Item | Value |
---|---|
geneid | 4090 |
ensemblid | ENSG00000113658.18 |
hgncid | 6771 |
symbol | SMAD5 |
name | SMAD family member 5 |
refseq_nuc | NM_005903.7 |
refseq_prot | NP_005894.3 |
ensembl_nuc | ENST00000545279.6 |
ensembl_prot | ENSP00000441954.2 |
mane_status | MANE Select |
chr | chr5 |
start | 136132845 |
end | 136182733 |
strand | + |
ver | v1.2 |
region | chr5:136132845-136182733 |
region5000 | chr5:136127845-136187733 |
regionname0 | SMAD5_chr5_136132845_136182733 |
regionname5000 | SMAD5_chr5_136127845_136187733 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1395 | 291 | 80 | 43 | 132 | 14 | 20 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATGAC others(1390): Show |
chr5 | 136127845 | 136187733 | ||
a0001c0002 | 0/0 | 1395 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATGAC others(1390): Show |
chr5 | 136127845 | 136187733 | ||
a0001c0003 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATGAC others(1390): Show |
chr5 | 136127845 | 136187733 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7013 | 115 | 19 | 16 | 61 | 5 | 12 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0002 | 0/0 | 7017 | 60 | 10 | 5 | 36 | 4 | 5 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0003 | 0/0 | 7016 | 43 | 14 | 12 | 12 | 2 | 3 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0004 | 0/0 | 7016 | 8 | 6 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0005 | 0/0 | 7017 | 7 | 5 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0006 | 0/0 | 7017 | 7 | 0 | 0 | 7 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0007 | 0/0 | 7016 | 6 | 6 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0008 | 0/0 | 7013 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0009 | 0/0 | 7013 | 3 | 0 | 2 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0010 | 0/0 | 7013 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0011 | 0/0 | 7018 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7013): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0012 | 0/0 | 7012 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7007): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0013 | 0/0 | 7016 | 3 | 3 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0014 | 0/0 | 7014 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7009): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0015 | 0/0 | 7016 | 3 | 2 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0016 | 0/0 | 7014 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7009): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0017 | 0/0 | 7016 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0018 | 0/0 | 7016 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0019 | 0/0 | 7013 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0020 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0021 | 0/0 | 7013 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0022 | 0/0 | 7013 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0023 | 0/0 | 7013 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0024 | 0/0 | 7013 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0025 | 0/0 | 7017 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0026 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0027 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0028 | 0/0 | 7017 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0029 | 0/0 | 7014 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7009): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0030 | 0/0 | 7016 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7011): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0031 | 0/0 | 7017 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7012): Show |
chr5 | 136127845 | 136187733 |
a0001c0001t0032 | 0/0 | 7014 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7009): Show |
chr5 | 136127845 | 136187733 |
a0001c0002t0001 | 0/0 | 7013 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
a0001c0003t0009 | 0/0 | 7013 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | ATCCG others(7008): Show |
chr5 | 136127845 | 136187733 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 7 | 0 | 1 | 4 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0007g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0010g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0011g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0013g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0014g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0015g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0015g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0016g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0017g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0017g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0018g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0019g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0021g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0022g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0023g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0024g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0025g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0026g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0027g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0028g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0029g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0030g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0031g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0001t0032g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
a0001c0003t0009g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0114 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0058 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0093 | EUR | GBR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | FIN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00323 | hp2 | a0001 | c0001 | t0009 | g0146 | EUR | FIN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0204 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00423 | hp2 | a0001 | c0001 | t0020 | g0117 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0205 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00609 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00735 | hp2 | a0001 | c0001 | t0023 | g0207 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0133 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0127 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0076 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0152 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01258 | hp1 | a0001 | c0001 | t0009 | g0031 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01496 | hp2 | a0001 | c0001 | t0014 | g0130 | AMR | CLM | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01516 | hp1 | a0001 | c0001 | t0018 | g0015 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01517 | hp1 | a0001 | c0001 | t0018 | g0015 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01884 | hp1 | a0001 | c0001 | t0010 | g0182 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01934 | hp1 | a0001 | c0003 | t0009 | g0147 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02040 | hp2 | a0001 | c0001 | t0027 | g0115 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02129 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02165 | hp1 | a0001 | c0001 | t0028 | g0063 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CDX | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0041 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02451 | hp2 | a0001 | c0001 | t0029 | g0062 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0072 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0068 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02895 | hp2 | a0001 | c0001 | t0016 | g0078 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02897 | hp1 | a0001 | c0001 | t0016 | g0077 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02970 | hp2 | a0001 | c0001 | t0024 | g0202 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0022 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03195 | hp1 | a0001 | c0001 | t0031 | g0107 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03209 | hp1 | a0001 | c0001 | t0013 | g0064 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03225 | hp1 | a0001 | c0001 | t0013 | g0075 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03516 | hp1 | a0001 | c0001 | t0032 | g0071 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0003 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0131 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | YRI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | YRI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18939 | hp2 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18961 | hp1 | a0001 | c0001 | t0026 | g0005 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0206 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0116 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18979 | hp2 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18988 | hp1 | a0001 | c0001 | t0021 | g0157 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19030 | hp2 | a0001 | c0001 | t0025 | g0008 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19056 | hp1 | a0001 | c0001 | t0012 | g0037 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19068 | hp2 | a0001 | c0001 | t0012 | g0038 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19070 | hp2 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | ASW | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0046 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0069 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0151 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG03471 | hp2 | a0001 | c0001 | t0017 | g0070 | AFR | MSL | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA21309 | hp1 | a0001 | c0001 | t0022 | g0227 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0217 | REF | REF | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | SMAD5_chr5_136127845_136187733 | SMAD5 | chr5 | 136127845 | 136187733 |
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 |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136154066 | T | C | 1 | a0001c0002 | 2 | HG01168.hp1 HG01169.hp1 |
synonymous_variant | LOW | c.306T>C | p.His102His | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/8 | 668/7013 | 306/1398 | 102/465 | chr5 | 136154066 | |||
chr5:136174389 | C | T | 1 | a0001c0003 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1011C>T | p.Tyr337Tyr | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/8 | 1373/7013 | 1011/1398 | 337/465 | chr5 | 136174389 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136132914 | G | A | 1 | a0001c0001t0019 | 1 | HG00609.hp1 | 5_prime_UTR_variant | MODIFIER | c.-293G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/8 | 20847 | chr5 | 136132914 | ||||||
chr5:136147866 | G | A | 1 | a0001c0001t0020 | 1 | HG00423.hp2 | 5_prime_UTR_variant | MODIFIER | c.-210G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/8 | 5895 | chr5 | 136147866 | ||||||
chr5:136153746 | G | A | 2 | a0001c0001t0008 a0001c0001t0021 |
5 | HG00423.hp1 HG00438.hp2 NA18964.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/8 | 15 | chr5 | 136153746 | ||||||
chr5:136178162 | T | A | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 682 | chr5 | 136178162 | ||||||
chr5:136178234 | T | C | 1 | a0001c0001t0022 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*754T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 754 | chr5 | 136178234 | ||||||
chr5:136178367 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*887A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 887 | chr5 | 136178367 | ||||||
chr5:136178528 | A | G | 2 | a0001c0001t0003 a0001c0001t0032 |
44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1048A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1048 | chr5 | 136178528 | ||||||
chr5:136178653 | G | A | 2 | a0001c0001t0004 a0001c0001t0025 |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1173G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1173 | chr5 | 136178653 | ||||||
chr5:136178662 | T | C | 1 | a0001c0001t0005 | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1182T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1182 | chr5 | 136178662 | ||||||
chr5:136178801 | T | A | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1321 | chr5 | 136178801 | ||||||
chr5:136179045 | T | A | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1565T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1565 | chr5 | 136179045 | ||||||
chr5:136179054 | A | G | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1574A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1574 | chr5 | 136179054 | ||||||
chr5:136179114 | C | T | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1634C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1634 | chr5 | 136179114 | ||||||
chr5:136179190 | G | T | 1 | a0001c0001t0017 | 2 | HG02572.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1710G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1710 | chr5 | 136179190 | ||||||
chr5:136179268 | T | C | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1788T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1788 | chr5 | 136179268 | ||||||
chr5:136179440 | T | C | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1960 | chr5 | 136179440 | ||||||
chr5:136179468 | G | GA | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(5): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1998dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 1999 | INFO_REALIGN_3_PRIME | chr5 | 136179468 | |||||
chr5:136179480 | C | T | 1 | a0001c0001t0024 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2000C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2000 | chr5 | 136179480 | ||||||
chr5:136179500 | T | G | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2020T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2020 | chr5 | 136179500 | ||||||
chr5:136179504 | A | G | 1 | a0001c0001t0031 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2024A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2024 | chr5 | 136179504 | ||||||
chr5:136179651 | CCTTAA | C | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2172_*2176delCTTA others(1): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2172 | chr5 | 136179651 | ||||||
chr5:136179670 | A | G | 1 | a0001c0001t0021 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2190A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2190 | chr5 | 136179670 | ||||||
chr5:136179808 | G | GA | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2335 | INFO_REALIGN_3_PRIME | chr5 | 136179808 | |||||
chr5:136179823 | A | G | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2343A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2343 | chr5 | 136179823 | ||||||
chr5:136180020 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*2540A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2540 | chr5 | 136180020 | ||||||
chr5:136180050 | T | C | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2570T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2570 | chr5 | 136180050 | ||||||
chr5:136180268 | T | C | 2 | a0001c0001t0009 a0001c0003t0009 |
4 | HG00323.hp2 HG01071.hp1 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2788T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2788 | chr5 | 136180268 | ||||||
chr5:136180287 | T | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2807T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 2807 | chr5 | 136180287 | ||||||
chr5:136180500 | T | G | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*3020T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3020 | chr5 | 136180500 | ||||||
chr5:136180515 | T | C | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3035T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3035 | chr5 | 136180515 | ||||||
chr5:136180594 | G | A | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3114G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3114 | chr5 | 136180594 | ||||||
chr5:136180798 | G | T | 3 | a0001c0001t0006 a0001c0001t0020 a0001c0001t0028 |
9 | HG00423.hp2 HG02083.hp1 HG02129.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3318G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3318 | chr5 | 136180798 | ||||||
chr5:136181019 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3539A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3539 | chr5 | 136181019 | ||||||
chr5:136181047 | A | G | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3567A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3567 | chr5 | 136181047 | ||||||
chr5:136181069 | A | C | 1 | a0001c0001t0027 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3589A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3589 | chr5 | 136181069 | ||||||
chr5:136181148 | T | C | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3668T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3668 | chr5 | 136181148 | ||||||
chr5:136181231 | A | G | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3751A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3751 | chr5 | 136181231 | ||||||
chr5:136181462 | T | C | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*3982T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 3982 | chr5 | 136181462 | ||||||
chr5:136181519 | C | T | 1 | a0001c0001t0012 | 3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4039C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4039 | chr5 | 136181519 | ||||||
chr5:136181544 | C | T | 1 | a0001c0001t0010 | 3 | HG01243.hp1 HG01884.hp1 HG02486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4064C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4064 | chr5 | 136181544 | ||||||
chr5:136181717 | G | C | 1 | a0001c0001t0029 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4237G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4237 | chr5 | 136181717 | ||||||
chr5:136181857 | A | T | 1 | a0001c0001t0015 | 3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4377A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4377 | chr5 | 136181857 | ||||||
chr5:136182052 | T | G | 8 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(5): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*4572T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4572 | chr5 | 136182052 | ||||||
chr5:136182123 | G | A | 1 | a0001c0001t0018 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4643G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4643 | chr5 | 136182123 | ||||||
chr5:136182140 | C | T | 1 | a0001c0001t0023 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4660C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4660 | chr5 | 136182140 | ||||||
chr5:136182169 | A | G | 1 | a0001c0001t0028 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4689A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4689 | chr5 | 136182169 | ||||||
chr5:136182233 | G | GAA | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(12): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*4766_*4767dupAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4768 | INFO_REALIGN_3_PRIME | chr5 | 136182233 | |||||
chr5:136182233 | G | GAAA | 4 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(1): Show |
14 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4765_*4767dupAAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4768 | INFO_REALIGN_3_PRIME | chr5 | 136182233 | |||||
chr5:136182276 | T | A | 1 | a0001c0001t0018 | 2 | HG01516.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4796T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 4796 | chr5 | 136182276 | ||||||
chr5:136182481 | G | T | 1 | a0001c0001t0030 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5001G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5001 | chr5 | 136182481 | ||||||
chr5:136182519 | C | G | 1 | a0001c0001t0026 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5039C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5039 | chr5 | 136182519 | ||||||
chr5:136182554 | G | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*5074G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5074 | chr5 | 136182554 | ||||||
chr5:136182592 | A | G | 1 | a0001c0001t0005 | 7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5112A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 8/8 | 5112 | chr5 | 136182592 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:136133001 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+39T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133001 | |||||||
chr5:136133092 | G | T | 1 | a0001c0001t0003g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-245+130G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133092 | |||||||
chr5:136133174 | T | A | 1 | a0001c0001t0002g0034 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-245+212T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133174 | |||||||
chr5:136133177 | C | G | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+215C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133177 | |||||||
chr5:136133404 | C | T | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+442C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133404 | |||||||
chr5:136133435 | G | A | 1 | a0001c0001t0009g0133 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-245+473G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133435 | |||||||
chr5:136133811 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(56): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-245+849C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133811 | |||||||
chr5:136133831 | A | G | 1 | a0001c0001t0002g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-245+869A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133831 | |||||||
chr5:136133838 | T | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+876T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136133838 | |||||||
chr5:136134037 | T | TG | 20 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(17): Show |
28 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-245+1091dupG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | ||||||
chr5:136134037 | TG | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0031 others(27): Show |
40 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-245+1091delG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | ||||||
chr5:136134037 | TGG | T | 28 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(25): Show |
29 | HG00099.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.-245+1090_-245+109 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | ||||||
chr5:136134037 | TGGG | T | 121 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0005 others(118): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-245+1089_-245+109 others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136134037 | ||||||
chr5:136134042 | G | C | 3 | a0001c0001t0001g0134 a0001c0001t0016g0077 a0001c0001t0016g0078 |
3 | HG02895.hp2 HG02897.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-245+1080G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134042 | |||||||
chr5:136134043 | G | C | 5 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
5 | NA18947.hp1 NA18952.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.-245+1081G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134043 | |||||||
chr5:136134048 | G | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+1086G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134048 | |||||||
chr5:136134050 | G | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-245+1088G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134050 | |||||||
chr5:136134081 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1119T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134081 | |||||||
chr5:136134255 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-245+1293G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134255 | |||||||
chr5:136134352 | T | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1390T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134352 | |||||||
chr5:136134447 | A | T | 1 | a0001c0001t0002g0123 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-245+1485A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134447 | |||||||
chr5:136134493 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1531T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134493 | |||||||
chr5:136134576 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-245+1614A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134576 | |||||||
chr5:136134654 | A | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0076 |
3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-245+1692A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134654 | |||||||
chr5:136134813 | T | C | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-245+1851T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134813 | |||||||
chr5:136134855 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+1893T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136134855 | |||||||
chr5:136135086 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-245+2124G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135086 | |||||||
chr5:136135128 | C | A | 1 | a0001c0001t0003g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-245+2166C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135128 | |||||||
chr5:136135345 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2383T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135345 | |||||||
chr5:136135394 | A | G | 1 | a0001c0001t0013g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-245+2432A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135394 | |||||||
chr5:136135411 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-245+2449G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135411 | |||||||
chr5:136135597 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-245+2635C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135597 | |||||||
chr5:136135823 | C | T | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2861C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135823 | |||||||
chr5:136135833 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-245+2871A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135833 | |||||||
chr5:136135950 | C | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+2988C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135950 | |||||||
chr5:136135962 | G | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3000G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136135962 | |||||||
chr5:136136122 | A | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3160A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136122 | |||||||
chr5:136136204 | T | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3242T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136204 | |||||||
chr5:136136239 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+3277G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136239 | |||||||
chr5:136136285 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+3323C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136285 | |||||||
chr5:136136367 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-245+3405G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136367 | |||||||
chr5:136136384 | G | T | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+3422G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136384 | |||||||
chr5:136136438 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-245+3476T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136438 | |||||||
chr5:136136505 | G | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3543G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136505 | |||||||
chr5:136136563 | A | C | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+3601A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136563 | |||||||
chr5:136136691 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-245+3729A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136691 | |||||||
chr5:136136726 | T | C | 1 | a0001c0001t0021g0157 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-245+3764T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136726 | |||||||
chr5:136136735 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0074 |
3 | HG03041.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-245+3773C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136735 | |||||||
chr5:136136754 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0212 |
2 | HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-245+3792T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136754 | |||||||
chr5:136136759 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-245+3797C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136759 | |||||||
chr5:136136849 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-245+3887C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136849 | |||||||
chr5:136136898 | C | T | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+3936C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136136898 | |||||||
chr5:136137016 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0076 |
3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-245+4054G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137016 | |||||||
chr5:136137017 | A | AT | 14 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(11): Show |
14 | HG00621.hp1 HG00642.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-245+4075dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | ||||||
chr5:136137017 | AT | A | 16 | a0001c0001t0001g0158 a0001c0001t0002g0034 a0001c0001t0002g0118 others(13): Show |
17 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-245+4075delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | ||||||
chr5:136137017 | ATT | A | 109 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(106): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-245+4074_-245+407 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137017 | ||||||
chr5:136137040 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+4078C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137040 | |||||||
chr5:136137057 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-245+4095G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137057 | |||||||
chr5:136137059 | T | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+4097T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137059 | |||||||
chr5:136137161 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-245+4199C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137161 | |||||||
chr5:136137188 | A | G | 1 | a0001c0001t0023g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-245+4226A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137188 | |||||||
chr5:136137257 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+4295T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137257 | |||||||
chr5:136137258 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0081 |
4 | NA18953.hp2 NA19065.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-245+4296G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137258 | |||||||
chr5:136137270 | A | ACCCC | 39 | a0001c0001t0002g0006 a0001c0001t0002g0025 a0001c0001t0002g0026 others(36): Show |
48 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.-245+4314_-245+431 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | ||||||
chr5:136137270 | A | ACCCCC | 53 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0011 others(50): Show |
72 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-245+4313_-245+431 others(9): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | ||||||
chr5:136137270 | A | ACCCCCC | 20 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0002g0084 others(17): Show |
22 | HG00597.hp2 HG01255.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-245+4312_-245+431 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136137270 | ||||||
chr5:136137284 | C | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+4322C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137284 | |||||||
chr5:136137292 | A | G | 1 | a0001c0001t0004g0044 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-245+4330A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137292 | |||||||
chr5:136137306 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-245+4344C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137306 | |||||||
chr5:136137426 | A | G | 2 | a0001c0001t0006g0111 a0001c0001t0018g0015 |
3 | HG01516.hp1 HG01517.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-245+4464A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137426 | |||||||
chr5:136137491 | C | T | 58 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(55): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-245+4529C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137491 | |||||||
chr5:136137799 | A | C | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-245+4837A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137799 | |||||||
chr5:136137941 | C | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0089 a0001c0001t0002g0110 |
4 | HG01099.hp1 HG01168.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-245+4979C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136137941 | |||||||
chr5:136138003 | A | G | 1 | a0001c0001t0008g0206 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-245+5041A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138003 | |||||||
chr5:136138073 | G | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0016 others(29): Show |
44 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.-245+5111G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138073 | |||||||
chr5:136138099 | T | A | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-245+5137T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138099 | |||||||
chr5:136138136 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+5174T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138136 | |||||||
chr5:136138406 | C | T | 1 | a0001c0001t0001g0033 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.-245+5444C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138406 | |||||||
chr5:136138521 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-245+5559C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138521 | |||||||
chr5:136138615 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-245+5653A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138615 | |||||||
chr5:136138673 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-245+5711C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138673 | |||||||
chr5:136138757 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-245+5795A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138757 | |||||||
chr5:136138786 | C | A | 1 | a0001c0001t0002g0092 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-245+5824C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138786 | |||||||
chr5:136138811 | A | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+5849A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138811 | |||||||
chr5:136138837 | G | C | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+5875G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138837 | |||||||
chr5:136138980 | G | A | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-245+6018G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136138980 | |||||||
chr5:136139125 | GCT | G | 10 | a0001c0001t0003g0019 a0001c0001t0003g0035 a0001c0001t0003g0053 others(7): Show |
11 | HG01099.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-245+6166_-245+616 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139125 | ||||||
chr5:136139126 | C | CTG | 68 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(65): Show |
87 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | ||||||
chr5:136139126 | C | CTGTG | 15 | a0001c0001t0002g0010 a0001c0001t0002g0027 a0001c0001t0002g0034 others(12): Show |
16 | HG01928.hp1 HG01993.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | ||||||
chr5:136139126 | C | CTGTGTG | 3 | a0001c0001t0013g0064 a0001c0001t0017g0070 a0001c0001t0017g0072 |
3 | HG02572.hp1 HG03209.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-245+6165_-245+616 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | ||||||
chr5:136139126 | CTCTG | C | 5 | a0001c0001t0002g0093 a0001c0001t0002g0094 a0001c0001t0012g0036 others(2): Show |
5 | HG00140.hp2 NA18979.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.-245+6166_-245+616 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | ||||||
chr5:136139126 | CTCTGTG | C | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-245+6166_-245+617 others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139126 | ||||||
chr5:136139128 | C | CTG | 13 | a0001c0001t0001g0150 a0001c0001t0001g0178 a0001c0001t0001g0179 others(10): Show |
13 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(10): Show |
intron_variant | MODIFIER | c.-245+6196_-245+619 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139128 | ||||||
chr5:136139128 | C | CTGTG | 3 | a0001c0001t0010g0151 a0001c0001t0010g0152 a0001c0001t0010g0182 |
3 | HG01243.hp1 HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-245+6194_-245+619 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136139128 | ||||||
chr5:136139128 | C | G | 108 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(105): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.-245+6166C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139128 | |||||||
chr5:136139140 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0213 |
2 | NA18990.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-245+6178G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139140 | |||||||
chr5:136139234 | T | C | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-245+6272T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139234 | |||||||
chr5:136139275 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-245+6313A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139275 | |||||||
chr5:136139280 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0222 |
2 | HG01952.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-245+6318A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139280 | |||||||
chr5:136139441 | A | C | 1 | a0001c0001t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-245+6479A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139441 | |||||||
chr5:136139450 | G | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-245+6488G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139450 | |||||||
chr5:136139568 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-245+6606T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139568 | |||||||
chr5:136139590 | C | T | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-245+6628C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139590 | |||||||
chr5:136139718 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0014g0068 |
2 | HG00597.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-245+6756C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139718 | |||||||
chr5:136139827 | A | C | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-245+6865A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139827 | |||||||
chr5:136139827 | A | G | 125 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(122): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-245+6865A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139827 | |||||||
chr5:136139937 | C | T | 5 | a0001c0001t0004g0008 a0001c0001t0004g0042 a0001c0001t0004g0043 others(2): Show |
6 | HG01258.hp2 HG01346.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-245+6975C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136139937 | |||||||
chr5:136140023 | C | CT | 7 | a0001c0001t0001g0149 a0001c0001t0002g0091 a0001c0001t0007g0003 others(4): Show |
11 | HG02615.hp2 HG02809.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-245+7078dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136140023 | ||||||
chr5:136140023 | CT | C | 6 | a0001c0001t0001g0214 a0001c0001t0002g0112 a0001c0001t0013g0075 others(3): Show |
6 | HG01496.hp2 HG01993.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-245+7078delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136140023 | ||||||
chr5:136140228 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0121 |
4 | NA18941.hp2 NA18945.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-245+7266C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136140228 | |||||||
chr5:136141075 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-6757T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141075 | |||||||
chr5:136141088 | T | C | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(111): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-244-6744T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141088 | |||||||
chr5:136141173 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-244-6659A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141173 | |||||||
chr5:136141179 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02083.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-244-6653T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141179 | |||||||
chr5:136141197 | A | T | 1 | a0001c0001t0002g0109 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-244-6635A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141197 | |||||||
chr5:136141254 | C | A | 1 | a0001c0001t0002g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-244-6578C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141254 | |||||||
chr5:136141494 | C | T | 2 | a0001c0001t0003g0052 a0001c0001t0003g0060 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-244-6338C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141494 | |||||||
chr5:136141604 | C | T | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-244-6228C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141604 | |||||||
chr5:136141702 | TAAAG | T | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-244-6127_-244-612 others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136141702 | ||||||
chr5:136141836 | C | A | 1 | a0001c0001t0004g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-244-5996C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141836 | |||||||
chr5:136141936 | G | C | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5896G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141936 | |||||||
chr5:136141937 | C | A | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5895C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141937 | |||||||
chr5:136141938 | A | G | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5894A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141938 | |||||||
chr5:136141940 | T | C | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5892T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141940 | |||||||
chr5:136141941 | TTA | T | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5890_-244-588 others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141941 | |||||||
chr5:136141944 | A | G | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-5888A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136141944 | |||||||
chr5:136142032 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-244-5800C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142032 | |||||||
chr5:136142276 | G | A | 3 | a0001c0001t0013g0064 a0001c0001t0013g0069 a0001c0001t0014g0068 |
3 | HG02486.hp1 HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-244-5556G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142276 | |||||||
chr5:136142621 | C | T | 1 | a0001c0001t0003g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-244-5211C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142621 | |||||||
chr5:136142843 | C | A | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | HG01099.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-244-4989C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142843 | |||||||
chr5:136142966 | G | T | 1 | a0001c0001t0003g0059 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-244-4866G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142966 | |||||||
chr5:136142972 | C | T | 1 | a0001c0001t0003g0018 | 2 | NA19081.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-244-4860C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136142972 | |||||||
chr5:136143035 | A | C | 2 | a0001c0001t0010g0152 a0001c0001t0010g0182 |
2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-244-4797A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143035 | |||||||
chr5:136143113 | A | G | 1 | a0001c0001t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-244-4719A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143113 | |||||||
chr5:136143198 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244-4634A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143198 | |||||||
chr5:136143266 | C | CT | 64 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(61): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-244-4552dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136143266 | ||||||
chr5:136143659 | A | C | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(111): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-244-4173A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143659 | |||||||
chr5:136143734 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG02698.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-244-4098T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143734 | |||||||
chr5:136143746 | C | G | 1 | a0001c0001t0002g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-244-4086C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136143746 | |||||||
chr5:136144055 | A | G | 2 | a0001c0001t0004g0008 a0001c0001t0025g0008 |
3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-244-3777A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144055 | |||||||
chr5:136144085 | C | T | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-3747C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144085 | |||||||
chr5:136144325 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0159 |
2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-244-3507G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144325 | |||||||
chr5:136144392 | AGCAAAAA others(18): Show |
A | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-244-3439_-244-341 others(29): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144392 | |||||||
chr5:136144429 | G | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-3403G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144429 | |||||||
chr5:136144721 | A | G | 1 | a0001c0001t0006g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-244-3111A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144721 | |||||||
chr5:136144753 | T | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0109 others(1): Show |
5 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-3079T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136144753 | |||||||
chr5:136145065 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-244-2767G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145065 | |||||||
chr5:136145116 | A | AT | 125 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(122): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-244-2706dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136145116 | ||||||
chr5:136145370 | C | A | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-244-2462C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145370 | |||||||
chr5:136145539 | TC | T | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-244-2292delC | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145539 | |||||||
chr5:136145672 | T | C | 58 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(55): Show |
73 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.-244-2160T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145672 | |||||||
chr5:136145983 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0160 |
2 | HG02559.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-244-1849T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136145983 | |||||||
chr5:136146001 | A | G | 4 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0109 others(1): Show |
5 | HG02559.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-244-1831A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146001 | |||||||
chr5:136146018 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-244-1814G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146018 | |||||||
chr5:136146457 | G | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-1375G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146457 | |||||||
chr5:136146508 | T | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-1324T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146508 | |||||||
chr5:136146527 | T | G | 1 | a0001c0001t0013g0075 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-244-1305T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146527 | |||||||
chr5:136146580 | G | T | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-244-1252G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146580 | |||||||
chr5:136146681 | G | C | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-244-1151G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146681 | |||||||
chr5:136146846 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-244-986G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146846 | |||||||
chr5:136146896 | C | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-244-936C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136146896 | |||||||
chr5:136147138 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-244-694G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147138 | |||||||
chr5:136147324 | G | A | 40 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0016 others(37): Show |
53 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-244-508G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147324 | |||||||
chr5:136147332 | G | T | 120 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-244-500G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147332 | |||||||
chr5:136147645 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-244-187A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147645 | |||||||
chr5:136147691 | A | G | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-244-141A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147691 | |||||||
chr5:136147819 | A | AT | 106 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(103): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
splice_acceptor_variant&intron_variant | HIGH | c.-244-3dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 136147819 | ||||||
chr5:136147819 | A | T | 9 | a0001c0001t0003g0074 a0001c0001t0004g0008 a0001c0001t0004g0039 others(6): Show |
10 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-244-13A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 1/7 | chr5 | 136147819 | |||||||
chr5:136148163 | T | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-170+257T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148163 | |||||||
chr5:136148200 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+294A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148200 | |||||||
chr5:136148254 | G | GT | 121 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(118): Show |
156 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-170+350dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136148254 | ||||||
chr5:136148257 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+351C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148257 | |||||||
chr5:136148323 | T | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+417T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148323 | |||||||
chr5:136148324 | G | T | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-170+418G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148324 | |||||||
chr5:136148363 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-170+457T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148363 | |||||||
chr5:136148459 | T | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0190 a0001c0001t0001g0194 others(4): Show |
7 | HG00099.hp1 HG00642.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170+553T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148459 | |||||||
chr5:136148500 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+594C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148500 | |||||||
chr5:136148830 | C | T | 1 | a0001c0001t0014g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-170+924C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148830 | |||||||
chr5:136148832 | C | T | 1 | a0001c0001t0022g0227 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-170+926C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148832 | |||||||
chr5:136148874 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+968A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148874 | |||||||
chr5:136148909 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-170+1003A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136148909 | |||||||
chr5:136149139 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+1233A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149139 | |||||||
chr5:136149247 | G | C | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+1341G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149247 | |||||||
chr5:136149288 | T | C | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-170+1382T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149288 | |||||||
chr5:136149298 | T | C | 2 | a0001c0001t0013g0064 a0001c0001t0014g0068 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-170+1392T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149298 | |||||||
chr5:136149332 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-170+1426T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149332 | |||||||
chr5:136149337 | C | T | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-170+1431C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149337 | |||||||
chr5:136149433 | A | G | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-170+1527A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149433 | |||||||
chr5:136149440 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+1534A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149440 | |||||||
chr5:136149482 | C | CT | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170+1590dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136149482 | ||||||
chr5:136149708 | C | T | 60 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(57): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.-170+1802C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149708 | |||||||
chr5:136149742 | C | A | 114 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(111): Show |
148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-170+1836C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149742 | |||||||
chr5:136149804 | A | C | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-170+1898A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149804 | |||||||
chr5:136149805 | G | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-170+1899G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149805 | |||||||
chr5:136149926 | A | G | 115 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(112): Show |
149 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-170+2020A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149926 | |||||||
chr5:136149984 | A | G | 1 | a0001c0001t0003g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-170+2078A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136149984 | |||||||
chr5:136150341 | G | A | 1 | a0001c0001t0004g0041 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-170+2435G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150341 | |||||||
chr5:136150441 | C | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-170+2535C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150441 | |||||||
chr5:136150519 | T | C | 46 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(43): Show |
60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-170+2613T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150519 | |||||||
chr5:136150631 | A | G | 2 | a0001c0001t0004g0008 a0001c0001t0025g0008 |
3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-170+2725A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150631 | |||||||
chr5:136150678 | A | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-170+2772A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150678 | |||||||
chr5:136150695 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0003g0045 |
2 | HG02738.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-170+2789G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150695 | |||||||
chr5:136150696 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-170+2790T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150696 | |||||||
chr5:136150847 | G | T | 122 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(119): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-169-2745G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150847 | |||||||
chr5:136150887 | T | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01928.hp2 HG01952.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169-2705T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136150887 | |||||||
chr5:136151050 | A | G | 9 | a0001c0001t0002g0034 a0001c0001t0002g0092 a0001c0001t0002g0096 others(6): Show |
9 | HG00140.hp1 HG00673.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-169-2542A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151050 | |||||||
chr5:136151153 | A | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01928.hp2 HG01952.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.-169-2439A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151153 | |||||||
chr5:136151175 | TG | T | 9 | a0001c0001t0003g0074 a0001c0001t0004g0008 a0001c0001t0004g0039 others(6): Show |
10 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169-2415delG | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 136151175 | ||||||
chr5:136151626 | G | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1966G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151626 | |||||||
chr5:136151691 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-169-1901C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151691 | |||||||
chr5:136151719 | A | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-169-1873A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151719 | |||||||
chr5:136151737 | A | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-1855A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151737 | |||||||
chr5:136151780 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1812A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151780 | |||||||
chr5:136151804 | A | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-1788A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151804 | |||||||
chr5:136151820 | G | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1772G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151820 | |||||||
chr5:136151854 | A | G | 1 | a0001c0001t0003g0050 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-169-1738A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151854 | |||||||
chr5:136151952 | G | T | 1 | a0001c0001t0003g0049 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-169-1640G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136151952 | |||||||
chr5:136152263 | G | T | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-169-1329G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152263 | |||||||
chr5:136152464 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.-169-1128A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152464 | |||||||
chr5:136152611 | G | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-981G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152611 | |||||||
chr5:136152707 | C | T | 8 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(5): Show |
10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-169-885C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152707 | |||||||
chr5:136152797 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0223 a0001c0001t0013g0075 |
3 | HG03130.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-169-795G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152797 | |||||||
chr5:136152876 | T | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0149 others(2): Show |
10 | NA18941.hp1 NA18964.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.-169-716T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136152876 | |||||||
chr5:136153041 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-169-551G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153041 | |||||||
chr5:136153215 | G | A | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-169-377G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153215 | |||||||
chr5:136153536 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-169-56A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 2/7 | chr5 | 136153536 | |||||||
chr5:136154202 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.403+39A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154202 | |||||||
chr5:136154384 | G | A | 1 | a0001c0001t0029g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.403+221G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154384 | |||||||
chr5:136154493 | A | G | 1 | a0001c0001t0002g0080 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.403+330A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154493 | |||||||
chr5:136154948 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.403+785G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154948 | |||||||
chr5:136154954 | CTT | C | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.403+793_403+794del others(2): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136154954 | ||||||
chr5:136154964 | G | A | 7 | a0001c0001t0001g0156 a0001c0001t0004g0008 a0001c0001t0004g0041 others(4): Show |
8 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+801G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136154964 | |||||||
chr5:136155046 | A | G | 1 | a0001c0001t0015g0076 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.403+883A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155046 | |||||||
chr5:136155127 | C | T | 1 | a0001c0001t0027g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.403+964C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155127 | |||||||
chr5:136155128 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.403+965A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155128 | |||||||
chr5:136155196 | G | A | 2 | a0001c0001t0003g0053 a0001c0001t0003g0054 |
2 | HG01099.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.403+1033G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155196 | |||||||
chr5:136155222 | A | G | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.403+1059A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155222 | |||||||
chr5:136155293 | T | C | 1 | a0001c0001t0012g0036 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.403+1130T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155293 | |||||||
chr5:136155457 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.403+1294G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155457 | |||||||
chr5:136155707 | C | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.403+1544C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155707 | |||||||
chr5:136155887 | T | G | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+1724T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136155887 | |||||||
chr5:136156276 | G | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.403+2113G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156276 | |||||||
chr5:136156355 | T | A | 1 | a0001c0001t0002g0087 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.403+2192T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156355 | |||||||
chr5:136156708 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+2545C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156708 | |||||||
chr5:136156824 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.403+2661C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156824 | |||||||
chr5:136156835 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0209 |
2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.403+2672C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156835 | |||||||
chr5:136156955 | A | AC | 42 | a0001c0001t0002g0023 a0001c0001t0003g0004 a0001c0001t0003g0009 others(39): Show |
56 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.403+2798dupC | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136156955 | ||||||
chr5:136156980 | C | T | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.403+2817C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136156980 | |||||||
chr5:136157512 | A | T | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.404-3344A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157512 | |||||||
chr5:136157615 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0076 |
3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404-3241G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157615 | |||||||
chr5:136157712 | G | A | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.404-3144G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157712 | |||||||
chr5:136157759 | C | T | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-3097C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157759 | |||||||
chr5:136157879 | G | A | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-2977G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157879 | |||||||
chr5:136157899 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.404-2957G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157899 | |||||||
chr5:136157900 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.404-2956G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136157900 | |||||||
chr5:136158171 | C | A | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.404-2685C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158171 | |||||||
chr5:136158223 | G | A | 1 | a0001c0002t0001g0029 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.404-2633G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158223 | |||||||
chr5:136158283 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.404-2573A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158283 | |||||||
chr5:136158332 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-2524A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158332 | |||||||
chr5:136158385 | T | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.404-2471T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158385 | |||||||
chr5:136158472 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0209 |
2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.404-2384C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158472 | |||||||
chr5:136158538 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.404-2318A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158538 | |||||||
chr5:136158548 | A | C | 1 | a0001c0001t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-2308A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158548 | |||||||
chr5:136158563 | G | C | 1 | a0001c0001t0005g0125 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.404-2293G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158563 | |||||||
chr5:136158656 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.404-2200T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158656 | |||||||
chr5:136158696 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.404-2160G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158696 | |||||||
chr5:136158823 | C | G | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-2033C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158823 | |||||||
chr5:136158823 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.404-2033C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158823 | |||||||
chr5:136158878 | G | A | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.404-1978G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158878 | |||||||
chr5:136158898 | C | CA | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(120): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.404-1947dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136158898 | ||||||
chr5:136158987 | G | A | 2 | a0001c0001t0015g0022 a0001c0001t0015g0076 |
3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.404-1869G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136158987 | |||||||
chr5:136159001 | T | C | 1 | a0001c0001t0003g0053 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.404-1855T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159001 | |||||||
chr5:136159049 | T | A | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-1807T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159049 | |||||||
chr5:136159167 | T | C | 1 | a0001c0001t0003g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.404-1689T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159167 | |||||||
chr5:136159179 | G | A | 2 | a0001c0001t0002g0092 a0001c0001t0002g0096 |
2 | HG00673.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.404-1677G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159179 | |||||||
chr5:136159336 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0158 |
3 | NA18956.hp2 NA19001.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.404-1520T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159336 | |||||||
chr5:136159489 | C | T | 1 | a0001c0001t0003g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.404-1367C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159489 | |||||||
chr5:136159505 | A | G | 1 | a0001c0001t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-1351A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159505 | |||||||
chr5:136159589 | T | A | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-1267T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159589 | |||||||
chr5:136159634 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.404-1222A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159634 | |||||||
chr5:136159645 | C | CT | 109 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(106): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.404-1210dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 136159645 | ||||||
chr5:136159768 | G | A | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.404-1088G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136159768 | |||||||
chr5:136160011 | T | G | 1 | a0001c0001t0004g0044 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.404-845T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160011 | |||||||
chr5:136160083 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.404-773C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160083 | |||||||
chr5:136160312 | T | A | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404-544T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160312 | |||||||
chr5:136160755 | G | A | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-101G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 3/7 | chr5 | 136160755 | |||||||
chr5:136161131 | C | CA | 119 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(116): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.655+37dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161131 | ||||||
chr5:136161131 | C | CAA | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+36_655+37dupAA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161131 | ||||||
chr5:136161145 | T | A | 1 | a0001c0001t0031g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.655+38T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161145 | |||||||
chr5:136161153 | A | C | 1 | a0001c0001t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.655+46A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161153 | |||||||
chr5:136161206 | TATA | T | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.655+103_655+105del others(3): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136161206 | ||||||
chr5:136161540 | G | C | 2 | a0001c0001t0004g0008 a0001c0001t0025g0008 |
3 | HG02451.hp1 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.655+433G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161540 | |||||||
chr5:136161582 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.655+475G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136161582 | |||||||
chr5:136162094 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.655+987C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162094 | |||||||
chr5:136162124 | A | G | 8 | a0001c0001t0002g0011 a0001c0001t0002g0025 a0001c0001t0002g0083 others(5): Show |
11 | HG00597.hp2 HG00621.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+1017A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162124 | |||||||
chr5:136162320 | G | A | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-952G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162320 | |||||||
chr5:136162487 | T | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-785T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162487 | |||||||
chr5:136162553 | A | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.656-719A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162553 | |||||||
chr5:136162630 | C | G | 1 | a0001c0001t0005g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.656-642C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162630 | |||||||
chr5:136162732 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.656-540C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162732 | |||||||
chr5:136162840 | G | A | 5 | a0001c0001t0004g0008 a0001c0001t0004g0042 a0001c0001t0004g0043 others(2): Show |
6 | HG01258.hp2 HG01346.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-432G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162840 | |||||||
chr5:136162851 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.656-421C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162851 | |||||||
chr5:136162861 | T | G | 1 | a0001c0001t0031g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.656-411T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136162861 | |||||||
chr5:136163011 | A | C | 1 | a0001c0001t0002g0085 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.656-261A>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163011 | |||||||
chr5:136163092 | A | G | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.656-180A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163092 | |||||||
chr5:136163156 | T | C | 4 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 others(1): Show |
5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-116T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | chr5 | 136163156 | |||||||
chr5:136163255 | AT | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.656-9delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr5 | 136163255 | ||||||
chr5:136163522 | T | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+131T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163522 | |||||||
chr5:136163607 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0060 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.775+216G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163607 | |||||||
chr5:136163711 | A | G | 1 | a0001c0001t0001g0229 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.775+320A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163711 | |||||||
chr5:136163884 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.775+493A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163884 | |||||||
chr5:136163960 | C | A | 2 | a0001c0001t0014g0130 a0001c0001t0014g0131 |
2 | HG01496.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.775+569C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136163960 | |||||||
chr5:136164132 | G | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+741G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164132 | |||||||
chr5:136164183 | G | A | 4 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 others(1): Show |
5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+792G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164183 | |||||||
chr5:136164232 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.775+841T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164232 | |||||||
chr5:136164314 | C | T | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.775+923C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164314 | |||||||
chr5:136164533 | T | A | 7 | a0001c0001t0002g0034 a0001c0001t0002g0092 a0001c0001t0002g0096 others(4): Show |
7 | HG00673.hp1 HG02040.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+1142T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164533 | |||||||
chr5:136164569 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.775+1178G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164569 | |||||||
chr5:136164707 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.775+1316G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164707 | |||||||
chr5:136164743 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.775+1352T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164743 | |||||||
chr5:136164858 | T | G | 5 | a0001c0001t0001g0144 a0001c0001t0001g0153 a0001c0001t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02572.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+1467T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136164858 | |||||||
chr5:136165373 | T | G | 3 | a0001c0001t0002g0106 a0001c0001t0015g0022 a0001c0001t0015g0076 |
4 | HG01167.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+1982T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165373 | |||||||
chr5:136165377 | G | T | 8 | a0001c0001t0002g0027 a0001c0001t0002g0082 a0001c0001t0002g0092 others(5): Show |
9 | HG00673.hp1 HG02040.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.775+1986G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165377 | |||||||
chr5:136165393 | T | G | 60 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(57): Show |
75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.775+2002T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165393 | |||||||
chr5:136165421 | T | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+2030T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165421 | |||||||
chr5:136165639 | C | T | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+2248C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165639 | |||||||
chr5:136165662 | A | AT | 6 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0148 others(3): Show |
6 | HG02056.hp2 HG02071.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+2308dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | AT | A | 34 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0134 others(31): Show |
35 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.775+2308delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(2): Show |
A | 5 | a0001c0001t0002g0084 a0001c0001t0007g0003 a0001c0001t0007g0067 others(2): Show |
9 | HG00423.hp2 HG02056.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2300_775+2308d others(11): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(3): Show |
A | 55 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(52): Show |
70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.775+2299_775+2308d others(12): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(4): Show |
A | 48 | a0001c0001t0002g0027 a0001c0001t0002g0034 a0001c0001t0002g0082 others(45): Show |
61 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.775+2298_775+2308d others(13): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(5): Show |
A | 9 | a0001c0001t0003g0055 a0001c0001t0003g0132 a0001c0001t0005g0028 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.775+2297_775+2308d others(14): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(6): Show |
A | 7 | a0001c0001t0001g0162 a0001c0001t0008g0188 a0001c0001t0013g0075 others(4): Show |
8 | HG01167.hp2 HG01496.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.775+2296_775+2308d others(15): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165662 | ATTTTTTT others(8): Show |
A | 5 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2294_775+2308d others(17): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136165662 | ||||||
chr5:136165663 | T | TA | 9 | a0001c0001t0001g0002 a0001c0001t0001g0186 a0001c0001t0001g0190 others(6): Show |
9 | HG01175.hp1 HG01952.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2272_775+2273i others(3): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165663 | |||||||
chr5:136165664 | T | A | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(23): Show |
35 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.775+2273T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165664 | |||||||
chr5:136165665 | T | A | 12 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0171 others(9): Show |
12 | HG01069.hp1 HG01884.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+2274T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165665 | |||||||
chr5:136165666 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.775+2275T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165666 | |||||||
chr5:136165670 | T | A | 1 | a0001c0001t0010g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.775+2279T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165670 | |||||||
chr5:136165672 | T | A | 1 | a0001c0001t0001g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.775+2281T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165672 | |||||||
chr5:136165673 | T | A | 5 | a0001c0001t0002g0084 a0001c0001t0007g0003 a0001c0001t0007g0067 others(2): Show |
9 | HG00423.hp2 HG02056.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+2282T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165673 | |||||||
chr5:136165674 | T | A | 55 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(52): Show |
70 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.775+2283T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165674 | |||||||
chr5:136165675 | T | A | 48 | a0001c0001t0002g0027 a0001c0001t0002g0034 a0001c0001t0002g0082 others(45): Show |
61 | HG00140.hp1 HG00639.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.775+2284T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165675 | |||||||
chr5:136165676 | T | A | 9 | a0001c0001t0003g0055 a0001c0001t0003g0132 a0001c0001t0005g0028 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.775+2285T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165676 | |||||||
chr5:136165677 | T | A | 6 | a0001c0001t0001g0162 a0001c0001t0013g0075 a0001c0001t0014g0130 others(3): Show |
7 | HG01167.hp2 HG01496.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+2286T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165677 | |||||||
chr5:136165679 | T | A | 5 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 others(2): Show |
5 | HG02895.hp2 HG02897.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.775+2288T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165679 | |||||||
chr5:136165890 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.775+2499G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165890 | |||||||
chr5:136165933 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.775+2542A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136165933 | |||||||
chr5:136166035 | T | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+2644T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166035 | |||||||
chr5:136166054 | A | T | 1 | a0001c0001t0005g0126 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.775+2663A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166054 | |||||||
chr5:136166155 | A | AT | 21 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0016 others(18): Show |
31 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.775+2772dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136166155 | ||||||
chr5:136166166 | C | CT | 11 | a0001c0001t0001g0228 a0001c0001t0003g0009 a0001c0001t0003g0016 others(8): Show |
14 | HG01993.hp1 HG02602.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.775+2788dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136166166 | ||||||
chr5:136166240 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.775+2849T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166240 | |||||||
chr5:136166305 | C | T | 1 | a0001c0001t0021g0157 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.775+2914C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166305 | |||||||
chr5:136166437 | A | G | 125 | a0001c0001t0001g0198 a0001c0001t0002g0005 a0001c0001t0002g0006 others(122): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.775+3046A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166437 | |||||||
chr5:136166510 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.775+3119A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166510 | |||||||
chr5:136166571 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.775+3180A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166571 | |||||||
chr5:136166712 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+3321A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166712 | |||||||
chr5:136166728 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.775+3337C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166728 | |||||||
chr5:136166786 | T | C | 2 | a0001c0001t0015g0022 a0001c0001t0015g0076 |
3 | HG01167.hp2 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.775+3395T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166786 | |||||||
chr5:136166820 | C | T | 2 | a0001c0001t0009g0146 a0001c0003t0009g0147 |
2 | HG00323.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.775+3429C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166820 | |||||||
chr5:136166895 | A | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.775+3504A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166895 | |||||||
chr5:136166904 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0180 others(3): Show |
6 | HG02559.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+3513C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136166904 | |||||||
chr5:136167084 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.775+3693A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167084 | |||||||
chr5:136167170 | AT | A | 125 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(122): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.775+3790delT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136167170 | ||||||
chr5:136167181 | T | C | 1 | a0001c0001t0031g0107 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.775+3790T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167181 | |||||||
chr5:136167265 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.775+3874G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167265 | |||||||
chr5:136167289 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0136 |
2 | NA18952.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.775+3898C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167289 | |||||||
chr5:136167412 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.775+4021C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167412 | |||||||
chr5:136167460 | T | A | 1 | a0001c0001t0003g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.775+4069T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167460 | |||||||
chr5:136167670 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0081 |
4 | NA18953.hp2 NA19065.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+4279C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167670 | |||||||
chr5:136167810 | T | G | 1 | a0001c0001t0003g0035 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.775+4419T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167810 | |||||||
chr5:136167891 | G | A | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.775+4500G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136167891 | |||||||
chr5:136168296 | A | G | 1 | a0001c0001t0006g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.776-4138A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136168296 | |||||||
chr5:136168393 | GTTGTT | G | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.776-4033_776-4029d others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136168393 | ||||||
chr5:136168490 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.776-3944C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136168490 | |||||||
chr5:136169001 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.776-3433T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169001 | |||||||
chr5:136169008 | G | A | 1 | a0001c0001t0014g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.776-3426G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169008 | |||||||
chr5:136169291 | C | T | 126 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(123): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.776-3143C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169291 | |||||||
chr5:136169299 | C | T | 1 | a0001c0001t0002g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.776-3135C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169299 | |||||||
chr5:136169387 | C | T | 1 | a0001c0001t0004g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.776-3047C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169387 | |||||||
chr5:136169506 | AGTTT | A | 3 | a0001c0001t0007g0003 a0001c0001t0007g0067 a0001c0001t0030g0003 |
7 | HG02615.hp2 HG02886.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.776-2923_776-2920d others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 136169506 | ||||||
chr5:136169829 | T | C | 1 | a0001c0001t0029g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.776-2605T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169829 | |||||||
chr5:136169938 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-2496A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136169938 | |||||||
chr5:136170152 | G | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2282G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170152 | |||||||
chr5:136170264 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2170A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170264 | |||||||
chr5:136170428 | G | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-2006G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170428 | |||||||
chr5:136170606 | A | G | 4 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 others(1): Show |
5 | HG01496.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.776-1828A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170606 | |||||||
chr5:136170618 | T | C | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.776-1816T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170618 | |||||||
chr5:136170708 | T | C | 1 | a0001c0001t0014g0068 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.776-1726T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170708 | |||||||
chr5:136170774 | T | C | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-1660T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170774 | |||||||
chr5:136170788 | A | G | 8 | a0001c0001t0004g0008 a0001c0001t0004g0039 a0001c0001t0004g0040 others(5): Show |
9 | HG01258.hp2 HG01346.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.776-1646A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170788 | |||||||
chr5:136170951 | C | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-1483C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170951 | |||||||
chr5:136170985 | A | G | 1 | a0001c0001t0020g0117 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.776-1449A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136170985 | |||||||
chr5:136171008 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.776-1426A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171008 | |||||||
chr5:136171017 | C | T | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-1417C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171017 | |||||||
chr5:136171106 | G | T | 1 | a0001c0001t0003g0047 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.776-1328G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171106 | |||||||
chr5:136171157 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-1277A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171157 | |||||||
chr5:136171164 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-1270A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171164 | |||||||
chr5:136171263 | T | G | 2 | a0001c0001t0013g0064 a0001c0001t0014g0068 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.776-1171T>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171263 | |||||||
chr5:136171374 | A | G | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-1060A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171374 | |||||||
chr5:136171457 | C | G | 1 | a0001c0001t0002g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.776-977C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171457 | |||||||
chr5:136171565 | C | T | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-869C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171565 | |||||||
chr5:136171590 | T | A | 1 | a0001c0001t0001g0013 | 3 | NA18964.hp1 NA18988.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.776-844T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171590 | |||||||
chr5:136171720 | T | C | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.776-714T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171720 | |||||||
chr5:136171878 | A | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-556A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171878 | |||||||
chr5:136171935 | T | C | 1 | a0001c0001t0018g0015 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.776-499T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136171935 | |||||||
chr5:136172133 | C | G | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.776-301C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172133 | |||||||
chr5:136172190 | C | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.776-244C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172190 | |||||||
chr5:136172217 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.776-217C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172217 | |||||||
chr5:136172243 | G | A | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.776-191G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172243 | |||||||
chr5:136172425 | T | C | 2 | a0001c0001t0003g0016 a0001c0001t0003g0055 |
3 | NA18961.hp2 NA18965.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.776-9T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 5/7 | chr5 | 136172425 | |||||||
chr5:136172692 | A | G | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.997+37A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172692 | |||||||
chr5:136172722 | A | G | 8 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(5): Show |
10 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.997+67A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172722 | |||||||
chr5:136172797 | G | A | 1 | a0001c0001t0013g0064 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.997+142G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136172797 | |||||||
chr5:136173225 | C | CA | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.997+571dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 136173225 | ||||||
chr5:136173286 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.997+631G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173286 | |||||||
chr5:136173418 | A | G | 3 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0139 |
3 | NA18947.hp1 NA19056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.997+763A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173418 | |||||||
chr5:136173541 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.998-835T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173541 | |||||||
chr5:136173597 | T | A | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.998-779T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173597 | |||||||
chr5:136173654 | T | C | 1 | a0001c0001t0002g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.998-722T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173654 | |||||||
chr5:136173756 | T | C | 3 | a0001c0001t0013g0075 a0001c0001t0014g0130 a0001c0001t0014g0131 |
3 | HG01496.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.998-620T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173756 | |||||||
chr5:136173912 | C | G | 2 | a0001c0001t0017g0070 a0001c0001t0017g0072 |
2 | HG02572.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.998-464C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173912 | |||||||
chr5:136173941 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0149 others(2): Show |
10 | NA18941.hp1 NA18964.hp1 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.998-435T>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136173941 | |||||||
chr5:136173943 | G | GT | 7 | a0001c0001t0003g0045 a0001c0001t0005g0028 a0001c0001t0005g0125 others(4): Show |
8 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.998-424dupT | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr5 | 136173943 | ||||||
chr5:136174032 | G | C | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-344G>C | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174032 | |||||||
chr5:136174163 | C | A | 123 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(120): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.998-213C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174163 | |||||||
chr5:136174163 | C | G | 1 | a0001c0001t0005g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.998-213C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174163 | |||||||
chr5:136174183 | C | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-193C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174183 | |||||||
chr5:136174328 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0209 |
2 | HG01069.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.998-48A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174328 | |||||||
chr5:136174344 | T | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.998-32T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174344 | |||||||
chr5:136174349 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.998-27G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174349 | |||||||
chr5:136174365 | G | A | 6 | a0001c0001t0005g0028 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-11G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 6/7 | chr5 | 136174365 | |||||||
chr5:136174741 | C | G | 59 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(56): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1254+109C>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136174741 | |||||||
chr5:136175057 | CAA | C | 59 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(56): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.1254+427_1254+428d others(4): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136175057 | ||||||
chr5:136175470 | T | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1254+838T>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175470 | |||||||
chr5:136175517 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1254+885A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175517 | |||||||
chr5:136175521 | A | G | 1 | a0001c0001t0003g0047 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1254+889A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175521 | |||||||
chr5:136175687 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1254+1055C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175687 | |||||||
chr5:136175852 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0199 |
2 | HG01106.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1254+1220C>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175852 | |||||||
chr5:136175878 | G | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1254+1246G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175878 | |||||||
chr5:136175988 | A | G | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1255-1349A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136175988 | |||||||
chr5:136176176 | G | A | 3 | a0001c0001t0001g0174 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG00621.hp1 NA18970.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1255-1161G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176176 | |||||||
chr5:136176387 | G | A | 2 | a0001c0001t0016g0077 a0001c0001t0016g0078 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1255-950G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176387 | |||||||
chr5:136176406 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0012g0038 |
3 | NA19056.hp1 NA19068.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1255-931G>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176406 | |||||||
chr5:136176457 | C | CA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0142 a0001c0001t0001g0154 others(13): Show |
17 | HG00423.hp1 HG00621.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1255-854dupA | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | C | CAAA | 2 | a0001c0001t0007g0003 a0001c0001t0030g0003 |
6 | HG02615.hp2 HG02976.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-856_1255-854d others(5): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | C | CAAAAAAA others(1): Show |
4 | a0001c0001t0005g0028 a0001c0001t0005g0128 a0001c0001t0005g0129 others(1): Show |
6 | HG01069.hp2 HG01884.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-861_1255-854d others(10): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0012g0036 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1255-868_1255-854d others(17): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0012g0037 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1255-876_1255-854d others(25): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0012g0038 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1255-878_1255-854d others(27): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | CAAAA | C | 10 | a0001c0001t0002g0119 a0001c0001t0003g0056 a0001c0001t0003g0061 others(7): Show |
11 | HG01496.hp2 HG02257.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255-857_1255-854d others(6): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | CAAAAA | C | 90 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(87): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1255-858_1255-854d others(7): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | CAAAAAA | C | 6 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0003g0045 others(3): Show |
6 | HG02602.hp1 HG02735.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1255-859_1255-854d others(8): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176457 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0013g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1255-866_1255-854d others(15): Show |
SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 136176457 | ||||||
chr5:136176833 | G | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0184 a0001c0001t0001g0185 |
3 | HG00621.hp1 NA18970.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1255-504G>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176833 | |||||||
chr5:136176983 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0002g0105 |
2 | HG01928.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1255-354A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136176983 | |||||||
chr5:136177077 | A | T | 1 | a0001c0001t0029g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1255-260A>T | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177077 | |||||||
chr5:136177227 | C | A | 124 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0010 others(121): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1255-110C>A | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177227 | |||||||
chr5:136177248 | A | G | 1 | a0001c0001t0002g0104 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1255-89A>G | SMAD5 | ENSG00000113658.18 | transcript | ENST00000545279.6 | protein_coding | 7/7 | chr5 | 136177248 |