Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 341346 |
| ensemblid | ENSG00000165935.10 |
| hgncid | 34448 |
| symbol | SMCO2 |
| name | single-pass membrane protein with coiled-coil domains 2 |
| refseq_nuc | NM_001395208.2 |
| refseq_prot | NP_001382137.1 |
| ensembl_nuc | ENST00000535986.2 |
| ensembl_prot | ENSP00000441688.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 27446736 |
| end | 27502185 |
| strand | + |
| ver | v1.2 |
| region | chr12:27446736-27502185 |
| region5000 | chr12:27441736-27507185 |
| regionname0 | SMCO2_chr12_27446736_27502185 |
| regionname5000 | SMCO2_chr12_27441736_27507185 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 343 | 183 | 34 | 41 | 69 | 12 | 25 | 52 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(338): Show |
chr12 | 27441736 | 27507185 |
| a0002 | 0/0 | 343 | 152 | 41 | 9 | 84 | 1 | 17 | 70 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(338): Show |
chr12 | 27441736 | 27507185 |
| a0003 | 0/0 | 219 | 16 | 13 | 2 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(214): Show |
chr12 | 27441736 | 27507185 |
| a0004 | 0/0 | 219 | 5 | 0 | 0 | 3 | 0 | 2 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(214): Show |
chr12 | 27441736 | 27507185 |
| a0005 | 0/0 | 343 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(338): Show |
chr12 | 27441736 | 27507185 |
| a0006 | 0/0 | 343 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(338): Show |
chr12 | 27441736 | 27507185 |
| a0007 | 0/0 | 343 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | MALTP others(338): Show |
chr12 | 27441736 | 27507185 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1029 | 174 | 34 | 37 | 69 | 8 | 25 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0001c0005 | 1/0 | 1029 | 9 | 0 | 4 | 0 | 4 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0002c0002 | 0/0 | 1029 | 94 | 26 | 7 | 48 | 0 | 13 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0002c0003 | 0/0 | 1029 | 53 | 10 | 2 | 36 | 1 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0002c0007 | 0/0 | 1029 | 4 | 4 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0002c0012 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0003c0004 | 0/0 | 657 | 13 | 10 | 2 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(652): Show |
chr12 | 27441736 | 27507185 | ||
| a0003c0009 | 0/0 | 657 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(652): Show |
chr12 | 27441736 | 27507185 | ||
| a0003c0013 | 0/0 | 657 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(652): Show |
chr12 | 27441736 | 27507185 | ||
| a0004c0006 | 0/0 | 657 | 5 | 0 | 0 | 3 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(652): Show |
chr12 | 27441736 | 27507185 | ||
| a0005c0008 | 0/0 | 1029 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0006c0011 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 | ||
| a0007c0010 | 0/0 | 1029 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | ATGGC others(1024): Show |
chr12 | 27441736 | 27507185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1196 | 122 | 29 | 31 | 37 | 8 | 17 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0001c0001t0002 | 0/1 | 1196 | 49 | 5 | 4 | 32 | 0 | 7 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0001c0001t0004 | 0/0 | 1196 | 3 | 0 | 2 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0001c0005t0002 | 1/0 | 1196 | 9 | 0 | 4 | 0 | 4 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0002t0001 | 0/0 | 1196 | 12 | 10 | 1 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0002t0002 | 0/0 | 1196 | 64 | 3 | 4 | 47 | 0 | 10 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0002t0003 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0002t0004 | 0/0 | 1196 | 17 | 12 | 2 | 0 | 0 | 3 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0003t0001 | 0/0 | 1196 | 8 | 7 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0003t0003 | 0/0 | 1196 | 41 | 1 | 1 | 35 | 0 | 4 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0003t0004 | 0/0 | 1196 | 4 | 2 | 0 | 1 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0007t0001 | 0/0 | 1196 | 4 | 4 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0002c0012t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0003c0004t0005 | 0/0 | 757 | 10 | 10 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(752): Show |
chr12 | 27441736 | 27507185 |
| a0003c0004t0006 | 0/0 | 757 | 3 | 0 | 2 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(752): Show |
chr12 | 27441736 | 27507185 |
| a0003c0009t0005 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(752): Show |
chr12 | 27441736 | 27507185 |
| a0003c0013t0006 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(752): Show |
chr12 | 27441736 | 27507185 |
| a0004c0006t0006 | 0/0 | 757 | 5 | 0 | 0 | 3 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(752): Show |
chr12 | 27441736 | 27507185 |
| a0005c0008t0001 | 0/0 | 1196 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0006c0011t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| a0007c0010t0001 | 0/0 | 1196 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | AGTGG others(1191): Show |
chr12 | 27441736 | 27507185 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0277 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0001c0005t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0002t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0003t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0007t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0002c0012t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0006g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0004t0006g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0009t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0003c0013t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0006t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0006t0006g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0006t0006g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0006t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0004c0006t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0005c0008t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0005c0008t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0006c0011t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| a0007c0010t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00099 | hp2 | a0003 | c0004 | t0006 | g0053 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00140 | hp2 | a0001 | c0005 | t0002 | g0066 | EUR | GBR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00280 | hp1 | a0001 | c0005 | t0002 | g0008 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00323 | hp1 | a0001 | c0005 | t0002 | g0064 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00609 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00642 | hp2 | a0002 | c0003 | t0001 | g0211 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0068 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01069 | hp1 | a0001 | c0005 | t0002 | g0063 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01069 | hp2 | a0003 | c0004 | t0006 | g0015 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01070 | hp1 | a0001 | c0005 | t0002 | g0065 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01071 | hp2 | a0003 | c0004 | t0006 | g0015 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0034 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01169 | hp2 | a0002 | c0002 | t0004 | g0034 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01361 | hp2 | a0001 | c0005 | t0002 | g0008 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0243 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0061 | AMR | CLM | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01517 | hp2 | a0001 | c0005 | t0002 | g0008 | EUR | IBS | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01884 | hp1 | a0002 | c0007 | t0001 | g0215 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01884 | hp2 | a0002 | c0003 | t0004 | g0258 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0271 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02004 | hp1 | a0002 | c0003 | t0003 | g0141 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02015 | hp2 | a0004 | c0006 | t0006 | g0292 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02027 | hp2 | a0002 | c0003 | t0003 | g0140 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02055 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02080 | hp1 | a0002 | c0003 | t0003 | g0130 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0265 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0135 | EAS | CDX | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02257 | hp1 | a0002 | c0007 | t0001 | g0274 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02257 | hp2 | a0002 | c0002 | t0004 | g0273 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02258 | hp2 | a0003 | c0004 | t0005 | g0032 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02280 | hp1 | a0002 | c0003 | t0003 | g0133 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0266 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02572 | hp2 | a0006 | c0011 | t0001 | g0036 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0025 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0186 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02622 | hp1 | a0007 | c0010 | t0001 | g0232 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02622 | hp2 | a0002 | c0003 | t0001 | g0192 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0222 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02717 | hp2 | a0003 | c0004 | t0005 | g0252 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02723 | hp1 | a0005 | c0008 | t0001 | g0278 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02735 | hp2 | a0004 | c0006 | t0006 | g0291 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02818 | hp1 | a0003 | c0004 | t0005 | g0257 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02818 | hp2 | a0002 | c0002 | t0004 | g0268 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02895 | hp1 | a0003 | c0004 | t0005 | g0256 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02896 | hp2 | a0002 | c0002 | t0004 | g0269 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02897 | hp1 | a0002 | c0002 | t0004 | g0270 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02922 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02965 | hp1 | a0003 | c0004 | t0005 | g0023 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0263 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02976 | hp2 | a0003 | c0009 | t0005 | g0040 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03017 | hp2 | a0004 | c0006 | t0006 | g0293 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03041 | hp2 | a0005 | c0008 | t0001 | g0279 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03098 | hp1 | a0002 | c0002 | t0004 | g0245 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03139 | hp1 | a0002 | c0007 | t0001 | g0275 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03195 | hp1 | a0002 | c0007 | t0001 | g0276 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03195 | hp2 | a0002 | c0012 | t0001 | g0039 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03209 | hp2 | a0003 | c0009 | t0005 | g0044 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0041 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03239 | hp2 | a0002 | c0003 | t0003 | g0146 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0267 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03516 | hp1 | a0003 | c0004 | t0005 | g0254 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03516 | hp2 | a0002 | c0002 | t0004 | g0272 | AFR | ESN | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0027 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03688 | hp2 | a0002 | c0003 | t0003 | g0022 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0025 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03831 | hp1 | a0002 | c0003 | t0003 | g0022 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0104 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03834 | hp1 | a0002 | c0003 | t0003 | g0152 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0106 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04115 | hp1 | a0002 | c0002 | t0004 | g0184 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | BEB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0109 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | STU | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0092 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18939 | hp1 | a0002 | c0003 | t0003 | g0144 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18940 | hp2 | a0002 | c0003 | t0003 | g0035 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18942 | hp1 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18944 | hp1 | a0002 | c0003 | t0003 | g0134 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18945 | hp2 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18952 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0137 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18961 | hp2 | a0002 | c0003 | t0003 | g0129 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18962 | hp1 | a0002 | c0003 | t0004 | g0165 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18962 | hp2 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18968 | hp2 | a0002 | c0003 | t0003 | g0145 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0035 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18980 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18983 | hp2 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0148 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18986 | hp2 | a0004 | c0006 | t0006 | g0290 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18988 | hp1 | a0002 | c0003 | t0003 | g0132 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18989 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18990 | hp2 | a0002 | c0003 | t0003 | g0142 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18998 | hp1 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19002 | hp2 | a0002 | c0003 | t0003 | g0150 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0143 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19005 | hp2 | a0002 | c0003 | t0003 | g0131 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19007 | hp1 | a0002 | c0003 | t0003 | g0011 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19011 | hp1 | a0004 | c0006 | t0006 | g0214 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0100 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0149 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19063 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19078 | hp1 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0147 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19087 | hp1 | a0002 | c0003 | t0003 | g0151 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0001 | EAS | JPT | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19240 | hp1 | a0003 | c0004 | t0005 | g0255 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20129 | hp1 | a0003 | c0013 | t0006 | g0050 | AFR | ASW | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20129 | hp2 | a0002 | c0002 | t0004 | g0264 | AFR | ASW | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20752 | hp1 | a0002 | c0003 | t0004 | g0233 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | GIH | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02109 | hp2 | a0002 | c0003 | t0001 | g0189 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0287 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG03471 | hp2 | a0003 | c0004 | t0005 | g0253 | AFR | MSL | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA20300 | hp2 | a0003 | c0004 | t0005 | g0032 | AFR | USA | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA21309 | hp1 | a0002 | c0003 | t0004 | g0161 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0251 | AFR | LWK | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0277 | REF | REF | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0002 | g0062 | REF | REF | SMCO2_chr12_27441736_27507185 | SMCO2 | chr12 | 27441736 | 27507185 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27472846 | G | A | 1 | a0007 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.205G>A | p.Glu69Lys | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/9 | 305/1196 | 205/1032 | 69/343 | chr12 | 27472846 | |||
| chr12:27475674 | C | T | 2 | a0004 a0006 |
6 | HG02015.hp2 HG02572.hp2 HG02735.hp2 others(3): Show |
missense_variant | MODERATE | c.455C>T | p.Thr152Met | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 555/1196 | 455/1032 | 152/343 | chr12 | 27475674 | |||
| chr12:27475679 | A | G | 1 | a0005 | 2 | HG02723.hp1 HG03041.hp2 |
missense_variant | MODERATE | c.460A>G | p.Lys154Glu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 560/1196 | 460/1032 | 154/343 | chr12 | 27475679 | |||
| chr12:27488540 | G | A | 4 | a0002 a0003 a0004 others(1): Show |
175 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
missense_variant | MODERATE | c.593G>A | p.Ser198Asn | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/9 | 693/1196 | 593/1032 | 198/343 | chr12 | 27488540 | |||
| chr12:27495209 | GTTTTCTC others(7014): Show |
G | 2 | a0003 a0004 |
21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
exon_loss_variant | HIGH | c.658-470_*109del | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | chr12 | 27495209 | |||||||
| chr12:27495777 | C | T | 2 | a0001 a0002 |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
missense_variant | MODERATE | c.755C>T | p.Thr252Met | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 855/1196 | 755/1032 | 252/343 | chr12 | 27495777 | |||
| chr12:27502065 | C | T | 1 | a0001 | 2 | HG03209.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.976C>T | p.Arg326Trp | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 9/9 | 1076/1196 | 976/1032 | 326/343 | chr12 | 27502065 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27474822 | C | T | 1 | a0003c0013 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.271C>T | p.Leu91Leu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/9 | 371/1196 | 271/1032 | 91/343 | chr12 | 27474822 | |||
| chr12:27474872 | G | A | 7 | a0001c0001 a0002c0003 a0002c0007 others(4): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
synonymous_variant | LOW | c.321G>A | p.Ala107Ala | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/9 | 421/1196 | 321/1032 | 107/343 | chr12 | 27474872 | |||
| chr12:27475588 | G | C | 2 | a0002c0012 a0003c0009 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.369G>C | p.Leu123Leu | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 469/1196 | 369/1032 | 123/343 | chr12 | 27475588 | |||
| chr12:27475594 | C | T | 1 | a0002c0007 | 4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.375C>T | p.Gly125Gly | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/9 | 475/1196 | 375/1032 | 125/343 | chr12 | 27475594 | |||
| chr12:27488532 | A | G | 2 | a0002c0012 a0003c0009 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.585A>G | p.Gln195Gln | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/9 | 685/1196 | 585/1032 | 195/343 | chr12 | 27488532 | |||
| chr12:27495727 | T | C | 1 | a0002c0003 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.705T>C | p.Tyr235Tyr | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 805/1196 | 705/1032 | 235/343 | chr12 | 27495727 | |||
| chr12:27495844 | C | T | 3 | a0001c0001 a0002c0003 a0002c0007 |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
synonymous_variant | LOW | c.822C>T | p.Arg274Arg | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 922/1196 | 822/1032 | 274/343 | chr12 | 27495844 | |||
| chr12:27495853 | A | G | 5 | a0001c0001 a0002c0002 a0002c0003 others(2): Show |
150 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(147): Show |
splice_region_variant&synonymous_variant | LOW | c.831A>G | p.Ala277Ala | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/9 | 931/1196 | 831/1032 | 277/343 | chr12 | 27495853 | |||
| chr12:27501965 | C | T | 1 | a0001c0001 | 22 | HG00099.hp1 HG00323.hp2 HG00673.hp2 others(19): Show |
synonymous_variant | LOW | c.876C>T | p.Thr292Thr | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 9/9 | 976/1196 | 876/1032 | 292/343 | chr12 | 27501965 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27446766 | G | T | 16 | a0001c0001t0001 a0001c0001t0004 a0002c0002t0001 others(13): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/9 | 23866 | chr12 | 27446766 | ||||||
| chr12:27446770 | T | C | 16 | a0001c0001t0001 a0001c0001t0004 a0002c0002t0001 others(13): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/9 | chr12 | 27446770 | |||||||
| chr12:27470625 | C | T | 8 | a0001c0001t0004 a0002c0002t0003 a0002c0002t0004 others(5): Show |
75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/9 | chr12 | 27470625 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:27446836 | G | T | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+11G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27446836 | |||||||
| chr12:27447001 | G | A | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+176G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447001 | |||||||
| chr12:27447035 | G | T | 1 | a0001c0001t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+210G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447035 | |||||||
| chr12:27447043 | G | T | 9 | a0001c0001t0001g0281 a0001c0001t0002g0037 a0001c0001t0002g0282 others(6): Show |
10 | HG01255.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+218G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447043 | |||||||
| chr12:27447084 | A | T | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-11+259A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447084 | |||||||
| chr12:27447227 | G | C | 21 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(18): Show |
22 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11+402G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447227 | |||||||
| chr12:27447349 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-11+524C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447349 | |||||||
| chr12:27447384 | C | T | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+559C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447384 | |||||||
| chr12:27447398 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(244): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-11+573C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447398 | |||||||
| chr12:27447437 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-11+612G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447437 | |||||||
| chr12:27447450 | C | T | 2 | a0001c0001t0001g0036 a0006c0011t0001g0036 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-11+625C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447450 | |||||||
| chr12:27447547 | C | T | 1 | a0002c0003t0003g0035 | 2 | NA18940.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-11+722C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447547 | |||||||
| chr12:27447554 | C | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(165): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-11+729C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447554 | |||||||
| chr12:27447614 | T | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(151): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-11+789T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447614 | |||||||
| chr12:27447728 | CA | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(188): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.-11+920delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27447728 | ||||||
| chr12:27447760 | C | G | 6 | a0001c0001t0002g0019 a0001c0001t0002g0089 a0001c0001t0002g0090 others(3): Show |
7 | HG00544.hp2 NA18747.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+935C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447760 | |||||||
| chr12:27447776 | T | TG | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+952dupG | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27447776 | ||||||
| chr12:27447896 | G | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(145): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-11+1071G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447896 | |||||||
| chr12:27447906 | C | T | 152 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(149): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-11+1081C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27447906 | |||||||
| chr12:27448132 | G | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0003c0013t0006g0050 |
3 | HG02055.hp2 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-11+1307G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448132 | |||||||
| chr12:27448350 | G | A | 7 | a0001c0001t0002g0016 a0001c0001t0002g0055 a0001c0001t0002g0056 others(4): Show |
8 | HG01975.hp2 HG02155.hp2 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+1525G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448350 | |||||||
| chr12:27448460 | C | T | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1635C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448460 | |||||||
| chr12:27448488 | A | G | 12 | a0001c0001t0001g0281 a0001c0001t0002g0037 a0001c0001t0002g0282 others(9): Show |
13 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+1663A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448488 | |||||||
| chr12:27448503 | T | C | 11 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+1678T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448503 | |||||||
| chr12:27448538 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-11+1713C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448538 | |||||||
| chr12:27448903 | G | T | 1 | a0001c0001t0001g0033 | 2 | HG01192.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-11+2078G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448903 | |||||||
| chr12:27448992 | C | T | 11 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(8): Show |
12 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+2167C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27448992 | |||||||
| chr12:27449024 | A | C | 9 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+2199A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449024 | |||||||
| chr12:27449190 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(204): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11+2365A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449190 | |||||||
| chr12:27449207 | G | A | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+2382G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449207 | |||||||
| chr12:27449252 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(160): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-11+2427G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449252 | |||||||
| chr12:27449315 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-11+2490T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449315 | |||||||
| chr12:27449341 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-11+2516G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449341 | |||||||
| chr12:27449880 | G | A | 9 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(6): Show |
9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+3055G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449880 | |||||||
| chr12:27449930 | C | T | 1 | a0002c0002t0002g0088 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-11+3105C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449930 | |||||||
| chr12:27449954 | G | T | 37 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(34): Show |
45 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.-11+3129G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449954 | |||||||
| chr12:27449991 | G | A | 1 | a0002c0003t0003g0129 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-11+3166G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27449991 | |||||||
| chr12:27450307 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-11+3482C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450307 | |||||||
| chr12:27450308 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(204): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-11+3483A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450308 | |||||||
| chr12:27450421 | A | C | 1 | a0001c0001t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-11+3596A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450421 | |||||||
| chr12:27450521 | G | A | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+3696G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450521 | |||||||
| chr12:27450566 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-11+3741C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450566 | |||||||
| chr12:27450608 | G | C | 15 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-11+3783G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450608 | |||||||
| chr12:27450684 | G | A | 7 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-11+3859G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450684 | |||||||
| chr12:27450774 | A | G | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+3949A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27450774 | |||||||
| chr12:27451027 | C | T | 11 | a0001c0001t0002g0037 a0001c0001t0002g0282 a0001c0001t0002g0283 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+4202C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451027 | |||||||
| chr12:27451043 | C | A | 1 | a0002c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+4218C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451043 | |||||||
| chr12:27451274 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-11+4449A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451274 | |||||||
| chr12:27451330 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(175): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-11+4505G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451330 | |||||||
| chr12:27451332 | A | G | 1 | a0002c0003t0003g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-11+4507A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451332 | |||||||
| chr12:27451502 | A | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(137): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-11+4677A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451502 | |||||||
| chr12:27451693 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+4868C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451693 | |||||||
| chr12:27451703 | C | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG01255.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+4878C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451703 | |||||||
| chr12:27451778 | A | C | 12 | a0001c0001t0001g0281 a0001c0001t0002g0037 a0001c0001t0002g0282 others(9): Show |
13 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+4953A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451778 | |||||||
| chr12:27451818 | G | A | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+4993G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451818 | |||||||
| chr12:27451842 | T | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.-11+5017T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451842 | |||||||
| chr12:27451889 | C | T | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+5064C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27451889 | |||||||
| chr12:27452017 | G | A | 20 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0003t0001g0251 others(17): Show |
24 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-11+5192G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452017 | |||||||
| chr12:27452129 | G | A | 2 | a0002c0007t0001g0274 a0002c0007t0001g0275 |
2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-11+5304G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452129 | |||||||
| chr12:27452331 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-11+5506C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452331 | |||||||
| chr12:27452505 | G | A | 11 | a0001c0001t0002g0037 a0001c0001t0002g0282 a0001c0001t0002g0283 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+5680G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452505 | |||||||
| chr12:27452565 | C | G | 9 | a0001c0001t0001g0033 a0003c0004t0005g0023 a0003c0004t0005g0032 others(6): Show |
12 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+5740C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452565 | |||||||
| chr12:27452572 | C | G | 4 | a0002c0002t0004g0268 a0002c0002t0004g0269 a0002c0002t0004g0270 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+5747C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452572 | |||||||
| chr12:27452693 | C | T | 12 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+5868C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452693 | |||||||
| chr12:27452853 | A | G | 9 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(6): Show |
12 | HG02109.hp1 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+6028A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452853 | |||||||
| chr12:27452921 | G | A | 12 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+6096G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452921 | |||||||
| chr12:27452925 | C | T | 12 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(9): Show |
13 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+6100C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27452925 | |||||||
| chr12:27453028 | C | T | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11+6203C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453028 | |||||||
| chr12:27453055 | A | G | 29 | a0002c0002t0002g0135 a0002c0002t0002g0138 a0002c0003t0003g0001 others(26): Show |
42 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11+6230A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453055 | |||||||
| chr12:27453106 | C | T | 29 | a0002c0002t0002g0135 a0002c0002t0002g0138 a0002c0003t0003g0001 others(26): Show |
42 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11+6281C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453106 | |||||||
| chr12:27453136 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(181): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-11+6311T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453136 | |||||||
| chr12:27453357 | G | A | 9 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(6): Show |
9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+6532G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453357 | |||||||
| chr12:27453537 | A | G | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+6712A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453537 | |||||||
| chr12:27453626 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-11+6801C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453626 | |||||||
| chr12:27453749 | G | A | 9 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(6): Show |
9 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-11+6924G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453749 | |||||||
| chr12:27453751 | G | T | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+6926G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453751 | |||||||
| chr12:27453853 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
6 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+7028A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453853 | |||||||
| chr12:27453868 | T | G | 1 | a0002c0002t0002g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-11+7043T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453868 | |||||||
| chr12:27453899 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+7074C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453899 | |||||||
| chr12:27453931 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+7106C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27453931 | |||||||
| chr12:27454024 | A | G | 197 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(194): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-11+7199A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454024 | |||||||
| chr12:27454173 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01192.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-11+7348C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454173 | |||||||
| chr12:27454258 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(170): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-11+7433A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454258 | |||||||
| chr12:27454332 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11+7507G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454332 | |||||||
| chr12:27454389 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-11+7564C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454389 | |||||||
| chr12:27454396 | G | A | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+7571G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454396 | |||||||
| chr12:27454455 | T | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(178): Show |
221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.-11+7630T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454455 | |||||||
| chr12:27454517 | T | C | 1 | a0002c0003t0004g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-11+7692T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454517 | |||||||
| chr12:27454548 | C | T | 2 | a0002c0003t0003g0150 a0002c0003t0003g0151 |
2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-11+7723C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454548 | |||||||
| chr12:27454710 | T | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(170): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-11+7885T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454710 | |||||||
| chr12:27454743 | G | A | 11 | a0001c0001t0002g0037 a0001c0001t0002g0282 a0001c0001t0002g0283 others(8): Show |
12 | HG01255.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-11+7918G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454743 | |||||||
| chr12:27454910 | C | CT | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-11+8091dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27454910 | ||||||
| chr12:27454998 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-11+8173C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27454998 | |||||||
| chr12:27455190 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(174): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-11+8365A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455190 | |||||||
| chr12:27455228 | C | G | 1 | a0002c0003t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-11+8403C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455228 | |||||||
| chr12:27455339 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-11+8514A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455339 | |||||||
| chr12:27455385 | A | G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG01255.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-11+8560A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455385 | |||||||
| chr12:27455487 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+8662A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455487 | |||||||
| chr12:27455624 | A | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(179): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-11+8799A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455624 | |||||||
| chr12:27455670 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-11+8845T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455670 | |||||||
| chr12:27455691 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(179): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-11+8866G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455691 | |||||||
| chr12:27455730 | T | C | 1 | a0001c0001t0002g0017 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-11+8905T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455730 | |||||||
| chr12:27455783 | G | A | 28 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(25): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+8958G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455783 | |||||||
| chr12:27455826 | G | A | 28 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(25): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+9001G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455826 | |||||||
| chr12:27455838 | G | C | 1 | a0002c0002t0001g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-11+9013G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455838 | |||||||
| chr12:27455976 | G | A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | NA18962.hp1 NA18978.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+9151G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455976 | |||||||
| chr12:27455978 | G | A | 2 | a0003c0004t0005g0252 a0003c0004t0005g0253 |
2 | HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-11+9153G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27455978 | |||||||
| chr12:27456000 | G | A | 1 | a0002c0002t0002g0098 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-11+9175G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456000 | |||||||
| chr12:27456063 | G | A | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-11+9238G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456063 | |||||||
| chr12:27456086 | A | T | 3 | a0002c0003t0004g0258 a0005c0008t0001g0278 a0005c0008t0001g0279 |
3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+9261A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456086 | |||||||
| chr12:27456107 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-11+9282C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456107 | |||||||
| chr12:27456140 | G | A | 123 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(120): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-11+9315G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456140 | |||||||
| chr12:27456163 | C | T | 24 | a0001c0001t0001g0033 a0002c0002t0001g0041 a0002c0002t0001g0042 others(21): Show |
28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+9338C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456163 | |||||||
| chr12:27456185 | A | G | 1 | a0002c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11+9360A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456185 | |||||||
| chr12:27456202 | T | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(146): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11+9377T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456202 | |||||||
| chr12:27456247 | T | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(146): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11+9422T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456247 | |||||||
| chr12:27456323 | T | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-11+9498T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456323 | |||||||
| chr12:27456343 | G | A | 10 | a0001c0001t0001g0033 a0002c0003t0001g0251 a0003c0004t0005g0023 others(7): Show |
13 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+9518G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456343 | |||||||
| chr12:27456365 | G | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0089 a0001c0001t0002g0090 others(1): Show |
5 | HG00544.hp2 NA18975.hp1 NA19063.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+9540G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456365 | |||||||
| chr12:27456384 | T | G | 4 | a0002c0003t0004g0258 a0003c0013t0006g0050 a0005c0008t0001g0278 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9559T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456384 | |||||||
| chr12:27456461 | G | T | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+9636G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456461 | |||||||
| chr12:27456476 | G | A | 10 | a0001c0001t0001g0033 a0002c0003t0001g0251 a0003c0004t0005g0023 others(7): Show |
13 | HG01192.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+9651G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456476 | |||||||
| chr12:27456499 | G | T | 1 | a0007c0010t0001g0232 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+9674G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456499 | |||||||
| chr12:27456513 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-11+9688G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456513 | |||||||
| chr12:27456525 | C | A | 1 | a0003c0004t0006g0053 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-11+9700C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456525 | |||||||
| chr12:27456560 | G | A | 1 | a0002c0002t0002g0068 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-11+9735G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456560 | |||||||
| chr12:27456578 | C | G | 4 | a0002c0003t0004g0258 a0003c0013t0006g0050 a0005c0008t0001g0278 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9753C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456578 | |||||||
| chr12:27456592 | G | T | 9 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+9767G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456592 | |||||||
| chr12:27456737 | T | C | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+9912T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456737 | |||||||
| chr12:27456943 | C | T | 3 | a0002c0003t0004g0258 a0005c0008t0001g0278 a0005c0008t0001g0279 |
3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+10118C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27456943 | |||||||
| chr12:27457140 | C | T | 2 | a0001c0001t0001g0231 a0001c0001t0001g0259 |
2 | HG01192.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-11+10315C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457140 | |||||||
| chr12:27457141 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-11+10316G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457141 | |||||||
| chr12:27457164 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+10339G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457164 | |||||||
| chr12:27457265 | G | A | 3 | a0002c0003t0004g0258 a0005c0008t0001g0278 a0005c0008t0001g0279 |
3 | HG01884.hp2 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-11+10440G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457265 | |||||||
| chr12:27457413 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+10588C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457413 | |||||||
| chr12:27457514 | C | G | 33 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(30): Show |
46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-11+10689C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457514 | |||||||
| chr12:27457571 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-11+10746C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457571 | |||||||
| chr12:27457637 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(187): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-11+10812A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457637 | |||||||
| chr12:27457640 | G | A | 35 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(32): Show |
48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-11+10815G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457640 | |||||||
| chr12:27457855 | T | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02451.hp2 HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+11030T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457855 | |||||||
| chr12:27457868 | G | A | 24 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(21): Show |
28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+11043G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457868 | |||||||
| chr12:27457869 | G | T | 24 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(21): Show |
28 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-11+11044G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457869 | |||||||
| chr12:27457988 | G | T | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-11+11163G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27457988 | |||||||
| chr12:27458163 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(119): Show |
145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-11+11338C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458163 | |||||||
| chr12:27458414 | C | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG02451.hp2 HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+11589C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458414 | |||||||
| chr12:27458445 | C | G | 28 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(25): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-11+11620C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458445 | |||||||
| chr12:27458480 | A | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(121): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.-11+11655A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458480 | |||||||
| chr12:27458649 | G | A | 2 | a0002c0002t0004g0272 a0002c0002t0004g0273 |
2 | HG02257.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-11+11824G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458649 | |||||||
| chr12:27458690 | A | C | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-11+11865A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458690 | |||||||
| chr12:27458773 | G | A | 1 | a0002c0003t0003g0130 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-10-11849G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458773 | |||||||
| chr12:27458834 | C | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0172 |
7 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-11788C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458834 | |||||||
| chr12:27458874 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-10-11748G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458874 | |||||||
| chr12:27458888 | G | GA | 15 | a0001c0001t0001g0033 a0001c0001t0001g0162 a0001c0001t0001g0236 others(12): Show |
19 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-10-11717dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27458888 | ||||||
| chr12:27458972 | T | G | 32 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(29): Show |
36 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-11650T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27458972 | |||||||
| chr12:27459080 | G | A | 1 | a0002c0003t0003g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-10-11542G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459080 | |||||||
| chr12:27459112 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-10-11510G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459112 | |||||||
| chr12:27459131 | G | C | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-11491G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459131 | |||||||
| chr12:27459135 | C | T | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11487C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459135 | |||||||
| chr12:27459174 | A | G | 12 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(9): Show |
12 | HG00741.hp2 HG02809.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10-11448A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459174 | |||||||
| chr12:27459186 | C | CA | 8 | a0001c0001t0002g0070 a0001c0001t0002g0103 a0002c0002t0002g0071 others(5): Show |
8 | HG03239.hp1 HG03831.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-11414dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | ||||||
| chr12:27459186 | CA | C | 60 | a0001c0001t0001g0160 a0001c0001t0001g0175 a0001c0001t0001g0176 others(57): Show |
74 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.-10-11414delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | ||||||
| chr12:27459186 | CAA | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(100): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.-10-11415_-10-1141 others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | ||||||
| chr12:27459186 | CAAA | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0156 others(14): Show |
21 | HG01168.hp2 HG02015.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.-10-11416_-10-1141 others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | ||||||
| chr12:27459186 | CAAAAAA | C | 23 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(20): Show |
27 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-10-11419_-10-1141 others(10): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27459186 | ||||||
| chr12:27459193 | A | G | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-11429A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459193 | |||||||
| chr12:27459268 | T | G | 1 | a0004c0006t0006g0291 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10-11354T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459268 | |||||||
| chr12:27459272 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-11350T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459272 | |||||||
| chr12:27459311 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0055 a0001c0001t0002g0060 |
4 | HG01975.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-11311T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459311 | |||||||
| chr12:27459351 | C | T | 4 | a0002c0003t0004g0258 a0003c0013t0006g0050 a0005c0008t0001g0278 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-11271C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459351 | |||||||
| chr12:27459384 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-10-11238T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459384 | |||||||
| chr12:27459550 | T | A | 28 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(25): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-11072T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459550 | |||||||
| chr12:27459584 | A | C | 38 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(35): Show |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-11038A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459584 | |||||||
| chr12:27459610 | G | A | 28 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0041 others(25): Show |
32 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-10-11012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27459610 | |||||||
| chr12:27460118 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-10-10504C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460118 | |||||||
| chr12:27460167 | A | G | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-10455A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460167 | |||||||
| chr12:27460168 | G | C | 19 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0003t0001g0251 others(16): Show |
23 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10-10454G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460168 | |||||||
| chr12:27460290 | C | T | 19 | a0001c0001t0001g0033 a0002c0002t0001g0038 a0002c0003t0001g0251 others(16): Show |
23 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.-10-10332C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460290 | |||||||
| chr12:27460400 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-10222A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460400 | |||||||
| chr12:27460413 | G | A | 8 | a0001c0001t0002g0037 a0001c0001t0002g0282 a0001c0001t0002g0283 others(5): Show |
9 | HG01255.hp2 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-10209G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460413 | |||||||
| chr12:27460429 | A | T | 3 | a0002c0007t0001g0274 a0002c0007t0001g0275 a0002c0007t0001g0276 |
3 | HG02257.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-10193A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460429 | |||||||
| chr12:27460556 | G | GTGA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
8 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-10064_-10-1006 others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27460556 | ||||||
| chr12:27460879 | G | A | 1 | a0002c0002t0002g0072 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-9743G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460879 | |||||||
| chr12:27460921 | C | T | 1 | a0002c0002t0002g0126 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-10-9701C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460921 | |||||||
| chr12:27460937 | G | A | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-10-9685G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27460937 | |||||||
| chr12:27461138 | A | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(136): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-10-9484A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461138 | |||||||
| chr12:27461186 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-10-9436C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461186 | |||||||
| chr12:27461323 | G | A | 38 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0002c0002t0002g0135 others(35): Show |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-9299G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461323 | |||||||
| chr12:27461342 | T | G | 8 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 others(5): Show |
8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-9280T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461342 | |||||||
| chr12:27461407 | G | A | 34 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0002c0002t0002g0135 others(31): Show |
47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-9215G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461407 | |||||||
| chr12:27461415 | C | A | 1 | a0001c0001t0002g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-10-9207C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461415 | |||||||
| chr12:27461433 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-10-9189C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461433 | |||||||
| chr12:27461534 | G | A | 1 | a0002c0002t0002g0105 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-10-9088G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461534 | |||||||
| chr12:27461607 | C | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-9015C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461607 | |||||||
| chr12:27461616 | T | C | 12 | a0001c0001t0001g0033 a0002c0003t0001g0251 a0003c0004t0005g0023 others(9): Show |
16 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10-9006T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461616 | |||||||
| chr12:27461698 | C | T | 57 | a0001c0001t0001g0033 a0001c0001t0004g0234 a0001c0001t0004g0235 others(54): Show |
74 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-10-8924C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461698 | |||||||
| chr12:27461808 | C | A | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-8814C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461808 | |||||||
| chr12:27461827 | A | G | 34 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0002c0002t0002g0135 others(31): Show |
47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-8795A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27461827 | |||||||
| chr12:27462020 | G | T | 9 | a0002c0002t0004g0034 a0002c0002t0004g0266 a0002c0002t0004g0267 others(6): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-8602G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462020 | |||||||
| chr12:27462209 | G | A | 1 | a0002c0003t0004g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-8413G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462209 | |||||||
| chr12:27462248 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-10-8374T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462248 | |||||||
| chr12:27462339 | CCTTT | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0155 a0001c0001t0001g0219 others(4): Show |
9 | HG02040.hp2 HG02165.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-8278_-10-8275d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27462339 | ||||||
| chr12:27462402 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-10-8220G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462402 | |||||||
| chr12:27462441 | A | G | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-8181A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462441 | |||||||
| chr12:27462473 | G | T | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-8149G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462473 | |||||||
| chr12:27462510 | G | A | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-8112G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462510 | |||||||
| chr12:27462532 | A | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG00642.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-10-8090A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462532 | |||||||
| chr12:27462600 | T | C | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-8022T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462600 | |||||||
| chr12:27462627 | G | A | 1 | a0002c0002t0004g0272 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-10-7995G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462627 | |||||||
| chr12:27462675 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10-7947C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462675 | |||||||
| chr12:27462736 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-10-7886A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462736 | |||||||
| chr12:27462738 | T | C | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-7884T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462738 | |||||||
| chr12:27462876 | C | G | 38 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(35): Show |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-10-7746C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462876 | |||||||
| chr12:27462881 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-10-7741C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27462881 | |||||||
| chr12:27463084 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-10-7538C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463084 | |||||||
| chr12:27463151 | C | T | 4 | a0002c0003t0004g0258 a0003c0013t0006g0050 a0005c0008t0001g0278 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-7471C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463151 | |||||||
| chr12:27463248 | C | A | 47 | a0001c0001t0001g0033 a0001c0001t0004g0234 a0001c0001t0004g0235 others(44): Show |
64 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.-10-7374C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463248 | |||||||
| chr12:27463656 | G | A | 4 | a0001c0001t0002g0037 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
5 | HG01255.hp2 HG02486.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6966G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463656 | |||||||
| chr12:27463695 | T | C | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-6927T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463695 | |||||||
| chr12:27463815 | G | A | 68 | a0001c0001t0001g0033 a0001c0001t0004g0234 a0001c0001t0004g0235 others(65): Show |
86 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-10-6807G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463815 | |||||||
| chr12:27463844 | A | C | 2 | a0002c0002t0002g0124 a0002c0002t0002g0125 |
2 | NA18979.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-10-6778A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463844 | |||||||
| chr12:27463858 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-10-6764T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27463858 | |||||||
| chr12:27464021 | C | T | 4 | a0003c0004t0006g0015 a0003c0004t0006g0053 a0005c0008t0001g0278 others(1): Show |
5 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-6601C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464021 | |||||||
| chr12:27464066 | C | T | 15 | a0001c0001t0002g0091 a0002c0002t0003g0287 a0002c0002t0004g0034 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-6556C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464066 | |||||||
| chr12:27464175 | G | A | 33 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(30): Show |
46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.-10-6447G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464175 | |||||||
| chr12:27464311 | C | T | 42 | a0001c0001t0001g0033 a0001c0001t0004g0234 a0001c0001t0004g0235 others(39): Show |
57 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-10-6311C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464311 | |||||||
| chr12:27464414 | G | A | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-6208G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464414 | |||||||
| chr12:27464512 | C | T | 5 | a0002c0002t0002g0004 a0002c0002t0002g0068 a0002c0002t0002g0071 others(2): Show |
9 | HG00733.hp2 HG01981.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-10-6110C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464512 | |||||||
| chr12:27464538 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-10-6084G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464538 | |||||||
| chr12:27464610 | G | A | 2 | a0002c0003t0003g0134 a0002c0003t0004g0258 |
2 | HG01884.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-10-6012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464610 | |||||||
| chr12:27464650 | G | A | 4 | a0004c0006t0006g0290 a0004c0006t0006g0291 a0004c0006t0006g0292 others(1): Show |
4 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5972G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464650 | |||||||
| chr12:27464671 | T | A | 1 | a0002c0007t0001g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-5951T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464671 | |||||||
| chr12:27464716 | C | CA | 23 | a0001c0001t0001g0028 a0001c0001t0001g0154 a0001c0001t0001g0159 others(20): Show |
25 | HG00609.hp1 HG00673.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-10-5883dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | C | CAA | 5 | a0002c0002t0002g0106 a0003c0004t0006g0015 a0003c0004t0006g0053 others(2): Show |
6 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5884_-10-5883d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | C | CAAA | 7 | a0001c0001t0001g0173 a0002c0002t0004g0034 a0002c0002t0004g0267 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10-5885_-10-5883d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | C | CAAAA | 7 | a0002c0002t0003g0287 a0002c0002t0004g0245 a0002c0002t0004g0263 others(4): Show |
7 | HG02257.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-5886_-10-5883d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | C | CAAAAAAA others(6): Show |
2 | a0002c0012t0001g0039 a0003c0009t0005g0040 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5895_-10-5883d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0001g0038 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-10-5896_-10-5883d others(16): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464716 | CA | C | 30 | a0001c0001t0001g0156 a0001c0001t0001g0217 a0001c0001t0004g0235 others(27): Show |
40 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-10-5883delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27464716 | ||||||
| chr12:27464717 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-10-5905A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464717 | |||||||
| chr12:27464778 | T | C | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5844T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464778 | |||||||
| chr12:27464787 | C | T | 4 | a0001c0001t0002g0284 a0002c0002t0001g0038 a0002c0012t0001g0039 others(1): Show |
4 | HG02976.hp2 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-5835C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464787 | |||||||
| chr12:27464788 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-10-5834G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464788 | |||||||
| chr12:27464890 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(147): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-10-5732A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27464890 | |||||||
| chr12:27465001 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-10-5621C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465001 | |||||||
| chr12:27465028 | C | CA | 30 | a0001c0001t0001g0024 a0001c0001t0001g0175 a0001c0001t0001g0178 others(27): Show |
34 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-5571dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | ||||||
| chr12:27465028 | CA | C | 31 | a0001c0001t0001g0154 a0001c0001t0001g0172 a0001c0001t0001g0216 others(28): Show |
34 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-10-5571delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | ||||||
| chr12:27465028 | CAAAAAAA others(4): Show |
C | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-5581_-10-5571d others(13): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465028 | ||||||
| chr12:27465044 | A | G | 3 | a0002c0003t0003g0137 a0002c0003t0003g0147 a0002c0003t0003g0148 |
3 | NA18959.hp2 NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-10-5578A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465044 | |||||||
| chr12:27465048 | A | G | 35 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(32): Show |
48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.-10-5574A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465048 | |||||||
| chr12:27465052 | G | A | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5570G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465052 | |||||||
| chr12:27465056 | GA | G | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5562delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465056 | ||||||
| chr12:27465066 | GA | G | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5551delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465066 | ||||||
| chr12:27465070 | AAG | A | 2 | a0001c0001t0001g0033 a0002c0003t0001g0251 |
3 | HG01192.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-10-5538_-10-5537d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27465070 | ||||||
| chr12:27465074 | G | A | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5548G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465074 | |||||||
| chr12:27465076 | G | A | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-5546G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465076 | |||||||
| chr12:27465096 | G | T | 2 | a0002c0003t0003g0143 a0002c0003t0003g0144 |
2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.-10-5526G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465096 | |||||||
| chr12:27465105 | C | G | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-5517C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465105 | |||||||
| chr12:27465379 | C | T | 1 | a0002c0003t0003g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-5243C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465379 | |||||||
| chr12:27465401 | G | A | 1 | a0002c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-5221G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465401 | |||||||
| chr12:27465500 | C | A | 2 | a0002c0002t0002g0107 a0002c0002t0002g0126 |
2 | HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-10-5122C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465500 | |||||||
| chr12:27465541 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0229 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-10-5081G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465541 | |||||||
| chr12:27465864 | C | T | 52 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(49): Show |
66 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.-10-4758C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465864 | |||||||
| chr12:27465998 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(135): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.-10-4624A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27465998 | |||||||
| chr12:27466081 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-4541C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466081 | |||||||
| chr12:27466202 | C | T | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4420C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466202 | |||||||
| chr12:27466219 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-10-4403C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466219 | |||||||
| chr12:27466332 | A | C | 3 | a0002c0002t0002g0020 a0002c0002t0002g0097 a0002c0002t0002g0138 |
4 | NA18959.hp1 NA18966.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-4290A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466332 | |||||||
| chr12:27466390 | C | T | 34 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(31): Show |
47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-4232C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466390 | |||||||
| chr12:27466391 | G | A | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4231G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466391 | |||||||
| chr12:27466395 | G | A | 24 | a0002c0003t0003g0001 a0002c0003t0003g0006 a0002c0003t0003g0011 others(21): Show |
36 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-10-4227G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466395 | |||||||
| chr12:27466612 | G | C | 1 | a0002c0003t0003g0146 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-10-4010G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466612 | |||||||
| chr12:27466791 | A | G | 8 | a0002c0002t0004g0025 a0002c0002t0004g0184 a0002c0003t0004g0258 others(5): Show |
9 | HG01884.hp2 HG02015.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.-10-3831A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466791 | |||||||
| chr12:27466894 | A | G | 37 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(34): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-3728A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27466894 | |||||||
| chr12:27467034 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-10-3588C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467034 | |||||||
| chr12:27467135 | T | A | 2 | a0004c0006t0006g0291 a0004c0006t0006g0293 |
2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-10-3487T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467135 | |||||||
| chr12:27467135 | T | G | 58 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(55): Show |
73 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10-3487T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467135 | |||||||
| chr12:27467277 | A | T | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-3345A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467277 | |||||||
| chr12:27467345 | G | C | 3 | a0002c0002t0001g0038 a0002c0012t0001g0039 a0003c0009t0005g0040 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-10-3277G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467345 | |||||||
| chr12:27467407 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-10-3215A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467407 | |||||||
| chr12:27467657 | G | A | 1 | a0002c0003t0001g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-2965G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467657 | |||||||
| chr12:27467691 | A | G | 1 | a0002c0007t0001g0276 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-10-2931A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467691 | |||||||
| chr12:27467699 | T | C | 1 | a0002c0002t0002g0110 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-10-2923T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467699 | |||||||
| chr12:27467783 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(214): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-10-2839C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467783 | |||||||
| chr12:27467794 | C | T | 60 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(57): Show |
75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2828C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27467794 | |||||||
| chr12:27468037 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-2585T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468037 | |||||||
| chr12:27468053 | A | C | 1 | a0002c0002t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-10-2569A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468053 | |||||||
| chr12:27468115 | G | T | 1 | a0002c0002t0002g0098 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10-2507G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468115 | |||||||
| chr12:27468143 | C | T | 60 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(57): Show |
75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2479C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468143 | |||||||
| chr12:27468154 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-10-2468G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468154 | |||||||
| chr12:27468197 | T | TA | 60 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(57): Show |
75 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10-2424dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27468197 | ||||||
| chr12:27468208 | T | G | 1 | a0002c0003t0003g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-10-2414T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468208 | |||||||
| chr12:27468315 | C | T | 4 | a0002c0003t0003g0001 a0002c0003t0003g0092 a0002c0003t0003g0145 others(1): Show |
10 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-2307C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468315 | |||||||
| chr12:27468386 | CAT | C | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-2234_-10-2233d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27468386 | ||||||
| chr12:27468409 | G | T | 15 | a0002c0002t0003g0287 a0002c0002t0004g0034 a0002c0002t0004g0245 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-2213G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468409 | |||||||
| chr12:27468471 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-10-2151G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468471 | |||||||
| chr12:27468627 | T | C | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1995T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468627 | |||||||
| chr12:27468656 | G | A | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1966G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468656 | |||||||
| chr12:27468677 | G | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0249 |
2 | HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-10-1945G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468677 | |||||||
| chr12:27468684 | G | A | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-1938G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468684 | |||||||
| chr12:27468704 | G | A | 1 | a0001c0001t0002g0017 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-10-1918G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468704 | |||||||
| chr12:27468812 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-10-1810G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468812 | |||||||
| chr12:27468881 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-10-1741A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27468881 | |||||||
| chr12:27469009 | C | T | 37 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(34): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-1613C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469009 | |||||||
| chr12:27469597 | G | A | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1025G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469597 | |||||||
| chr12:27469616 | C | G | 37 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(34): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.-10-1006C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469616 | |||||||
| chr12:27469648 | A | G | 1 | a0002c0003t0003g0137 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-10-974A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469648 | |||||||
| chr12:27469652 | G | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
7 | HG02109.hp1 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-970G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469652 | |||||||
| chr12:27469660 | G | T | 53 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(50): Show |
67 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.-10-962G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469660 | |||||||
| chr12:27469724 | A | G | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-898A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469724 | |||||||
| chr12:27469767 | C | T | 1 | a0002c0003t0003g0132 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-10-855C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469767 | |||||||
| chr12:27469796 | C | T | 34 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(31): Show |
47 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-10-826C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469796 | |||||||
| chr12:27469858 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-10-764C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469858 | |||||||
| chr12:27469915 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-10-707A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27469915 | |||||||
| chr12:27470038 | G | A | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG02647.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-10-584G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470038 | |||||||
| chr12:27470180 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-10-442G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470180 | |||||||
| chr12:27470244 | T | C | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-10-378T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470244 | |||||||
| chr12:27470301 | C | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(214): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-10-321C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470301 | |||||||
| chr12:27470382 | G | A | 62 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(59): Show |
78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10-240G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470382 | |||||||
| chr12:27470383 | C | T | 62 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(59): Show |
78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-10-239C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470383 | |||||||
| chr12:27470388 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-234A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470388 | |||||||
| chr12:27470409 | T | A | 2 | a0001c0001t0002g0093 a0001c0001t0002g0280 |
2 | HG00673.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-10-213T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470409 | |||||||
| chr12:27470438 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-10-184C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | chr12 | 27470438 | |||||||
| chr12:27470500 | G | GT | 213 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(210): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-10-120dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | 27470500 | ||||||
| chr12:27470795 | T | C | 62 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(59): Show |
78 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.134+30T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470795 | |||||||
| chr12:27470818 | G | A | 59 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(56): Show |
75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.134+53G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470818 | |||||||
| chr12:27470883 | A | C | 59 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0243 others(56): Show |
75 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.134+118A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27470883 | |||||||
| chr12:27471124 | C | T | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.134+359C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471124 | |||||||
| chr12:27471179 | T | C | 1 | a0002c0003t0001g0251 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.134+414T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471179 | |||||||
| chr12:27471261 | T | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(163): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.134+496T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471261 | |||||||
| chr12:27471302 | G | A | 1 | a0002c0002t0002g0111 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.134+537G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471302 | |||||||
| chr12:27471431 | C | T | 1 | a0002c0002t0002g0097 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.134+666C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471431 | |||||||
| chr12:27471539 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(196): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.134+774C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471539 | |||||||
| chr12:27471628 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.134+863G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471628 | |||||||
| chr12:27471728 | A | G | 36 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(33): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.134+963A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471728 | |||||||
| chr12:27471952 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(176): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.135-824G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27471952 | |||||||
| chr12:27472009 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(195): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.135-767T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472009 | |||||||
| chr12:27472104 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.135-672A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472104 | |||||||
| chr12:27472158 | G | A | 36 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(33): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.135-618G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472158 | |||||||
| chr12:27472248 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.135-528G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472248 | |||||||
| chr12:27472366 | C | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(198): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.135-410C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472366 | |||||||
| chr12:27472367 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.135-409G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472367 | |||||||
| chr12:27472386 | C | T | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-390C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472386 | |||||||
| chr12:27472490 | C | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.135-286C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472490 | |||||||
| chr12:27472491 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.135-285A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472491 | |||||||
| chr12:27472526 | T | C | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-250T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472526 | |||||||
| chr12:27472529 | G | C | 2 | a0004c0006t0006g0291 a0004c0006t0006g0293 |
2 | HG02735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.135-247G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472529 | |||||||
| chr12:27472624 | A | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0231 a0001c0001t0001g0250 others(1): Show |
4 | HG00639.hp2 HG01192.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-152A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472624 | |||||||
| chr12:27472664 | C | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-112C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472664 | |||||||
| chr12:27472724 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.135-52C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 2/8 | chr12 | 27472724 | |||||||
| chr12:27472890 | A | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.234+15A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472890 | |||||||
| chr12:27472945 | C | T | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.234+70C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472945 | |||||||
| chr12:27472946 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.234+71G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472946 | |||||||
| chr12:27472954 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(199): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.234+79T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27472954 | |||||||
| chr12:27473098 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.234+223C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473098 | |||||||
| chr12:27473245 | G | A | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.234+370G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473245 | |||||||
| chr12:27473357 | C | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.234+482C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473357 | |||||||
| chr12:27473371 | G | C | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+496G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473371 | |||||||
| chr12:27473458 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.234+583C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473458 | |||||||
| chr12:27473569 | C | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+694C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473569 | |||||||
| chr12:27473678 | C | A | 1 | a0001c0001t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234+803C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473678 | |||||||
| chr12:27473698 | A | G | 48 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(45): Show |
64 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.234+823A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473698 | |||||||
| chr12:27473853 | G | T | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-933G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473853 | |||||||
| chr12:27473933 | A | G | 4 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0001g0236 others(1): Show |
4 | HG00639.hp1 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.235-853A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473933 | |||||||
| chr12:27473949 | T | A | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
173 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-837T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473949 | |||||||
| chr12:27473952 | C | T | 1 | a0002c0002t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-834C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473952 | |||||||
| chr12:27473956 | G | T | 1 | a0002c0002t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235-830G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27473956 | |||||||
| chr12:27474114 | C | G | 133 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(130): Show |
170 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.235-672C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474114 | |||||||
| chr12:27474220 | C | T | 1 | a0002c0003t0003g0144 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.235-566C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474220 | |||||||
| chr12:27474227 | A | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.235-559A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474227 | |||||||
| chr12:27474536 | G | A | 44 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(41): Show |
60 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.235-250G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474536 | |||||||
| chr12:27474567 | G | A | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-219G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474567 | |||||||
| chr12:27474604 | T | C | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
173 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.235-182T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474604 | |||||||
| chr12:27474608 | C | T | 6 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(3): Show |
7 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.235-178C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474608 | |||||||
| chr12:27474626 | A | G | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
10 | HG01192.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.235-160A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474626 | |||||||
| chr12:27474634 | T | C | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.235-152T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474634 | |||||||
| chr12:27474743 | C | G | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.235-43C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 3/8 | chr12 | 27474743 | |||||||
| chr12:27474914 | G | A | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | splice_donor_variant&intron_variant | HIGH | c.362+1G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27474914 | |||||||
| chr12:27475101 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.362+188G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475101 | |||||||
| chr12:27475172 | G | A | 133 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(130): Show |
170 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.362+259G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475172 | |||||||
| chr12:27475195 | T | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.362+282T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475195 | |||||||
| chr12:27475243 | C | A | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.362+330C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475243 | |||||||
| chr12:27475260 | T | G | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.363-322T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475260 | |||||||
| chr12:27475360 | A | T | 3 | a0002c0003t0003g0022 a0002c0003t0003g0146 a0002c0003t0003g0152 |
4 | HG03239.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.363-222A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475360 | |||||||
| chr12:27475379 | A | G | 1 | a0002c0003t0003g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.363-203A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475379 | |||||||
| chr12:27475399 | C | T | 130 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(127): Show |
167 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.363-183C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 4/8 | chr12 | 27475399 | |||||||
| chr12:27475809 | T | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(114): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.512+78T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27475809 | |||||||
| chr12:27476250 | A | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.512+519A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476250 | |||||||
| chr12:27476262 | T | G | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+531T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476262 | |||||||
| chr12:27476471 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.512+740A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476471 | |||||||
| chr12:27476812 | A | G | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1081A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476812 | |||||||
| chr12:27476893 | C | A | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1162C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476893 | |||||||
| chr12:27476970 | T | C | 4 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(1): Show |
5 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.512+1239T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476970 | |||||||
| chr12:27476986 | T | C | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1255T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27476986 | |||||||
| chr12:27477000 | T | A | 3 | a0002c0002t0002g0005 a0002c0002t0002g0108 a0002c0002t0002g0110 |
7 | NA18977.hp2 NA18985.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.512+1269T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477000 | |||||||
| chr12:27477120 | A | G | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1389A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477120 | |||||||
| chr12:27477167 | G | T | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1436G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477167 | |||||||
| chr12:27477182 | T | A | 1 | a0002c0002t0003g0287 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.512+1451T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477182 | |||||||
| chr12:27477209 | GGTTTT | G | 10 | a0002c0003t0003g0142 a0002c0003t0003g0148 a0003c0004t0005g0023 others(7): Show |
12 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.512+1479_512+1483d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTT | G | 35 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(32): Show |
49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.512+1479_512+1484d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT | G | 3 | a0002c0003t0003g0137 a0002c0003t0003g0149 a0002c0007t0001g0274 |
3 | HG02257.hp1 NA18959.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.512+1479_512+1485d others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT others(1): Show |
G | 3 | a0002c0002t0001g0048 a0002c0002t0001g0051 a0002c0002t0001g0052 |
3 | HG02055.hp2 HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.512+1479_512+1486d others(10): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT others(2): Show |
G | 10 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(7): Show |
10 | HG00544.hp1 HG00741.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.512+1479_512+1487d others(11): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT others(3): Show |
G | 52 | a0002c0002t0001g0221 a0002c0002t0002g0002 a0002c0002t0002g0004 others(49): Show |
72 | HG00558.hp2 HG00733.hp2 HG01168.hp1 others(69): Show |
intron_variant | MODIFIER | c.512+1479_512+1488d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT others(4): Show |
G | 1 | a0002c0002t0002g0124 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.512+1479_512+1489d others(13): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477209 | GGTTTTTT others(6): Show |
G | 15 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+1479_512+1491d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477209 | |||||||
| chr12:27477210 | G | GT | 37 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.512+1504dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | ||||||
| chr12:27477210 | G | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+1479G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477210 | |||||||
| chr12:27477210 | GT | G | 29 | a0001c0001t0001g0160 a0001c0001t0001g0168 a0001c0001t0001g0170 others(26): Show |
31 | HG00438.hp1 HG00544.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.512+1504delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | ||||||
| chr12:27477210 | GTT | G | 5 | a0001c0001t0002g0016 a0001c0001t0002g0037 a0001c0001t0002g0055 others(2): Show |
6 | HG01255.hp2 HG03491.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+1503_512+1504d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | ||||||
| chr12:27477210 | GTTTTTTT others(3): Show |
G | 1 | a0002c0002t0002g0113 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.512+1495_512+1504d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | ||||||
| chr12:27477210 | GTTTTTTT others(6): Show |
G | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+1492_512+1504d others(15): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477210 | ||||||
| chr12:27477273 | T | TTGCC | 8 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(5): Show |
8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+1544_512+1547d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477273 | ||||||
| chr12:27477331 | T | C | 1 | a0002c0002t0002g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.512+1600T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477331 | |||||||
| chr12:27477405 | G | A | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1674G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477405 | |||||||
| chr12:27477431 | C | A | 1 | a0001c0001t0004g0234 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.512+1700C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477431 | |||||||
| chr12:27477438 | A | C | 48 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(45): Show |
64 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.512+1707A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477438 | |||||||
| chr12:27477496 | G | T | 2 | a0002c0002t0002g0101 a0002c0002t0002g0102 |
2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.512+1765G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477496 | |||||||
| chr12:27477576 | A | AT | 270 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(267): Show |
334 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.512+1847dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477576 | ||||||
| chr12:27477617 | CTTCATTC others(3): Show |
C | 1 | a0001c0001t0002g0085 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.512+1899_512+1908d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477617 | ||||||
| chr12:27477634 | C | CT | 26 | a0001c0001t0001g0036 a0001c0001t0001g0156 a0001c0001t0001g0157 others(23): Show |
27 | HG00280.hp2 HG00738.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.512+1919dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTT | 74 | a0001c0001t0001g0168 a0002c0002t0001g0038 a0002c0002t0001g0041 others(71): Show |
95 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.512+1918_512+1919d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTTTTT | 8 | a0002c0003t0003g0144 a0003c0004t0005g0023 a0003c0004t0005g0032 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.512+1915_512+1919d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTTTTTT | 33 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(30): Show |
46 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.512+1914_512+1919d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTTTTTTT | 7 | a0002c0003t0001g0251 a0002c0003t0003g0022 a0002c0003t0003g0130 others(4): Show |
8 | HG02080.hp1 HG03239.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.512+1913_512+1919d others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTTTTTTT others(3): Show |
1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+1910_512+1919d others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | CTTTTTTT others(18): Show |
2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+1919_512+1920i others(27): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477634 | ||||||
| chr12:27477634 | C | T | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+1903C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477634 | |||||||
| chr12:27477722 | TTA | T | 11 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+1993_512+1994d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27477722 | ||||||
| chr12:27477728 | C | A | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+1997C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477728 | |||||||
| chr12:27477775 | A | G | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+2044A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477775 | |||||||
| chr12:27477804 | T | A | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.512+2073T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477804 | |||||||
| chr12:27477868 | T | A | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2137T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477868 | |||||||
| chr12:27477903 | G | T | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2172G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477903 | |||||||
| chr12:27477943 | C | T | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2212C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477943 | |||||||
| chr12:27477982 | T | C | 9 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(6): Show |
9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+2251T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27477982 | |||||||
| chr12:27478058 | G | C | 1 | a0002c0003t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.512+2327G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478058 | |||||||
| chr12:27478103 | A | G | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.512+2372A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478103 | |||||||
| chr12:27478153 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+2422C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478153 | |||||||
| chr12:27478162 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.512+2431A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478162 | |||||||
| chr12:27478183 | G | A | 25 | a0002c0003t0003g0001 a0002c0003t0003g0006 a0002c0003t0003g0011 others(22): Show |
37 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.512+2452G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478183 | |||||||
| chr12:27478195 | T | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+2464T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478195 | |||||||
| chr12:27478269 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.512+2538A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478269 | |||||||
| chr12:27478368 | T | C | 36 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(33): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.512+2637T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478368 | |||||||
| chr12:27478447 | A | C | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2716A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478447 | |||||||
| chr12:27478537 | C | T | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+2806C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478537 | |||||||
| chr12:27478615 | C | T | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+2884C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478615 | |||||||
| chr12:27478651 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+2920C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478651 | |||||||
| chr12:27478736 | A | G | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.512+3005A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478736 | |||||||
| chr12:27478764 | A | G | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.512+3033A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478764 | |||||||
| chr12:27478777 | A | ACCAG | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3048_512+3049i others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27478777 | ||||||
| chr12:27478780 | C | A | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3049C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478780 | |||||||
| chr12:27478783 | A | AC | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3052_512+3053i others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478783 | |||||||
| chr12:27478847 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0216 |
2 | HG01106.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.512+3116C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478847 | |||||||
| chr12:27478907 | T | C | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.512+3176T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478907 | |||||||
| chr12:27478912 | G | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3181G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27478912 | |||||||
| chr12:27479221 | T | C | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.512+3490T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479221 | |||||||
| chr12:27479253 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3522C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479253 | |||||||
| chr12:27479255 | T | G | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3524T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479255 | |||||||
| chr12:27479341 | G | C | 2 | a0002c0003t0003g0150 a0002c0003t0003g0151 |
2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.512+3610G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479341 | |||||||
| chr12:27479347 | C | T | 15 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+3616C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479347 | |||||||
| chr12:27479349 | G | A | 15 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.512+3618G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479349 | |||||||
| chr12:27479402 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.512+3671G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479402 | |||||||
| chr12:27479466 | G | C | 1 | a0003c0004t0005g0257 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.512+3735G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479466 | |||||||
| chr12:27479482 | T | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3751T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479482 | |||||||
| chr12:27479508 | G | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3777G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479508 | |||||||
| chr12:27479544 | TATG | T | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.512+3818_512+3820d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27479544 | ||||||
| chr12:27479557 | T | C | 9 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(6): Show |
9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+3826T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479557 | |||||||
| chr12:27479619 | G | A | 1 | a0002c0003t0004g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.512+3888G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479619 | |||||||
| chr12:27479646 | G | T | 60 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(57): Show |
80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.512+3915G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479646 | |||||||
| chr12:27479651 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3920C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479651 | |||||||
| chr12:27479666 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0286 |
3 | HG02486.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.512+3935G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479666 | |||||||
| chr12:27479695 | A | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+3964A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479695 | |||||||
| chr12:27479719 | G | A | 75 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(72): Show |
96 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.512+3988G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479719 | |||||||
| chr12:27479753 | C | T | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+4022C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479753 | |||||||
| chr12:27479777 | A | G | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4046A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479777 | |||||||
| chr12:27479866 | A | T | 9 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(6): Show |
9 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.512+4135A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479866 | |||||||
| chr12:27479884 | C | CAT | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4154_512+4155i others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27479884 | ||||||
| chr12:27479886 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4155C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479886 | |||||||
| chr12:27479887 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0002g0037 |
4 | HG01192.hp1 HG02717.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.512+4156G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479887 | |||||||
| chr12:27479909 | T | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4178T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479909 | |||||||
| chr12:27479941 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4210C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27479941 | |||||||
| chr12:27480027 | A | C | 2 | a0002c0003t0004g0161 a0002c0003t0004g0233 |
2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.512+4296A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480027 | |||||||
| chr12:27480119 | A | T | 1 | a0001c0001t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.512+4388A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480119 | |||||||
| chr12:27480324 | T | C | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4593T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480324 | |||||||
| chr12:27480357 | T | A | 11 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.512+4626T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480357 | |||||||
| chr12:27480379 | G | T | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.512+4648G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480379 | |||||||
| chr12:27480424 | C | T | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+4693C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480424 | |||||||
| chr12:27480448 | C | A | 1 | a0001c0001t0002g0056 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.512+4717C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480448 | |||||||
| chr12:27480462 | G | C | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG00738.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.512+4731G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480462 | |||||||
| chr12:27480707 | C | G | 6 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0001g0197 others(3): Show |
6 | HG00099.hp1 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.512+4976C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480707 | |||||||
| chr12:27480708 | C | T | 137 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(134): Show |
175 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.512+4977C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480708 | |||||||
| chr12:27480709 | CT | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0217 a0001c0001t0001g0247 others(4): Show |
7 | HG02572.hp2 HG02647.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.512+4979delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480709 | |||||||
| chr12:27480930 | T | C | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5199T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27480930 | |||||||
| chr12:27481092 | G | C | 1 | a0002c0003t0001g0222 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.512+5361G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481092 | |||||||
| chr12:27481173 | T | C | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+5442T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481173 | |||||||
| chr12:27481277 | A | G | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5546A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481277 | |||||||
| chr12:27481310 | G | A | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5579G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481310 | |||||||
| chr12:27481325 | G | A | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5594G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481325 | |||||||
| chr12:27481348 | C | T | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+5617C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481348 | |||||||
| chr12:27481449 | A | G | 49 | a0002c0002t0001g0221 a0002c0002t0002g0002 a0002c0002t0002g0004 others(46): Show |
69 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.512+5718A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481449 | |||||||
| chr12:27481462 | A | G | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.512+5731A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481462 | |||||||
| chr12:27481471 | T | C | 61 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(58): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.512+5740T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481471 | |||||||
| chr12:27481674 | C | A | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.512+5943C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481674 | |||||||
| chr12:27481794 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.512+6063G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481794 | |||||||
| chr12:27481810 | A | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.512+6079A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481810 | |||||||
| chr12:27481841 | T | C | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+6110T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481841 | |||||||
| chr12:27481871 | T | G | 2 | a0005c0008t0001g0278 a0005c0008t0001g0279 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.512+6140T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27481871 | |||||||
| chr12:27482009 | C | CTT | 84 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(81): Show |
105 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(102): Show |
intron_variant | MODIFIER | c.512+6288_512+6289d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27482009 | ||||||
| chr12:27482093 | A | G | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.512+6362A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482093 | |||||||
| chr12:27482171 | T | A | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-6289T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482171 | |||||||
| chr12:27482267 | T | C | 8 | a0002c0003t0003g0011 a0002c0003t0003g0035 a0002c0003t0003g0129 others(5): Show |
11 | NA18940.hp2 NA18945.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-6193T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482267 | |||||||
| chr12:27482283 | C | A | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-6177C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482283 | |||||||
| chr12:27482341 | G | T | 1 | a0002c0003t0004g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513-6119G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482341 | |||||||
| chr12:27482551 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.513-5909T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482551 | |||||||
| chr12:27482662 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0001g0236 others(1): Show |
4 | HG00639.hp1 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-5798G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482662 | |||||||
| chr12:27482831 | A | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-5629A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482831 | |||||||
| chr12:27482846 | T | C | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-5614T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482846 | |||||||
| chr12:27482848 | T | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-5612T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27482848 | |||||||
| chr12:27483068 | A | T | 10 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(7): Show |
10 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-5392A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483068 | |||||||
| chr12:27483200 | G | A | 10 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(7): Show |
10 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-5260G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483200 | |||||||
| chr12:27483242 | A | C | 80 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(77): Show |
101 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(98): Show |
intron_variant | MODIFIER | c.513-5218A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483242 | |||||||
| chr12:27483378 | C | T | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-5082C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483378 | |||||||
| chr12:27483385 | C | G | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.513-5075C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483385 | |||||||
| chr12:27483497 | A | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-4963A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483497 | |||||||
| chr12:27483574 | A | T | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-4886A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483574 | |||||||
| chr12:27483704 | C | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-4756C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483704 | |||||||
| chr12:27483705 | G | A | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-4755G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483705 | |||||||
| chr12:27483803 | A | C | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-4657A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483803 | |||||||
| chr12:27483901 | A | G | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-4559A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27483901 | |||||||
| chr12:27484007 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.513-4453C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484007 | |||||||
| chr12:27484011 | TTTACTA | T | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-4444_513-4439d others(8): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484011 | ||||||
| chr12:27484195 | A | G | 79 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(76): Show |
100 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.513-4265A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484195 | |||||||
| chr12:27484216 | C | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0238 |
2 | HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.513-4244C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484216 | |||||||
| chr12:27484236 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.513-4224C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484236 | |||||||
| chr12:27484275 | A | T | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-4185A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484275 | |||||||
| chr12:27484328 | A | G | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.513-4132A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484328 | |||||||
| chr12:27484783 | G | T | 2 | a0002c0003t0003g0143 a0002c0003t0003g0144 |
2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.513-3677G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484783 | |||||||
| chr12:27484809 | T | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3651T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484809 | |||||||
| chr12:27484831 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3629G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484831 | |||||||
| chr12:27484839 | A | G | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-3621A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484839 | |||||||
| chr12:27484847 | A | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3613A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484847 | |||||||
| chr12:27484851 | CA | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(75): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.513-3588delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | ||||||
| chr12:27484851 | CAA | C | 13 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0168 others(10): Show |
16 | HG01175.hp1 HG01361.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.513-3589_513-3588d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | ||||||
| chr12:27484851 | CAAA | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0249 others(11): Show |
17 | HG00280.hp1 HG01069.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.513-3590_513-3588d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484851 | ||||||
| chr12:27484862 | AAAAAAAA others(10): Show |
A | 60 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(57): Show |
80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.513-3596_513-3580d others(19): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484862 | ||||||
| chr12:27484863 | AAAAAAAA others(7): Show |
A | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-3595_513-3582d others(16): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484863 | ||||||
| chr12:27484863 | AAAAAAAA others(9): Show |
A | 22 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(19): Show |
23 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.513-3595_513-3580d others(18): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484863 | ||||||
| chr12:27484869 | A | T | 2 | a0001c0001t0001g0007 a0001c0005t0002g0063 |
2 | HG01069.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.513-3591A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484869 | |||||||
| chr12:27484870 | AAAT | A | 12 | a0001c0001t0002g0017 a0001c0001t0002g0019 a0001c0001t0002g0069 others(9): Show |
14 | HG00544.hp2 HG02015.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.513-3588_513-3586d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484870 | ||||||
| chr12:27484871 | A | AT | 10 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0001g0179 others(7): Show |
10 | HG00099.hp1 HG00673.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-3589_513-3588i others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484871 | |||||||
| chr12:27484871 | A | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(30): Show |
37 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.513-3589A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484871 | |||||||
| chr12:27484871 | AAT | A | 38 | a0001c0001t0001g0158 a0001c0001t0001g0190 a0001c0001t0001g0200 others(35): Show |
48 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.513-3567_513-3566d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27484871 | ||||||
| chr12:27484872 | AT | A | 9 | a0001c0001t0001g0155 a0001c0001t0001g0193 a0001c0001t0002g0018 others(6): Show |
10 | HG00673.hp1 HG01258.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.513-3587delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484872 | |||||||
| chr12:27484872 | ATAT | A | 10 | a0002c0003t0001g0186 a0002c0003t0001g0189 a0002c0003t0003g0001 others(7): Show |
10 | HG00438.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.513-3587_513-3585d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484872 | |||||||
| chr12:27484873 | T | A | 1 | a0001c0001t0001g0012 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.513-3587T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484873 | |||||||
| chr12:27484875 | T | A | 32 | a0002c0003t0001g0027 a0002c0003t0001g0211 a0002c0003t0003g0001 others(29): Show |
42 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.513-3585T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484875 | |||||||
| chr12:27484877 | T | A | 3 | a0002c0003t0003g0001 a0002c0003t0003g0130 a0002c0003t0003g0141 |
3 | HG02004.hp1 HG02080.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.513-3583T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484877 | |||||||
| chr12:27484880 | A | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-3580A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484880 | |||||||
| chr12:27484882 | A | G | 82 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(79): Show |
103 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(100): Show |
intron_variant | MODIFIER | c.513-3578A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484882 | |||||||
| chr12:27484888 | A | G | 1 | a0002c0003t0001g0211 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.513-3572A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484888 | |||||||
| chr12:27484921 | C | A | 1 | a0001c0001t0001g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.513-3539C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484921 | |||||||
| chr12:27484935 | T | C | 1 | a0002c0002t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.513-3525T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484935 | |||||||
| chr12:27484949 | T | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3511T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484949 | |||||||
| chr12:27484959 | G | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3501G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27484959 | |||||||
| chr12:27485074 | T | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3386T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485074 | |||||||
| chr12:27485131 | T | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3329T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485131 | |||||||
| chr12:27485141 | T | TCTAA | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3317_513-3316i others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485141 | ||||||
| chr12:27485310 | T | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-3150T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485310 | |||||||
| chr12:27485323 | C | T | 5 | a0002c0003t0003g0137 a0002c0003t0003g0143 a0002c0003t0003g0144 others(2): Show |
5 | NA18939.hp1 NA18959.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.513-3137C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485323 | |||||||
| chr12:27485450 | G | GCT | 16 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(13): Show |
17 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-3010_513-3009i others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485450 | |||||||
| chr12:27485450 | G | GT | 16 | a0001c0001t0001g0033 a0001c0001t0001g0175 a0001c0001t0001g0176 others(13): Show |
17 | HG00609.hp1 HG00738.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.513-2993dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | ||||||
| chr12:27485450 | G | GTT | 8 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(5): Show |
8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-2994_513-2993d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | ||||||
| chr12:27485450 | GT | G | 55 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0002g0037 others(52): Show |
72 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.513-2993delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27485450 | ||||||
| chr12:27485511 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.513-2949G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485511 | |||||||
| chr12:27485555 | T | C | 1 | a0002c0003t0001g0186 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.513-2905T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485555 | |||||||
| chr12:27485604 | T | C | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.513-2856T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485604 | |||||||
| chr12:27485606 | A | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2854A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485606 | |||||||
| chr12:27485607 | T | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2853T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485607 | |||||||
| chr12:27485617 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.513-2843T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485617 | |||||||
| chr12:27485895 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2565G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485895 | |||||||
| chr12:27485971 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.513-2489C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485971 | |||||||
| chr12:27485974 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.513-2486C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27485974 | |||||||
| chr12:27486051 | T | C | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-2409T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486051 | |||||||
| chr12:27486096 | T | C | 11 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(8): Show |
11 | HG00741.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.513-2364T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486096 | |||||||
| chr12:27486131 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.513-2329T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486131 | |||||||
| chr12:27486162 | C | A | 1 | a0001c0005t0002g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.513-2298C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486162 | |||||||
| chr12:27486388 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513-2072C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486388 | |||||||
| chr12:27486448 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.513-2012C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486448 | |||||||
| chr12:27486619 | G | T | 3 | a0002c0002t0002g0074 a0002c0002t0002g0075 a0002c0002t0002g0088 |
3 | HG02071.hp2 HG02074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.513-1841G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486619 | |||||||
| chr12:27486671 | T | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1789T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486671 | |||||||
| chr12:27486693 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.513-1767A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486693 | |||||||
| chr12:27486758 | G | A | 1 | a0002c0002t0002g0128 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.513-1702G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486758 | |||||||
| chr12:27486816 | C | T | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1644C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486816 | |||||||
| chr12:27486825 | A | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1635A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486825 | |||||||
| chr12:27486959 | A | C | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.513-1501A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486959 | |||||||
| chr12:27486971 | G | T | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-1489G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27486971 | |||||||
| chr12:27487087 | C | T | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-1373C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487087 | |||||||
| chr12:27487123 | C | A | 1 | a0002c0002t0002g0110 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.513-1337C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487123 | |||||||
| chr12:27487144 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.513-1316T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487144 | |||||||
| chr12:27487246 | C | T | 1 | a0002c0002t0002g0100 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513-1214C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487246 | |||||||
| chr12:27487343 | C | CT | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1110dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487343 | ||||||
| chr12:27487352 | A | C | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.513-1108A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487352 | |||||||
| chr12:27487388 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.513-1072C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487388 | |||||||
| chr12:27487418 | T | C | 1 | a0002c0003t0003g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.513-1042T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487418 | |||||||
| chr12:27487424 | GTAGTCTT others(9): Show |
G | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.513-1035_513-1020d others(18): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487424 | |||||||
| chr12:27487440 | T | G | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-1020T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487440 | |||||||
| chr12:27487535 | C | T | 4 | a0001c0001t0001g0246 a0002c0002t0001g0038 a0002c0002t0004g0266 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.513-925C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487535 | |||||||
| chr12:27487537 | C | T | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-923C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487537 | |||||||
| chr12:27487538 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-922G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487538 | |||||||
| chr12:27487629 | G | A | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-831G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487629 | |||||||
| chr12:27487635 | G | A | 2 | a0002c0003t0001g0186 a0002c0003t0001g0189 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.513-825G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487635 | |||||||
| chr12:27487698 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0002g0073 |
2 | HG03041.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.513-762G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487698 | |||||||
| chr12:27487699 | C | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.513-761C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487699 | |||||||
| chr12:27487753 | C | CT | 8 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 others(5): Show |
8 | HG02015.hp2 HG02735.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.513-691dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | ||||||
| chr12:27487753 | C | CTT | 15 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.513-692_513-691dup others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | ||||||
| chr12:27487753 | CT | C | 52 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(49): Show |
68 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.513-691delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487753 | ||||||
| chr12:27487772 | C | G | 1 | a0001c0001t0002g0091 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.513-688C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487772 | |||||||
| chr12:27487877 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.513-583T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487877 | |||||||
| chr12:27487941 | T | A | 1 | a0002c0002t0002g0115 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.513-519T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27487941 | |||||||
| chr12:27487941 | T | TA | 85 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(82): Show |
106 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(103): Show |
intron_variant | MODIFIER | c.513-517dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr12 | 27487941 | ||||||
| chr12:27488001 | G | A | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.513-459G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488001 | |||||||
| chr12:27488017 | T | G | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.513-443T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488017 | |||||||
| chr12:27488061 | T | C | 1 | a0003c0013t0006g0050 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.513-399T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488061 | |||||||
| chr12:27488133 | T | A | 1 | a0001c0001t0002g0121 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.513-327T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488133 | |||||||
| chr12:27488155 | C | T | 2 | a0002c0002t0004g0025 a0002c0002t0004g0184 |
3 | HG02602.hp2 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.513-305C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488155 | |||||||
| chr12:27488278 | T | C | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.513-182T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488278 | |||||||
| chr12:27488413 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.513-47G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488413 | |||||||
| chr12:27488442 | A | G | 78 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(75): Show |
99 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.513-18A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 5/8 | chr12 | 27488442 | |||||||
| chr12:27488641 | G | A | 2 | a0002c0003t0004g0161 a0002c0003t0004g0233 |
2 | NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.600+94G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488641 | |||||||
| chr12:27488753 | A | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+206A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488753 | |||||||
| chr12:27488769 | C | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+222C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488769 | |||||||
| chr12:27488784 | T | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+237T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488784 | |||||||
| chr12:27488801 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+254G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488801 | |||||||
| chr12:27488819 | G | C | 1 | a0007c0010t0001g0232 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.600+272G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488819 | |||||||
| chr12:27488851 | C | T | 61 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(58): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+304C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488851 | |||||||
| chr12:27488895 | G | C | 1 | a0002c0002t0002g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.600+348G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488895 | |||||||
| chr12:27488957 | T | G | 35 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(32): Show |
49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.600+410T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27488957 | |||||||
| chr12:27489024 | T | C | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.600+477T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489024 | |||||||
| chr12:27489142 | G | A | 1 | a0001c0001t0002g0284 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+595G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489142 | |||||||
| chr12:27489145 | T | A | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+598T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489145 | |||||||
| chr12:27489190 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+643G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489190 | |||||||
| chr12:27489296 | A | G | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.600+749A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489296 | |||||||
| chr12:27489302 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.600+755G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489302 | |||||||
| chr12:27489339 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+792G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489339 | |||||||
| chr12:27489461 | A | G | 61 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(58): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.600+914A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489461 | |||||||
| chr12:27489602 | G | A | 6 | a0003c0013t0006g0050 a0004c0006t0006g0214 a0004c0006t0006g0290 others(3): Show |
6 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+1055G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489602 | |||||||
| chr12:27489605 | A | G | 3 | a0002c0012t0001g0039 a0003c0009t0005g0040 a0003c0009t0005g0044 |
3 | HG02976.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.600+1058A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489605 | |||||||
| chr12:27489609 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1062G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27489609 | |||||||
| chr12:27490078 | C | A | 2 | a0002c0002t0002g0109 a0002c0002t0002g0116 |
2 | HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.600+1531C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490078 | |||||||
| chr12:27490149 | C | T | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1602C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490149 | |||||||
| chr12:27490250 | G | A | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.600+1703G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490250 | |||||||
| chr12:27490269 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1722G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490269 | |||||||
| chr12:27490306 | C | T | 60 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(57): Show |
80 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.600+1759C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490306 | |||||||
| chr12:27490506 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1959G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490506 | |||||||
| chr12:27490514 | A | G | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+1967A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490514 | |||||||
| chr12:27490673 | T | G | 1 | a0002c0002t0002g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.600+2126T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490673 | |||||||
| chr12:27490678 | C | T | 2 | a0002c0002t0002g0106 a0002c0002t0002g0127 |
2 | HG02683.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.600+2131C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490678 | |||||||
| chr12:27490718 | T | C | 135 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(132): Show |
172 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(169): Show |
intron_variant | MODIFIER | c.600+2171T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490718 | |||||||
| chr12:27490720 | C | T | 4 | a0002c0007t0001g0215 a0002c0007t0001g0274 a0002c0007t0001g0275 others(1): Show |
4 | HG01884.hp1 HG02257.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2173C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490720 | |||||||
| chr12:27490741 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2194G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490741 | |||||||
| chr12:27490852 | C | A | 1 | a0001c0001t0002g0280 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.600+2305C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27490852 | |||||||
| chr12:27491094 | G | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2547G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491094 | |||||||
| chr12:27491162 | C | T | 1 | a0002c0002t0002g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.600+2615C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491162 | |||||||
| chr12:27491261 | G | T | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2714G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491261 | |||||||
| chr12:27491353 | ATAG | A | 87 | a0002c0002t0001g0038 a0002c0002t0001g0041 a0002c0002t0001g0042 others(84): Show |
108 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.600+2807_600+2809d others(5): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491353 | |||||||
| chr12:27491426 | G | A | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-2874G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491426 | |||||||
| chr12:27491562 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.601-2738C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491562 | |||||||
| chr12:27491573 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.601-2727C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491573 | |||||||
| chr12:27491705 | T | G | 44 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(41): Show |
60 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.601-2595T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491705 | |||||||
| chr12:27491710 | C | CT | 39 | a0002c0003t0001g0251 a0002c0003t0003g0001 a0002c0003t0003g0006 others(36): Show |
53 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.601-2577dupT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27491710 | ||||||
| chr12:27491710 | C | CTT | 9 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(6): Show |
11 | HG00642.hp2 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.601-2578_601-2577d others(4): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27491710 | ||||||
| chr12:27491947 | C | T | 2 | a0001c0001t0002g0069 a0001c0001t0002g0077 |
2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.601-2353C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491947 | |||||||
| chr12:27491978 | G | T | 17 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.601-2322G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27491978 | |||||||
| chr12:27492068 | T | C | 61 | a0002c0002t0001g0041 a0002c0002t0001g0042 a0002c0002t0001g0043 others(58): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.601-2232T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492068 | |||||||
| chr12:27492099 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.601-2201G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492099 | |||||||
| chr12:27492139 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.601-2161A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492139 | |||||||
| chr12:27492149 | T | G | 36 | a0002c0003t0001g0027 a0002c0003t0001g0186 a0002c0003t0001g0189 others(33): Show |
50 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.601-2151T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492149 | |||||||
| chr12:27492209 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-2091A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492209 | |||||||
| chr12:27492258 | T | C | 2 | a0002c0002t0001g0045 a0002c0002t0001g0048 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.601-2042T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492258 | |||||||
| chr12:27492276 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.601-2024G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492276 | |||||||
| chr12:27492311 | T | G | 17 | a0002c0002t0001g0038 a0002c0002t0003g0287 a0002c0002t0004g0034 others(14): Show |
18 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.601-1989T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492311 | |||||||
| chr12:27492456 | G | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-1844G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492456 | |||||||
| chr12:27492743 | A | G | 8 | a0002c0002t0001g0038 a0002c0002t0004g0034 a0002c0002t0004g0266 others(5): Show |
9 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-1557A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492743 | |||||||
| chr12:27492780 | C | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0001g0197 |
3 | HG00099.hp1 HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.601-1520C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492780 | |||||||
| chr12:27492945 | A | G | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.601-1355A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27492945 | |||||||
| chr12:27493014 | G | A | 8 | a0002c0003t0003g0149 a0003c0004t0005g0023 a0003c0004t0005g0032 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-1286G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493014 | |||||||
| chr12:27493035 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.601-1265A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493035 | |||||||
| chr12:27493116 | G | A | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-1184G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493116 | |||||||
| chr12:27493132 | G | T | 45 | a0001c0001t0001g0281 a0001c0001t0002g0288 a0002c0003t0001g0186 others(42): Show |
61 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.601-1168G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493132 | |||||||
| chr12:27493187 | G | A | 5 | a0004c0006t0006g0214 a0004c0006t0006g0290 a0004c0006t0006g0291 others(2): Show |
5 | HG02015.hp2 HG02735.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-1113G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493187 | |||||||
| chr12:27493251 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.601-1049T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493251 | |||||||
| chr12:27493282 | A | G | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-1018A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493282 | |||||||
| chr12:27493298 | G | A | 65 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0002t0001g0038 others(62): Show |
82 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.601-1002G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493298 | |||||||
| chr12:27493339 | A | T | 8 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-961A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493339 | |||||||
| chr12:27493417 | A | G | 2 | a0001c0001t0001g0281 a0001c0001t0002g0288 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-883A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493417 | |||||||
| chr12:27493532 | CA | C | 51 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0204 others(48): Show |
66 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.601-756delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr12 | 27493532 | ||||||
| chr12:27493548 | A | T | 43 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0003t0001g0027 others(40): Show |
58 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.601-752A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493548 | |||||||
| chr12:27493604 | T | C | 3 | a0001c0001t0002g0016 a0001c0001t0002g0055 a0001c0001t0002g0060 |
4 | HG01975.hp2 NA18950.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-696T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493604 | |||||||
| chr12:27493697 | G | C | 2 | a0001c0001t0001g0281 a0001c0001t0002g0288 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-603G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493697 | |||||||
| chr12:27493793 | C | T | 112 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0239 others(109): Show |
150 | HG00099.hp2 HG00438.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.601-507C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493793 | |||||||
| chr12:27493971 | T | G | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.601-329T>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493971 | |||||||
| chr12:27493996 | T | A | 2 | a0003c0004t0006g0015 a0003c0004t0006g0053 |
3 | HG00099.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.601-304T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27493996 | |||||||
| chr12:27494076 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.601-224A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494076 | |||||||
| chr12:27494261 | T | C | 1 | a0002c0002t0004g0245 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-39T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494261 | |||||||
| chr12:27494276 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0248 others(2): Show |
5 | HG02572.hp2 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-24C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 6/8 | chr12 | 27494276 | |||||||
| chr12:27494449 | C | T | 18 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(15): Show |
21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+93C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494449 | |||||||
| chr12:27494487 | T | TTTA | 26 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0190 others(23): Show |
29 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.657+166_657+168dup others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | T | TTTATTA | 61 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0012 others(58): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.657+163_657+168dup others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | T | TTTATTAT others(2): Show |
48 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(45): Show |
53 | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.657+160_657+168dup others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | T | TTTATTAT others(5): Show |
1 | a0001c0001t0001g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.657+157_657+168dup others(12): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | TTTA | T | 18 | a0001c0001t0001g0014 a0001c0001t0001g0169 a0001c0001t0001g0170 others(15): Show |
21 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+166_657+168del others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | TTTATTA | T | 68 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(65): Show |
91 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.657+163_657+168del others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494487 | TTTATTAT others(2): Show |
T | 34 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0003t0001g0027 others(31): Show |
48 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.657+160_657+168del others(9): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr12 | 27494487 | ||||||
| chr12:27494544 | A | C | 6 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(3): Show |
6 | HG00741.hp2 HG02886.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.657+188A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494544 | |||||||
| chr12:27494744 | T | A | 18 | a0003c0004t0005g0023 a0003c0004t0005g0032 a0003c0004t0005g0252 others(15): Show |
21 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.657+388T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27494744 | |||||||
| chr12:27495023 | T | A | 2 | a0002c0007t0001g0215 a0002c0007t0001g0276 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.658-657T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495023 | |||||||
| chr12:27495192 | G | A | 6 | a0001c0001t0001g0231 a0001c0001t0001g0259 a0002c0003t0003g0001 others(3): Show |
12 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-488G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495192 | |||||||
| chr12:27495478 | C | T | 57 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(54): Show |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.658-202C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495478 | |||||||
| chr12:27495522 | C | G | 37 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0003t0001g0027 others(34): Show |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.658-158C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495522 | |||||||
| chr12:27495560 | G | A | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.658-120G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 7/8 | chr12 | 27495560 | |||||||
| chr12:27495891 | A | T | 57 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(54): Show |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+36A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27495891 | |||||||
| chr12:27495998 | T | C | 5 | a0002c0002t0001g0047 a0002c0002t0003g0287 a0002c0002t0004g0245 others(2): Show |
5 | HG02145.hp1 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.833+143T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27495998 | |||||||
| chr12:27496061 | T | C | 1 | a0002c0003t0003g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.833+206T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496061 | |||||||
| chr12:27496148 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.833+293A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496148 | |||||||
| chr12:27496312 | C | G | 19 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(16): Show |
20 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833+457C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496312 | |||||||
| chr12:27496390 | A | C | 57 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(54): Show |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+535A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496390 | |||||||
| chr12:27496407 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.833+552A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496407 | |||||||
| chr12:27496621 | G | A | 35 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0003t0001g0027 others(32): Show |
49 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.833+766G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496621 | |||||||
| chr12:27496636 | C | T | 2 | a0002c0002t0002g0101 a0002c0002t0002g0102 |
2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.833+781C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496636 | |||||||
| chr12:27496798 | G | T | 4 | a0001c0001t0001g0229 a0001c0001t0002g0095 a0001c0001t0004g0234 others(1): Show |
4 | HG01243.hp2 HG01433.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.833+943G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496798 | |||||||
| chr12:27496867 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0002g0288 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.833+1012G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496867 | |||||||
| chr12:27496924 | G | A | 56 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0002t0001g0038 others(53): Show |
71 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.833+1069G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496924 | |||||||
| chr12:27496977 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.833+1122G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27496977 | |||||||
| chr12:27497174 | G | C | 1 | a0002c0003t0003g0141 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.833+1319G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497174 | |||||||
| chr12:27497278 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0230 |
2 | HG03688.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.833+1423T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497278 | |||||||
| chr12:27497360 | G | C | 57 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(54): Show |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.833+1505G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497360 | |||||||
| chr12:27497372 | A | C | 3 | a0001c0001t0001g0229 a0001c0001t0002g0095 a0001c0001t0004g0243 |
3 | HG01433.hp1 HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.833+1517A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497372 | |||||||
| chr12:27497498 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0156 a0001c0001t0001g0157 others(5): Show |
13 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(10): Show |
intron_variant | MODIFIER | c.833+1643C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497498 | |||||||
| chr12:27497499 | G | A | 1 | a0002c0002t0002g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.833+1644G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497499 | |||||||
| chr12:27497711 | T | C | 113 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0239 others(110): Show |
149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+1856T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497711 | |||||||
| chr12:27497732 | C | CA | 16 | a0001c0001t0001g0199 a0001c0001t0001g0227 a0001c0001t0001g0230 others(13): Show |
17 | HG00642.hp2 HG01106.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.833+1895dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | ||||||
| chr12:27497732 | C | CAAAA | 42 | a0001c0001t0001g0239 a0001c0001t0002g0037 a0001c0001t0002g0286 others(39): Show |
58 | HG00544.hp1 HG00733.hp2 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.833+1892_833+1895d others(6): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | ||||||
| chr12:27497732 | C | CAAAAA | 13 | a0002c0002t0001g0221 a0002c0002t0002g0004 a0002c0002t0002g0005 others(10): Show |
14 | HG00558.hp2 HG03239.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.833+1891_833+1895d others(7): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | ||||||
| chr12:27497732 | CA | C | 10 | a0001c0001t0001g0036 a0001c0001t0001g0171 a0001c0001t0001g0209 others(7): Show |
10 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.833+1895delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27497732 | ||||||
| chr12:27497790 | G | A | 1 | a0001c0005t0002g0008 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.833+1935G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497790 | |||||||
| chr12:27497819 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.833+1964A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27497819 | |||||||
| chr12:27498095 | T | C | 18 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.833+2240T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498095 | |||||||
| chr12:27498100 | A | C | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.833+2245A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498100 | |||||||
| chr12:27498146 | C | T | 1 | a0001c0001t0002g0285 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.833+2291C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498146 | |||||||
| chr12:27498158 | A | G | 1 | a0001c0005t0002g0061 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.833+2303A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498158 | |||||||
| chr12:27498218 | T | C | 113 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0239 others(110): Show |
149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+2363T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498218 | |||||||
| chr12:27498366 | A | T | 113 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0239 others(110): Show |
149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.833+2511A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498366 | |||||||
| chr12:27498520 | G | A | 18 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.833+2665G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498520 | |||||||
| chr12:27498603 | G | A | 2 | a0002c0003t0003g0150 a0002c0003t0003g0151 |
2 | NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.833+2748G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498603 | |||||||
| chr12:27498659 | T | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0001g0197 |
3 | HG00099.hp1 HG01175.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.833+2804T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498659 | |||||||
| chr12:27498982 | T | C | 4 | a0001c0001t0001g0239 a0002c0003t0001g0192 a0002c0003t0001g0222 others(1): Show |
4 | HG02300.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-2941T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27498982 | |||||||
| chr12:27499096 | C | G | 18 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-2827C>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499096 | |||||||
| chr12:27499194 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.834-2729G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499194 | |||||||
| chr12:27499717 | A | G | 18 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-2206A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499717 | |||||||
| chr12:27499855 | G | A | 3 | a0002c0003t0003g0022 a0002c0003t0003g0146 a0002c0003t0003g0152 |
4 | HG03239.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.834-2068G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499855 | |||||||
| chr12:27499860 | T | C | 1 | a0007c0010t0001g0232 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.834-2063T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499860 | |||||||
| chr12:27499870 | T | A | 1 | a0002c0002t0001g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.834-2053T>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27499870 | |||||||
| chr12:27500126 | A | C | 113 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0001c0001t0001g0239 others(110): Show |
149 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.834-1797A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500126 | |||||||
| chr12:27500148 | AT | A | 78 | a0001c0001t0001g0155 a0001c0001t0001g0239 a0001c0001t0001g0281 others(75): Show |
100 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(97): Show |
intron_variant | MODIFIER | c.834-1766delT | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27500148 | ||||||
| chr12:27500243 | T | C | 2 | a0002c0007t0001g0215 a0002c0007t0001g0276 |
2 | HG01884.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.834-1680T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500243 | |||||||
| chr12:27500286 | G | A | 2 | a0001c0001t0001g0007 a0002c0002t0002g0119 |
2 | NA19043.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.834-1637G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500286 | |||||||
| chr12:27500487 | CAAATTAT others(14): Show |
C | 57 | a0001c0001t0001g0239 a0001c0001t0001g0281 a0001c0001t0002g0037 others(54): Show |
78 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.834-1434_834-1414d others(23): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27500487 | ||||||
| chr12:27500635 | C | T | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.834-1288C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500635 | |||||||
| chr12:27500636 | G | A | 2 | a0001c0001t0001g0281 a0001c0001t0002g0288 |
2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.834-1287G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500636 | |||||||
| chr12:27500689 | C | T | 1 | a0002c0003t0003g0129 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.834-1234C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500689 | |||||||
| chr12:27500838 | C | T | 18 | a0002c0002t0001g0038 a0002c0002t0001g0047 a0002c0002t0003g0287 others(15): Show |
19 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.834-1085C>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500838 | |||||||
| chr12:27500885 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834-1038A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27500885 | |||||||
| chr12:27501078 | A | G | 1 | a0002c0002t0002g0010 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.834-845A>G | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501078 | |||||||
| chr12:27501114 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.834-809G>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501114 | |||||||
| chr12:27501379 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.834-544G>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501379 | |||||||
| chr12:27501382 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834-541G>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501382 | |||||||
| chr12:27501386 | A | T | 1 | a0001c0001t0002g0089 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.834-537A>T | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501386 | |||||||
| chr12:27501415 | C | CA | 30 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0239 others(27): Show |
36 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.834-486dupA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | ||||||
| chr12:27501415 | C | CAA | 11 | a0001c0005t0002g0065 a0002c0002t0001g0038 a0002c0002t0002g0004 others(8): Show |
11 | HG01070.hp1 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.834-487_834-486dup others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | ||||||
| chr12:27501415 | CA | C | 22 | a0001c0001t0001g0168 a0001c0001t0002g0016 a0001c0001t0002g0017 others(19): Show |
25 | HG00544.hp2 HG01255.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.834-486delA | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | ||||||
| chr12:27501415 | CAA | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0026 others(38): Show |
43 | HG00099.hp1 HG00323.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.834-487_834-486del others(2): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | ||||||
| chr12:27501415 | CAAA | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(73): Show |
88 | HG00140.hp1 HG00280.hp2 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.834-488_834-486del others(3): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr12 | 27501415 | ||||||
| chr12:27501426 | A | AC | 12 | a0002c0003t0001g0251 a0002c0003t0003g0001 a0002c0003t0003g0006 others(9): Show |
21 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.834-497_834-496ins others(1): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501426 | |||||||
| chr12:27501430 | A | AC | 25 | a0001c0001t0001g0054 a0001c0001t0001g0194 a0002c0003t0001g0027 others(22): Show |
28 | HG00642.hp2 HG01884.hp2 HG02004.hp1 others(25): Show |
intron_variant | MODIFIER | c.834-493_834-492ins others(1): Show |
SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501430 | |||||||
| chr12:27501430 | A | C | 18 | a0001c0001t0001g0167 a0001c0001t0001g0172 a0001c0001t0001g0229 others(15): Show |
27 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.834-493A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501430 | |||||||
| chr12:27501434 | A | C | 66 | a0001c0001t0001g0024 a0001c0001t0001g0029 a0001c0001t0001g0030 others(63): Show |
83 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.834-489A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501434 | |||||||
| chr12:27501438 | C | A | 74 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0183 others(71): Show |
96 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.834-485C>A | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501438 | |||||||
| chr12:27501596 | A | C | 60 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0183 others(57): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.834-327A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501596 | |||||||
| chr12:27501613 | A | C | 60 | a0001c0001t0001g0024 a0001c0001t0001g0181 a0001c0001t0001g0183 others(57): Show |
81 | HG00544.hp1 HG00558.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.834-310A>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501613 | |||||||
| chr12:27501909 | T | C | 1 | a0002c0003t0004g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.834-14T>C | SMCO2 | ENSG00000165935.10 | transcript | ENST00000535986.2 | protein_coding | 8/8 | chr12 | 27501909 |