840761 | A | G | 99 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(96): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2751A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840761 | |||||||
chr9:21840778 | G | A | 99 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(96): Show |
110 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.450+2768G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840778 | |||||||
chr9:21840835 | G | T | 56 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0167 others(53): Show |
65 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.450+2825G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840835 | |||||||
chr9:21840843 | C | T | 99 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(96): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.450+2833C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840843 | |||||||
chr9:21840966 | C | T | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+2956C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21840966 | |||||||
chr9:21841033 | C | T | 1 | a0001c0001t0009g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.450+3023C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841033 | |||||||
chr9:21841072 | A | G | 2 | a0001c0001t0023g0058 a0001c0001t0023g0147 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.450+3062A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841072 | |||||||
chr9:21841119 | C | T | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+3109C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841119 | |||||||
chr9:21841219 | A | G | 18 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
20 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+3209A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841219 | |||||||
chr9:21841370 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+3360G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841370 | |||||||
chr9:21841484 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.450+3474C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841484 | |||||||
chr9:21841659 | C | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 |
3 | NA18966.hp2 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.450+3649C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841659 | |||||||
chr9:21841909 | A | G | 6 | a0001c0001t0009g0201 a0001c0010t0009g0057 a0002c0002t0012g0315 others(3): Show |
6 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+3899A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841909 | |||||||
chr9:21841956 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0198 others(1): Show |
4 | HG00323.hp1 HG01346.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+3946C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21841956 | |||||||
chr9:21842033 | A | G | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+4023A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842033 | |||||||
chr9:21842101 | A | C | 1 | a0002c0004t0001g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.450+4091A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842101 | |||||||
chr9:21842155 | G | A | 37 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(34): Show |
43 | HG00323.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.450+4145G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842155 | |||||||
chr9:21842178 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0023g0058 a0001c0001t0023g0147 |
3 | HG02055.hp2 HG02723.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.450+4168C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842178 | |||||||
chr9:21842217 | C | G | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+4207C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842217 | |||||||
chr9:21842226 | G | A | 97 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(94): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.450+4216G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842226 | |||||||
chr9:21842269 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.450+4259A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842269 | |||||||
chr9:21842301 | G | C | 96 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(93): Show |
111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.450+4291G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842301 | |||||||
chr9:21842380 | A | G | 2 | a0001c0001t0009g0201 a0001c0001t0024g0197 |
2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.450+4370A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842380 | |||||||
chr9:21842506 | A | T | 1 | a0001c0001t0034g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.450+4496A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842506 | |||||||
chr9:21842631 | C | T | 7 | a0001c0001t0020g0149 a0001c0001t0031g0148 a0001c0010t0009g0057 others(4): Show |
7 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+4621C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842631 | |||||||
chr9:21842677 | G | T | 1 | a0001c0001t0001g0034 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.450+4667G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842677 | |||||||
chr9:21842734 | A | G | 227 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(224): Show |
255 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.450+4724A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842734 | |||||||
chr9:21842853 | G | A | 5 | a0001c0010t0009g0057 a0002c0002t0012g0315 a0002c0002t0012g0316 others(2): Show |
5 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+4843G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21842853 | |||||||
chr9:21843395 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.450+5385A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843395 | |||||||
chr9:21843400 | C | G | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+5390C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843400 | |||||||
chr9:21843424 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.450+5414A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843424 | |||||||
chr9:21843425 | T | C | 1 | a0002c0002t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.450+5415T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843425 | |||||||
chr9:21843465 | G | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.450+5455G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843465 | |||||||
chr9:21843533 | A | T | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.450+5523A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843533 | |||||||
chr9:21843573 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450+5563T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843573 | |||||||
chr9:21843630 | A | G | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+5620A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843630 | |||||||
chr9:21843737 | A | G | 37 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(34): Show |
43 | HG00323.hp1 HG01109.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.450+5727A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843737 | |||||||
chr9:21843827 | C | A | 88 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(85): Show |
99 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.450+5817C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843827 | |||||||
chr9:21843843 | A | G | 104 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(101): Show |
115 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.450+5833A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21843843 | |||||||
chr9:21844300 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.450+6290C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844300 | |||||||
chr9:21844449 | T | C | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.450+6439T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844449 | |||||||
chr9:21844602 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.450+6592C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844602 | |||||||
chr9:21844614 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.450+6604A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844614 | |||||||
chr9:21844644 | A | G | 106 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0319 others(103): Show |
117 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.450+6634A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844644 | |||||||
chr9:21844686 | A | G | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.450+6676A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844686 | |||||||
chr9:21844762 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.450+6752C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844762 | |||||||
chr9:21844773 | A | G | 107 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0281 others(104): Show |
118 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.450+6763A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844773 | |||||||
chr9:21844801 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0272 a0001c0001t0001g0286 |
4 | HG03098.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+6791A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844801 | |||||||
chr9:21844826 | T | A | 1 | a0001c0001t0003g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.450+6816T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844826 | |||||||
chr9:21844827 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.450+6817C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844827 | |||||||
chr9:21844827 | C | T | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+6817C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844827 | |||||||
chr9:21844831 | A | T | 2 | a0001c0001t0020g0199 a0001c0001t0024g0190 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.450+6821A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844831 | |||||||
chr9:21844847 | C | T | 6 | a0001c0010t0009g0057 a0002c0002t0001g0077 a0002c0002t0022g0113 others(3): Show |
6 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.450+6837C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844847 | |||||||
chr9:21844952 | A | G | 17 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(14): Show |
19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+6942A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844952 | |||||||
chr9:21844955 | C | T | 3 | a0001c0001t0009g0201 a0001c0001t0023g0058 a0001c0001t0023g0147 |
3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.450+6945C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21844955 | |||||||
chr9:21845018 | G | A | 1 | a0002c0002t0002g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.450+7008G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845018 | |||||||
chr9:21845030 | C | CA | 193 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(190): Show |
218 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.450+7035dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845030 | ||||||
chr9:21845030 | C | CAA | 12 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0042g0172 others(9): Show |
13 | HG01123.hp2 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+7034_450+7035d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845030 | ||||||
chr9:21845053 | A | G | 17 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0001g0243 others(14): Show |
19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+7043A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845053 | |||||||
chr9:21845056 | A | G | 1 | a0001c0003t0001g0049 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.450+7046A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845056 | |||||||
chr9:21845188 | C | G | 1 | a0002c0002t0004g0297 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.450+7178C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845188 | |||||||
chr9:21845229 | G | A | 1 | a0002c0002t0002g0080 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.450+7219G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845229 | |||||||
chr9:21845265 | C | T | 17 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0002g0155 others(14): Show |
19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.450+7255C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845265 | |||||||
chr9:21845309 | A | G | 58 | a0001c0001t0001g0158 a0001c0001t0002g0155 a0001c0001t0003g0002 others(55): Show |
67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.450+7299A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845309 | |||||||
chr9:21845342 | A | G | 3 | a0001c0001t0009g0201 a0001c0001t0023g0058 a0001c0001t0023g0147 |
3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.450+7332A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845342 | |||||||
chr9:21845346 | A | G | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.450+7336A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845346 | |||||||
chr9:21845578 | G | T | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.450+7568G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845578 | |||||||
chr9:21845659 | C | T | 1 | a0002c0002t0004g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.450+7649C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845659 | |||||||
chr9:21845739 | G | C | 209 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(206): Show |
232 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.450+7729G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845739 | |||||||
chr9:21845752 | T | TA | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+7753dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21845752 | ||||||
chr9:21845981 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.450+7971C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21845981 | |||||||
chr9:21846095 | A | G | 1 | a0001c0001t0003g0163 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.450+8085A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846095 | |||||||
chr9:21846167 | A | T | 25 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0243 others(22): Show |
30 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.450+8157A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846167 | |||||||
chr9:21846169 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0229 |
2 | NA18998.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.450+8159A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846169 | |||||||
chr9:21846188 | G | A | 2 | a0001c0001t0009g0152 a0002c0002t0051g0299 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.450+8178G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846188 | |||||||
chr9:21846286 | A | G | 98 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0020 others(95): Show |
108 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.450+8276A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846286 | |||||||
chr9:21846328 | C | T | 93 | a0001c0001t0002g0020 a0001c0001t0002g0151 a0001c0001t0002g0171 others(90): Show |
103 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.451-8303C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846328 | |||||||
chr9:21846352 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.451-8279G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846352 | |||||||
chr9:21846417 | GA | G | 114 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(111): Show |
131 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.451-8202delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21846417 | ||||||
chr9:21846433 | C | T | 1 | a0001c0001t0011g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.451-8198C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846433 | |||||||
chr9:21846468 | T | A | 1 | a0002c0002t0004g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.451-8163T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846468 | |||||||
chr9:21846480 | A | G | 1 | a0001c0001t0003g0187 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.451-8151A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846480 | |||||||
chr9:21846493 | C | T | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-8138C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846493 | |||||||
chr9:21846728 | A | G | 215 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(212): Show |
242 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.451-7903A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846728 | |||||||
chr9:21846820 | T | C | 1 | a0001c0001t0001g0319 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.451-7811T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846820 | |||||||
chr9:21846848 | A | G | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-7783A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846848 | |||||||
chr9:21846854 | G | T | 1 | a0001c0001t0003g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.451-7777G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846854 | |||||||
chr9:21846870 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451-7761G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21846870 | |||||||
chr9:21847131 | G | A | 3 | a0002c0002t0001g0088 a0002c0002t0001g0105 a0002c0002t0037g0089 |
3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.451-7500G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847131 | |||||||
chr9:21847221 | C | T | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7410C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847221 | |||||||
chr9:21847226 | T | C | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7405T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847226 | |||||||
chr9:21847236 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.451-7395C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847236 | |||||||
chr9:21847273 | A | G | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-7358A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847273 | |||||||
chr9:21847411 | G | C | 1 | a0001c0001t0001g0273 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.451-7220G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847411 | |||||||
chr9:21847573 | T | G | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-7058T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847573 | |||||||
chr9:21847581 | A | G | 2 | a0001c0001t0002g0285 a0001c0001t0014g0264 |
2 | HG01081.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.451-7050A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847581 | |||||||
chr9:21847584 | T | C | 2 | a0001c0010t0009g0057 a0004c0009t0009g0037 |
2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.451-7047T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847584 | |||||||
chr9:21847629 | A | G | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-7002A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21847629 | |||||||
chr9:21848250 | C | A | 4 | a0001c0001t0010g0035 a0001c0001t0010g0257 a0001c0001t0010g0326 others(1): Show |
5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-6381C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848250 | |||||||
chr9:21848255 | G | T | 25 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0243 others(22): Show |
30 | HG01168.hp1 HG01169.hp1 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.451-6376G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848255 | |||||||
chr9:21848285 | T | C | 3 | a0001c0001t0009g0201 a0001c0001t0023g0058 a0001c0001t0023g0147 |
3 | HG02055.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-6346T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848285 | |||||||
chr9:21848352 | G | A | 1 | a0001c0001t0012g0166 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.451-6279G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848352 | |||||||
chr9:21848380 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.451-6251G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848380 | |||||||
chr9:21848424 | T | TGATTTGG others(14): Show |
94 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0020 others(91): Show |
104 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.451-6202_451-6182d others(23): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21848424 | ||||||
chr9:21848532 | G | A | 58 | a0001c0001t0001g0158 a0001c0001t0002g0155 a0001c0001t0003g0002 others(55): Show |
67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.451-6099G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848532 | |||||||
chr9:21848745 | C | A | 84 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0020 others(81): Show |
94 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.451-5886C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848745 | |||||||
chr9:21848800 | C | T | 1 | a0002c0002t0004g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.451-5831C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848800 | |||||||
chr9:21848801 | G | A | 3 | a0001c0010t0009g0057 a0002c0002t0039g0294 a0004c0009t0009g0037 |
3 | HG01123.hp1 HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.451-5830G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21848801 | |||||||
chr9:21849058 | G | T | 1 | a0001c0001t0008g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451-5573G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849058 | |||||||
chr9:21849067 | A | T | 96 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0020 others(93): Show |
106 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.451-5564A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849067 | |||||||
chr9:21849094 | C | CAG | 218 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(215): Show |
245 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.451-5535_451-5534d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21849094 | ||||||
chr9:21849179 | G | C | 217 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(214): Show |
244 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(241): Show |
intron_variant | MODIFIER | c.451-5452G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849179 | |||||||
chr9:21849429 | A | G | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.451-5202A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849429 | |||||||
chr9:21849484 | C | T | 1 | a0002c0002t0003g0314 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.451-5147C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849484 | |||||||
chr9:21849564 | T | C | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-5067T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849564 | |||||||
chr9:21849759 | A | T | 1 | a0002c0002t0002g0084 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.451-4872A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849759 | |||||||
chr9:21849842 | A | G | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-4789A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849842 | |||||||
chr9:21849843 | T | A | 1 | a0001c0001t0001g0006 | 3 | NA18980.hp1 NA19011.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.451-4788T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849843 | |||||||
chr9:21849989 | T | C | 1 | a0001c0001t0006g0202 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.451-4642T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21849989 | |||||||
chr9:21850045 | C | G | 95 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0020 others(92): Show |
105 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.451-4586C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850045 | |||||||
chr9:21850055 | T | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-4576T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850055 | |||||||
chr9:21850148 | C | T | 3 | a0001c0001t0003g0173 a0001c0001t0003g0176 a0001c0001t0003g0177 |
3 | NA18985.hp2 NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.451-4483C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850148 | |||||||
chr9:21850526 | C | T | 1 | a0002c0002t0039g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.451-4105C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850526 | |||||||
chr9:21850597 | T | C | 5 | a0002c0002t0002g0085 a0002c0002t0002g0102 a0002c0002t0002g0318 others(2): Show |
5 | HG00673.hp2 HG04228.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.451-4034T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850597 | |||||||
chr9:21850625 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0283 |
4 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-4006G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850625 | |||||||
chr9:21850835 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.451-3796G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21850835 | |||||||
chr9:21851120 | C | T | 1 | a0001c0003t0001g0046 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.451-3511C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851120 | |||||||
chr9:21851158 | C | T | 94 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(91): Show |
104 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.451-3473C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851158 | |||||||
chr9:21851166 | G | A | 1 | a0001c0001t0005g0246 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.451-3465G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851166 | |||||||
chr9:21851245 | T | C | 2 | a0001c0001t0009g0152 a0002c0002t0051g0299 |
2 | HG02622.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.451-3386T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851245 | |||||||
chr9:21851247 | G | A | 1 | a0001c0001t0003g0331 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.451-3384G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851247 | |||||||
chr9:21851277 | G | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-3354G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851277 | |||||||
chr9:21851311 | CTG | C | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3318_451-3317d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21851311 | ||||||
chr9:21851434 | A | C | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3197A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851434 | |||||||
chr9:21851486 | G | T | 6 | a0001c0001t0012g0166 a0001c0010t0009g0057 a0002c0002t0012g0315 others(3): Show |
6 | HG01123.hp1 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.451-3145G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851486 | |||||||
chr9:21851506 | C | G | 92 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(89): Show |
102 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.451-3125C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851506 | |||||||
chr9:21851538 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451-3093C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851538 | |||||||
chr9:21851599 | G | T | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-3032G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851599 | |||||||
chr9:21851684 | G | A | 10 | a0001c0001t0003g0183 a0001c0001t0003g0186 a0001c0001t0003g0187 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-2947G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851684 | |||||||
chr9:21851688 | G | T | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-2943G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851688 | |||||||
chr9:21851693 | G | A | 2 | a0001c0001t0003g0221 a0001c0001t0003g0222 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.451-2938G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851693 | |||||||
chr9:21851771 | C | A | 1 | a0001c0001t0034g0182 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.451-2860C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851771 | |||||||
chr9:21851778 | G | A | 84 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(81): Show |
94 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.451-2853G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851778 | |||||||
chr9:21851832 | G | A | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2799G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851832 | |||||||
chr9:21851839 | C | A | 99 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(96): Show |
114 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.451-2792C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21851839 | |||||||
chr9:21852074 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.451-2557C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852074 | |||||||
chr9:21852182 | G | T | 101 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(98): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.451-2449G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852182 | |||||||
chr9:21852192 | T | C | 101 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(98): Show |
116 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.451-2439T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852192 | |||||||
chr9:21852314 | C | T | 2 | a0001c0010t0009g0057 a0004c0009t0009g0037 |
2 | HG01123.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.451-2317C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852314 | |||||||
chr9:21852359 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.451-2272G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852359 | |||||||
chr9:21852419 | A | G | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-2212A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852419 | |||||||
chr9:21852427 | T | C | 1 | a0001c0001t0012g0130 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.451-2204T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852427 | |||||||
chr9:21852483 | G | A | 1 | a0001c0001t0015g0181 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.451-2148G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852483 | |||||||
chr9:21852509 | C | CA | 72 | a0001c0001t0001g0158 a0001c0001t0001g0227 a0001c0001t0002g0155 others(69): Show |
82 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.451-2105dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | ||||||
chr9:21852509 | C | CAA | 50 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(47): Show |
56 | HG00323.hp1 HG01074.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.451-2106_451-2105d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | ||||||
chr9:21852509 | CA | C | 81 | a0001c0001t0001g0220 a0001c0001t0001g0270 a0001c0001t0001g0271 others(78): Show |
90 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.451-2105delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852509 | ||||||
chr9:21852596 | G | A | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451-2035G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852596 | |||||||
chr9:21852629 | A | T | 3 | a0001c0001t0012g0166 a0002c0002t0012g0315 a0002c0002t0012g0316 |
3 | HG02109.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.451-2002A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852629 | |||||||
chr9:21852660 | TTATATAC others(1): Show |
T | 16 | a0001c0001t0002g0151 a0002c0002t0001g0074 a0002c0002t0001g0098 others(13): Show |
17 | HG02074.hp2 NA18940.hp1 NA18941.hp1 others(14): Show |
intron_variant | MODIFIER | c.451-1969_451-1962d others(10): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852660 | ||||||
chr9:21852672 | C | G | 1 | a0001c0001t0031g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.451-1959C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852672 | |||||||
chr9:21852698 | T | C | 3 | a0001c0001t0001g0158 a0001c0001t0003g0017 a0001c0001t0046g0159 |
4 | HG00140.hp2 HG02004.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1933T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852698 | |||||||
chr9:21852707 | G | GA | 12 | a0001c0001t0001g0029 a0001c0001t0001g0208 a0001c0001t0001g0247 others(9): Show |
13 | HG01099.hp2 HG01168.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.451-1910dupA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | ||||||
chr9:21852707 | G | GAA | 16 | a0001c0001t0001g0237 a0001c0001t0001g0242 a0001c0001t0005g0023 others(13): Show |
18 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.451-1911_451-1910d others(4): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | ||||||
chr9:21852707 | GA | G | 8 | a0001c0001t0004g0185 a0001c0010t0009g0057 a0002c0002t0002g0056 others(5): Show |
8 | HG00621.hp1 HG01123.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1910delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr9 | 21852707 | ||||||
chr9:21852853 | C | A | 93 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(90): Show |
103 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.451-1778C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852853 | |||||||
chr9:21852882 | T | C | 3 | a0002c0002t0016g0137 a0002c0002t0016g0138 a0002c0002t0016g0139 |
3 | HG01074.hp1 HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.451-1749T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21852882 | |||||||
chr9:21853034 | T | A | 1 | a0002c0002t0003g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.451-1597T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853034 | |||||||
chr9:21853105 | C | G | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-1526C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853105 | |||||||
chr9:21853222 | T | C | 218 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(215): Show |
245 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.451-1409T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853222 | |||||||
chr9:21853265 | G | A | 8 | a0002c0002t0004g0066 a0002c0002t0004g0067 a0002c0002t0004g0295 others(5): Show |
8 | HG01192.hp2 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.451-1366G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853265 | |||||||
chr9:21853277 | G | C | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-1354G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853277 | |||||||
chr9:21853340 | A | G | 105 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(102): Show |
120 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.451-1291A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853340 | |||||||
chr9:21853410 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.451-1221T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853410 | |||||||
chr9:21853456 | G | A | 3 | a0001c0001t0012g0166 a0002c0002t0012g0315 a0002c0002t0012g0316 |
3 | HG02109.hp2 HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.451-1175G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853456 | |||||||
chr9:21853553 | G | A | 1 | a0002c0002t0002g0102 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.451-1078G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853553 | |||||||
chr9:21853630 | G | C | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-1001G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853630 | |||||||
chr9:21853732 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.451-899A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853732 | |||||||
chr9:21853898 | T | C | 2 | a0001c0001t0009g0201 a0001c0001t0023g0058 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.451-733T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853898 | |||||||
chr9:21853941 | T | C | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.451-690T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21853941 | |||||||
chr9:21854014 | C | T | 1 | a0001c0001t0010g0326 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.451-617C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854014 | |||||||
chr9:21854043 | A | G | 1 | a0002c0002t0032g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.451-588A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854043 | |||||||
chr9:21854077 | C | T | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.451-554C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854077 | |||||||
chr9:21854160 | T | C | 55 | a0001c0001t0001g0158 a0001c0001t0003g0002 a0001c0001t0003g0005 others(52): Show |
64 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.451-471T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854160 | |||||||
chr9:21854200 | A | G | 97 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(94): Show |
107 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.451-431A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854200 | |||||||
chr9:21854216 | C | G | 4 | a0001c0001t0004g0131 a0002c0002t0004g0307 a0002c0002t0004g0308 others(1): Show |
4 | HG02257.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-415C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854216 | |||||||
chr9:21854275 | A | G | 2 | a0001c0001t0024g0197 a0001c0001t0031g0148 |
2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.451-356A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854275 | |||||||
chr9:21854363 | G | A | 1 | a0001c0001t0014g0322 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.451-268G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854363 | |||||||
chr9:21854510 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.451-121G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854510 | |||||||
chr9:21854563 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.451-68G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 5/7 | chr9 | 21854563 | |||||||
chr9:21854921 | A | G | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+51A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21854921 | |||||||
chr9:21854970 | C | T | 1 | a0001c0001t0008g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.690+100C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21854970 | |||||||
chr9:21855014 | T | C | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+144T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855014 | |||||||
chr9:21855017 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0174 |
3 | HG01891.hp2 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.690+147G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855017 | |||||||
chr9:21855039 | G | A | 94 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(91): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.690+169G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855039 | |||||||
chr9:21855097 | G | T | 211 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(208): Show |
238 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.690+227G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855097 | |||||||
chr9:21855119 | C | G | 4 | a0001c0003t0001g0004 a0001c0003t0001g0046 a0001c0003t0001g0049 others(1): Show |
6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+249C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855119 | |||||||
chr9:21855267 | C | T | 1 | a0001c0001t0025g0033 | 2 | NA19058.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.690+397C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855267 | |||||||
chr9:21855309 | A | G | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+439A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855309 | |||||||
chr9:21855346 | G | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0269 |
2 | HG00738.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.690+476G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855346 | |||||||
chr9:21855347 | G | A | 17 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(14): Show |
19 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.690+477G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855347 | |||||||
chr9:21855373 | A | G | 1 | a0001c0003t0001g0225 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.690+503A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855373 | |||||||
chr9:21855447 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.690+577T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855447 | |||||||
chr9:21855453 | G | C | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+583G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855453 | |||||||
chr9:21855593 | C | T | 14 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(11): Show |
16 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.690+723C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855593 | |||||||
chr9:21855673 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0041g0040 |
3 | HG01515.hp1 HG01517.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.690+803G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855673 | |||||||
chr9:21855688 | G | A | 4 | a0002c0004t0001g0012 a0002c0004t0001g0082 a0002c0004t0001g0110 others(1): Show |
5 | HG00280.hp2 HG00738.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.690+818G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855688 | |||||||
chr9:21855966 | T | C | 1 | a0002c0002t0002g0093 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.690+1096T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21855966 | |||||||
chr9:21856280 | T | G | 4 | a0001c0003t0001g0004 a0001c0003t0001g0046 a0001c0003t0001g0049 others(1): Show |
6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.690+1410T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856280 | |||||||
chr9:21856471 | A | C | 112 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(109): Show |
124 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.690+1601A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856471 | |||||||
chr9:21856573 | T | G | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.690+1703T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856573 | |||||||
chr9:21856662 | G | C | 97 | a0001c0001t0001g0219 a0001c0001t0001g0270 a0001c0001t0001g0271 others(94): Show |
109 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.690+1792G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856662 | |||||||
chr9:21856677 | T | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0053 a0002c0002t0002g0054 |
4 | NA18612.hp2 NA18949.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+1807T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856677 | |||||||
chr9:21856686 | A | G | 50 | a0001c0001t0001g0158 a0001c0001t0003g0002 a0001c0001t0003g0005 others(47): Show |
59 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.690+1816A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856686 | |||||||
chr9:21856778 | C | T | 49 | a0001c0001t0001g0158 a0001c0001t0003g0002 a0001c0001t0003g0005 others(46): Show |
58 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.690+1908C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856778 | |||||||
chr9:21856877 | T | G | 1 | a0001c0001t0003g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.690+2007T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856877 | |||||||
chr9:21856891 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.690+2021C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21856891 | |||||||
chr9:21857245 | A | G | 180 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0219 others(177): Show |
205 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.691-2058A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857245 | |||||||
chr9:21857303 | G | A | 3 | a0002c0002t0001g0088 a0002c0002t0001g0105 a0002c0002t0037g0089 |
3 | HG02559.hp2 HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.691-2000G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857303 | |||||||
chr9:21857304 | C | T | 97 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0016 others(94): Show |
112 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.691-1999C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857304 | |||||||
chr9:21857370 | T | G | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.691-1933T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857370 | |||||||
chr9:21857449 | A | T | 4 | a0001c0003t0001g0004 a0001c0003t0001g0046 a0001c0003t0001g0049 others(1): Show |
6 | NA18939.hp2 NA18962.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1854A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857449 | |||||||
chr9:21857470 | T | C | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1833T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857470 | |||||||
chr9:21857715 | C | T | 1 | a0002c0002t0002g0064 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.691-1588C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857715 | |||||||
chr9:21857739 | T | G | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1564T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857739 | |||||||
chr9:21857777 | C | T | 1 | a0002c0002t0037g0089 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.691-1526C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857777 | |||||||
chr9:21857856 | A | G | 1 | a0001c0003t0001g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.691-1447A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857856 | |||||||
chr9:21857941 | G | A | 1 | a0001c0001t0003g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.691-1362G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21857941 | |||||||
chr9:21858041 | T | C | 6 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0031g0148 others(3): Show |
6 | HG01123.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.691-1262T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858041 | |||||||
chr9:21858124 | T | C | 4 | a0001c0001t0012g0130 a0001c0001t0012g0166 a0002c0002t0012g0315 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-1179T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858124 | |||||||
chr9:21858174 | T | A | 1 | a0001c0003t0001g0046 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.691-1129T>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858174 | |||||||
chr9:21858225 | G | A | 7 | a0001c0001t0009g0152 a0001c0001t0009g0201 a0001c0001t0031g0148 others(4): Show |
7 | HG01123.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.691-1078G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858225 | |||||||
chr9:21858251 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.691-1052C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858251 | |||||||
chr9:21858277 | T | C | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-1026T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858277 | |||||||
chr9:21858308 | A | G | 11 | a0001c0001t0004g0184 a0001c0001t0004g0185 a0002c0002t0004g0066 others(8): Show |
11 | HG01192.hp2 HG02055.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.691-995A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858308 | |||||||
chr9:21858320 | A | G | 1 | a0001c0001t0024g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.691-983A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858320 | |||||||
chr9:21858380 | A | G | 5 | a0001c0001t0008g0132 a0001c0001t0008g0133 a0001c0001t0008g0134 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-923A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858380 | |||||||
chr9:21858393 | G | C | 42 | a0001c0001t0003g0016 a0001c0001t0003g0212 a0001c0001t0003g0221 others(39): Show |
48 | HG01192.hp2 HG01433.hp1 HG01516.hp2 others(45): Show |
intron_variant | MODIFIER | c.691-910G>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858393 | |||||||
chr9:21858421 | G | A | 2 | a0001c0006t0001g0216 a0001c0006t0001g0218 |
2 | NA18999.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.691-882G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858421 | |||||||
chr9:21858451 | A | G | 79 | a0001c0001t0001g0219 a0001c0001t0002g0020 a0001c0001t0002g0028 others(76): Show |
90 | HG00438.hp2 HG00609.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.691-852A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858451 | |||||||
chr9:21858493 | C | T | 4 | a0001c0001t0010g0035 a0001c0001t0010g0257 a0001c0001t0010g0326 others(1): Show |
5 | NA18612.hp1 NA18948.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-810C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858493 | |||||||
chr9:21858650 | A | G | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-653A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858650 | |||||||
chr9:21858716 | C | G | 103 | a0001c0001t0001g0141 a0001c0001t0001g0198 a0001c0001t0003g0002 others(100): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.691-587C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858716 | |||||||
chr9:21858720 | A | G | 1 | a0001c0001t0024g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.691-583A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858720 | |||||||
chr9:21858830 | G | A | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.691-473G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21858830 | |||||||
chr9:21859056 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.691-247G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859056 | |||||||
chr9:21859195 | G | T | 43 | a0001c0001t0003g0016 a0001c0001t0003g0212 a0001c0001t0003g0221 others(40): Show |
49 | HG01192.hp2 HG01433.hp1 HG01516.hp2 others(46): Show |
intron_variant | MODIFIER | c.691-108G>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859195 | |||||||
chr9:21859196 | G | A | 1 | a0001c0003t0001g0041 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.691-107G>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 6/7 | chr9 | 21859196 | |||||||
chr9:21859663 | A | T | 2 | a0002c0002t0004g0066 a0002c0002t0004g0067 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.813+238A>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859663 | |||||||
chr9:21859665 | C | T | 1 | a0001c0001t0015g0164 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.813+240C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859665 | |||||||
chr9:21859790 | A | C | 1 | a0001c0001t0010g0257 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.813+365A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859790 | |||||||
chr9:21859836 | A | G | 2 | a0002c0002t0032g0068 a0002c0002t0033g0070 |
2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.813+411A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21859836 | |||||||
chr9:21859845 | GA | G | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.813+424delA | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21859845 | ||||||
chr9:21860064 | C | T | 1 | a0002c0004t0001g0082 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.813+639C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860064 | |||||||
chr9:21860327 | A | C | 5 | a0001c0001t0009g0152 a0001c0001t0031g0148 a0001c0010t0009g0057 others(2): Show |
5 | HG01123.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+902A>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860327 | |||||||
chr9:21860429 | C | T | 5 | a0001c0001t0020g0149 a0001c0001t0020g0199 a0001c0001t0034g0182 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+1004C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860429 | |||||||
chr9:21860732 | AGTTT | A | 5 | a0001c0001t0020g0149 a0001c0001t0020g0199 a0001c0001t0034g0182 others(2): Show |
5 | HG02559.hp1 HG02922.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-1235_814-1232d others(6): Show |
MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21860732 | ||||||
chr9:21860773 | C | T | 2 | a0002c0002t0001g0090 a0002c0002t0001g0099 |
2 | HG00639.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.814-1203C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860773 | |||||||
chr9:21860825 | C | G | 25 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(22): Show |
27 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.814-1151C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860825 | |||||||
chr9:21860981 | C | A | 2 | a0001c0001t0024g0190 a0001c0001t0024g0197 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-995C>A | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21860981 | |||||||
chr9:21861034 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.814-942T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861034 | |||||||
chr9:21861043 | T | G | 1 | a0002c0002t0012g0315 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.814-933T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861043 | |||||||
chr9:21861198 | A | G | 2 | a0001c0001t0024g0190 a0001c0001t0024g0197 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-778A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861198 | |||||||
chr9:21861319 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0242 |
2 | NA18966.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.814-657A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861319 | |||||||
chr9:21861412 | T | G | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.814-564T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861412 | |||||||
chr9:21861450 | C | G | 15 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(12): Show |
17 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.814-526C>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861450 | |||||||
chr9:21861470 | T | G | 2 | a0002c0002t0032g0068 a0002c0002t0033g0070 |
2 | HG03041.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.814-506T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861470 | |||||||
chr9:21861471 | C | T | 1 | a0002c0002t0004g0300 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.814-505C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861471 | |||||||
chr9:21861553 | C | T | 20 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(17): Show |
22 | HG00597.hp1 HG00609.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.814-423C>T | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861553 | |||||||
chr9:21861558 | A | G | 4 | a0001c0001t0009g0201 a0001c0001t0023g0058 a0001c0001t0023g0147 others(1): Show |
4 | HG02055.hp2 HG03516.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-418A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861558 | |||||||
chr9:21861613 | T | C | 1 | a0001c0001t0006g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.814-363T>C | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861613 | |||||||
chr9:21861634 | A | G | 1 | a0002c0004t0001g0082 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.814-342A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861634 | |||||||
chr9:21861861 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.814-115A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861861 | |||||||
chr9:21861878 | A | G | 2 | a0001c0001t0024g0190 a0001c0001t0024g0197 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.814-98A>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861878 | |||||||
chr9:21861903 | GT | G | 28 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0233 others(25): Show |
30 | HG00597.hp1 HG00609.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.814-62delT | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr9 | 21861903 | ||||||
chr9:21861904 | T | G | 45 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0017 others(42): Show |
54 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.814-72T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861904 | |||||||
chr9:21861905 | T | G | 1 | a0001c0001t0050g0170 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.814-71T>G | MTAP | ENSG00000099810.21 | transcript | ENST00000644715.2 | protein_coding | 7/7 | chr9 | 21861905 |