Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51559 |
| ensemblid | ENSG00000111696.12 |
| hgncid | 30826 |
| symbol | NT5DC3 |
| name | 5'-nucleotidase domain containing 3 |
| refseq_nuc | NM_001031701.3 |
| refseq_prot | NP_001026871.1 |
| ensembl_nuc | ENST00000392876.8 |
| ensembl_prot | ENSP00000376615.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 103772310 |
| end | 103841234 |
| strand | - |
| ver | v1.2 |
| region | chr12:103772310-103841234 |
| region5000 | chr12:103767310-103846234 |
| regionname0 | NT5DC3_chr12_103772310_103841234 |
| regionname5000 | NT5DC3_chr12_103767310_103846234 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 383 | 94 | 80 | 147 | 18 | 42 | 120 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | MTMAA others(543): Show |
chr12 | 103767310 | 103846234 |
| a0002 | 0/0 | 548 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | MTMAA others(543): Show |
chr12 | 103767310 | 103846234 |
| a0003 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | MTMAA others(543): Show |
chr12 | 103767310 | 103846234 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1644 | 111 | 57 | 32 | 6 | 3 | 12 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0002 | 0/1 | 1644 | 105 | 20 | 22 | 44 | 7 | 11 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0003 | 0/0 | 1644 | 62 | 0 | 14 | 43 | 2 | 3 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0004 | 0/0 | 1644 | 47 | 5 | 2 | 33 | 0 | 7 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0005 | 0/0 | 1644 | 46 | 7 | 9 | 21 | 5 | 4 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0006 | 0/0 | 1644 | 10 | 4 | 1 | 0 | 1 | 4 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0008 | 0/0 | 1644 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0001c0009 | 0/0 | 1644 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0002c0007 | 0/0 | 1644 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 | ||
| a0003c0010 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | ATGAC others(1639): Show |
chr12 | 103767310 | 103846234 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7241 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0004 | 1/0 | 7244 | 21 | 13 | 3 | 0 | 1 | 3 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0005 | 0/0 | 7244 | 32 | 7 | 16 | 5 | 0 | 4 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0006 | 0/0 | 7240 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0007 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0009 | 0/0 | 7244 | 9 | 9 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0010 | 0/0 | 7244 | 8 | 7 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0014 | 0/0 | 7244 | 4 | 3 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0022 | 0/0 | 7239 | 2 | 0 | 1 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7234): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0026 | 0/0 | 7243 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0027 | 0/0 | 7243 | 3 | 2 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0028 | 0/0 | 7245 | 3 | 0 | 3 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0030 | 0/0 | 7241 | 2 | 0 | 1 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0033 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0034 | 0/0 | 7244 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0035 | 0/0 | 7245 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0036 | 0/0 | 7243 | 2 | 1 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0037 | 0/0 | 7245 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0038 | 0/0 | 7243 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0039 | 0/0 | 7245 | 2 | 1 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0068 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0070 | 0/0 | 7244 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0072 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0073 | 0/0 | 7243 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0074 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0075 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0079 | 0/0 | 7243 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0083 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0001t0084 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0001 | 0/0 | 7241 | 54 | 6 | 12 | 27 | 3 | 6 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0005 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0006 | 0/0 | 7240 | 12 | 0 | 2 | 6 | 1 | 3 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0013 | 0/0 | 7240 | 6 | 1 | 3 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0014 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0016 | 0/0 | 7240 | 3 | 0 | 3 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0021 | 0/0 | 7240 | 3 | 0 | 1 | 0 | 2 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0022 | 0/0 | 7239 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7234): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0023 | 0/0 | 7241 | 3 | 0 | 0 | 3 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0024 | 0/0 | 7241 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0025 | 0/0 | 7242 | 3 | 3 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7237): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0031 | 0/0 | 7242 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7237): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0038 | 0/0 | 7243 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0040 | 0/0 | 7244 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0043 | 0/1 | 7240 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0044 | 0/0 | 7241 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0045 | 0/0 | 7240 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0046 | 0/0 | 7241 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0047 | 0/0 | 7242 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7237): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0048 | 0/0 | 7242 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7237): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0049 | 0/0 | 7241 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0050 | 0/0 | 7243 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0051 | 0/0 | 7240 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0002t0076 | 0/0 | 7243 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0002 | 0/0 | 7251 | 36 | 0 | 10 | 21 | 2 | 3 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0008 | 0/0 | 7247 | 10 | 0 | 2 | 8 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7242): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0018 | 0/0 | 7250 | 4 | 0 | 1 | 3 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0019 | 0/0 | 7252 | 4 | 0 | 0 | 4 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7247): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0058 | 0/0 | 7250 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0059 | 0/0 | 7250 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0060 | 0/0 | 7250 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0061 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0062 | 0/0 | 7252 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7247): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0063 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0064 | 0/0 | 7248 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7243): Show |
chr12 | 103767310 | 103846234 |
| a0001c0003t0065 | 0/0 | 7253 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7248): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0002 | 0/0 | 7251 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0003 | 0/0 | 7250 | 32 | 5 | 1 | 21 | 0 | 5 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0017 | 0/0 | 7249 | 4 | 0 | 0 | 3 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7244): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0032 | 0/0 | 7251 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0052 | 0/0 | 7252 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7247): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0053 | 0/0 | 7249 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7244): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0054 | 0/0 | 7250 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0055 | 0/0 | 7250 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0056 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0057 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0066 | 0/0 | 7240 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0004t0067 | 0/0 | 7241 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7236): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0004 | 0/0 | 7244 | 12 | 5 | 5 | 0 | 1 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0007 | 0/0 | 7244 | 10 | 0 | 0 | 9 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0011 | 0/0 | 7244 | 7 | 1 | 2 | 0 | 2 | 2 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0015 | 0/0 | 7244 | 4 | 0 | 0 | 4 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0026 | 0/0 | 7243 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0029 | 0/0 | 7243 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0033 | 0/0 | 7244 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0041 | 0/0 | 7244 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0069 | 0/0 | 7243 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0071 | 0/0 | 7244 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0077 | 0/0 | 7243 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0078 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0080 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7240): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0081 | 0/0 | 7246 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7241): Show |
chr12 | 103767310 | 103846234 |
| a0001c0005t0082 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0001c0006t0012 | 0/0 | 7248 | 6 | 4 | 0 | 0 | 0 | 2 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7243): Show |
chr12 | 103767310 | 103846234 |
| a0001c0006t0020 | 0/0 | 7248 | 3 | 0 | 1 | 0 | 1 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7243): Show |
chr12 | 103767310 | 103846234 |
| a0001c0006t0042 | 0/0 | 7249 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7244): Show |
chr12 | 103767310 | 103846234 |
| a0001c0008t0016 | 0/0 | 7240 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7235): Show |
chr12 | 103767310 | 103846234 |
| a0001c0009t0003 | 0/0 | 7250 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7245): Show |
chr12 | 103767310 | 103846234 |
| a0002c0007t0007 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7239): Show |
chr12 | 103767310 | 103846234 |
| a0002c0007t0029 | 0/0 | 7243 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7238): Show |
chr12 | 103767310 | 103846234 |
| a0003c0010t0002 | 0/0 | 7251 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | AGAGC others(7246): Show |
chr12 | 103767310 | 103846234 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0002 | 1/0 | 3 | 1 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0005g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0009g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0014g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0014g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0022g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0022g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0026g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0026g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0027g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0027g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0027g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0028g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0028g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0030g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0030g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0033g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0034g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0034g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0035g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0035g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0036g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0036g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0037g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0037g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0038g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0039g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0039g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0068g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0070g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0072g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0073g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0074g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0075g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0079g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0083g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0001t0084g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0006g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0013g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0014g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0016g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0016g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0016g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0021g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0022g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0023g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0023g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0023g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0024g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0024g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0024g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0025g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0025g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0031g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0031g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0038g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0040g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0040g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0043g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0044g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0045g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0046g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0047g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0048g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0049g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0050g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0051g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0002t0076g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0018g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0018g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0018g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0018g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0019g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0019g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0019g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0019g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0058g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0059g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0060g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0061g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0062g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0063g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0064g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0003t0065g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0017g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0017g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0017g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0017g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0032g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0032g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0052g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0053g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0054g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0055g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0056g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0057g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0066g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0004t0067g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0011g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0015g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0015g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0015g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0015g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0026g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0029g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0029g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0033g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0041g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0069g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0071g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0077g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0078g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0080g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0081g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0005t0082g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0020g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0020g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0020g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0006t0042g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0008t0016g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0001c0009t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0002c0007t0007g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0002c0007t0029g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| a0003c0010t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0011 | g0011 | EUR | GBR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00099 | hp2 | a0001 | c0001 | t0026 | g0084 | EUR | GBR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0242 | EUR | GBR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0263 | EUR | GBR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0325 | EUR | FIN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00280 | hp2 | a0001 | c0005 | t0004 | g0041 | EUR | FIN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00323 | hp1 | a0001 | c0006 | t0020 | g0175 | EUR | FIN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00323 | hp2 | a0001 | c0005 | t0077 | g0314 | EUR | FIN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00408 | hp1 | a0001 | c0005 | t0015 | g0015 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00408 | hp2 | a0001 | c0002 | t0006 | g0145 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00438 | hp1 | a0001 | c0004 | t0003 | g0101 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00438 | hp2 | a0001 | c0003 | t0008 | g0126 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00544 | hp2 | a0001 | c0004 | t0003 | g0212 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0143 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00609 | hp2 | a0001 | c0004 | t0067 | g0028 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00621 | hp1 | a0001 | c0005 | t0007 | g0320 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | CHS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00642 | hp2 | a0001 | c0005 | t0004 | g0161 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00733 | hp1 | a0001 | c0005 | t0004 | g0309 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00733 | hp2 | a0001 | c0003 | t0002 | g0367 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00735 | hp1 | a0001 | c0005 | t0004 | g0042 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00735 | hp2 | a0001 | c0003 | t0008 | g0125 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0266 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00738 | hp2 | a0001 | c0005 | t0011 | g0315 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG00741 | hp2 | a0001 | c0005 | t0078 | g0316 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0368 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01074 | hp1 | a0001 | c0002 | t0013 | g0288 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01081 | hp1 | a0001 | c0002 | t0013 | g0324 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0075 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0272 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01106 | hp1 | a0001 | c0002 | t0006 | g0253 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0355 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01167 | hp1 | a0001 | c0001 | t0036 | g0348 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01167 | hp2 | a0001 | c0001 | t0028 | g0003 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01169 | hp1 | a0001 | c0001 | t0028 | g0003 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0364 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01175 | hp2 | a0001 | c0005 | t0004 | g0160 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01192 | hp1 | a0001 | c0002 | t0006 | g0357 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01192 | hp2 | a0001 | c0005 | t0011 | g0243 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01243 | hp2 | a0001 | c0005 | t0033 | g0317 | AMR | PUR | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01255 | hp1 | a0001 | c0001 | t0030 | g0255 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01256 | hp1 | a0001 | c0001 | t0022 | g0244 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01256 | hp2 | a0001 | c0002 | t0021 | g0001 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01258 | hp2 | a0001 | c0001 | t0006 | g0245 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0358 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01358 | hp2 | a0001 | c0006 | t0020 | g0259 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0363 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01361 | hp2 | a0001 | c0005 | t0004 | g0307 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0035 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01433 | hp2 | a0001 | c0001 | t0028 | g0327 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01496 | hp1 | a0001 | c0003 | t0008 | g0121 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01496 | hp2 | a0001 | c0002 | t0076 | g0186 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01515 | hp1 | a0001 | c0001 | t0030 | g0108 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0372 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01516 | hp1 | a0001 | c0002 | t0022 | g0328 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01516 | hp2 | a0001 | c0002 | t0021 | g0001 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01517 | hp1 | a0001 | c0002 | t0021 | g0001 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0371 | EUR | IBS | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0049 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01884 | hp2 | a0001 | c0001 | t0027 | g0086 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01891 | hp2 | a0001 | c0001 | t0027 | g0341 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0025 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01928 | hp2 | a0001 | c0003 | t0062 | g0361 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0360 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01943 | hp1 | a0001 | c0001 | t0027 | g0349 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01943 | hp2 | a0001 | c0001 | t0026 | g0233 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01952 | hp1 | a0001 | c0003 | t0002 | g0359 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01952 | hp2 | a0001 | c0002 | t0016 | g0146 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01975 | hp1 | a0001 | c0003 | t0018 | g0369 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01978 | hp2 | a0001 | c0002 | t0016 | g0144 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01981 | hp2 | a0001 | c0001 | t0039 | g0030 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0356 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01993 | hp2 | a0001 | c0002 | t0013 | g0034 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0352 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02015 | hp1 | a0001 | c0004 | t0003 | g0100 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02015 | hp2 | a0001 | c0003 | t0060 | g0133 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0260 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0098 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02056 | hp2 | a0001 | c0005 | t0007 | g0305 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02080 | hp1 | a0001 | c0002 | t0023 | g0104 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02080 | hp2 | a0001 | c0004 | t0003 | g0091 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0169 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0061 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0338 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02135 | hp1 | a0001 | c0004 | t0052 | g0343 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02135 | hp2 | a0001 | c0005 | t0007 | g0194 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02145 | hp1 | a0001 | c0001 | t0072 | g0224 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0112 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0370 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0087 | EAS | CDX | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0362 | EAS | CDX | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0336 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02257 | hp2 | a0001 | c0001 | t0035 | g0337 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02258 | hp1 | a0001 | c0002 | t0024 | g0329 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02273 | hp1 | a0001 | c0004 | t0003 | g0022 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0037 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02280 | hp1 | a0001 | c0001 | t0039 | g0344 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02280 | hp2 | a0001 | c0006 | t0012 | g0254 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02300 | hp2 | a0001 | c0002 | t0016 | g0040 | AMR | PEL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02523 | hp1 | a0001 | c0004 | t0003 | g0006 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02572 | hp2 | a0001 | c0004 | t0003 | g0219 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02602 | hp1 | a0001 | c0002 | t0047 | g0071 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02602 | hp2 | a0001 | c0001 | t0070 | g0237 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02615 | hp1 | a0001 | c0006 | t0012 | g0269 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0334 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02622 | hp1 | a0001 | c0004 | t0003 | g0217 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0223 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02630 | hp1 | a0001 | c0002 | t0024 | g0331 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02630 | hp2 | a0001 | c0005 | t0004 | g0296 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02647 | hp2 | a0001 | c0005 | t0004 | g0333 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0182 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02698 | hp1 | a0001 | c0001 | t0073 | g0111 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02698 | hp2 | a0001 | c0004 | t0003 | g0208 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02717 | hp1 | a0001 | c0001 | t0033 | g0229 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02717 | hp2 | a0001 | c0002 | t0025 | g0280 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02735 | hp2 | a0001 | c0001 | t0022 | g0046 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02738 | hp2 | a0001 | c0005 | t0011 | g0303 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0346 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02809 | hp2 | a0001 | c0002 | t0040 | g0231 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02818 | hp1 | a0001 | c0001 | t0037 | g0351 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02886 | hp2 | a0001 | c0005 | t0004 | g0241 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0185 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02895 | hp2 | a0001 | c0004 | t0003 | g0159 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02896 | hp1 | a0001 | c0001 | t0038 | g0180 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02896 | hp2 | a0001 | c0001 | t0075 | g0294 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02922 | hp1 | a0001 | c0005 | t0069 | g0295 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02922 | hp2 | a0001 | c0002 | t0049 | g0350 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02965 | hp1 | a0001 | c0002 | t0038 | g0270 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02965 | hp2 | a0001 | c0001 | t0036 | g0222 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02970 | hp1 | a0001 | c0006 | t0012 | g0268 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02970 | hp2 | a0001 | c0001 | t0074 | g0258 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0345 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0063 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03017 | hp2 | a0001 | c0006 | t0020 | g0155 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03041 | hp1 | a0001 | c0002 | t0013 | g0249 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0326 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03139 | hp2 | a0001 | c0001 | t0068 | g0267 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03195 | hp1 | a0001 | c0002 | t0050 | g0330 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0342 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03209 | hp2 | a0001 | c0001 | t0035 | g0181 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03225 | hp1 | a0001 | c0002 | t0025 | g0009 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03225 | hp2 | a0001 | c0002 | t0014 | g0163 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0365 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0232 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0218 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03491 | hp1 | a0001 | c0001 | t0079 | g0230 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03491 | hp2 | a0001 | c0006 | t0012 | g0168 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03492 | hp2 | a0001 | c0006 | t0012 | g0167 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03516 | hp1 | a0001 | c0005 | t0004 | g0354 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0239 | AFR | ESN | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0347 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03540 | hp2 | a0001 | c0005 | t0004 | g0353 | AFR | GWD | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03579 | hp1 | a0001 | c0002 | t0040 | g0187 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0205 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03654 | hp2 | a0001 | c0004 | t0003 | g0089 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03669 | hp1 | a0001 | c0004 | t0017 | g0209 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03669 | hp2 | a0001 | c0002 | t0045 | g0026 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03704 | hp1 | a0001 | c0002 | t0006 | g0170 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03704 | hp2 | a0001 | c0006 | t0042 | g0174 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03710 | hp1 | a0001 | c0005 | t0004 | g0286 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03710 | hp2 | a0001 | c0004 | t0003 | g0207 | SAS | PJL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03831 | hp1 | a0001 | c0004 | t0003 | g0158 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0153 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03834 | hp2 | a0001 | c0004 | t0057 | g0210 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03927 | hp1 | a0001 | c0005 | t0011 | g0318 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | BEB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04115 | hp2 | a0001 | c0004 | t0003 | g0192 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04199 | hp1 | a0001 | c0002 | t0006 | g0032 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04199 | hp2 | a0001 | c0002 | t0006 | g0066 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0107 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04204 | hp2 | a0001 | c0009 | t0003 | g0216 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0166 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG04228 | hp2 | a0001 | c0005 | t0007 | g0096 | SAS | STU | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0240 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18522 | hp2 | a0001 | c0001 | t0034 | g0274 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18747 | hp1 | a0001 | c0003 | t0018 | g0135 | EAS | CHB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18747 | hp2 | a0002 | c0007 | t0029 | g0308 | EAS | CHB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18939 | hp1 | a0001 | c0002 | t0044 | g0157 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18939 | hp2 | a0001 | c0005 | t0082 | g0102 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18941 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18942 | hp1 | a0001 | c0004 | t0003 | g0213 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18945 | hp1 | a0001 | c0003 | t0064 | g0131 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18946 | hp2 | a0001 | c0004 | t0003 | g0215 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18951 | hp1 | a0001 | c0005 | t0026 | g0281 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18951 | hp2 | a0001 | c0004 | t0003 | g0214 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18952 | hp1 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18952 | hp2 | a0001 | c0004 | t0017 | g0019 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18953 | hp1 | a0001 | c0005 | t0007 | g0225 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18953 | hp2 | a0001 | c0002 | t0013 | g0195 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18954 | hp1 | a0001 | c0004 | t0003 | g0293 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18954 | hp2 | a0001 | c0003 | t0008 | g0132 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18959 | hp1 | a0001 | c0003 | t0008 | g0138 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18960 | hp1 | a0001 | c0003 | t0002 | g0123 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18960 | hp2 | a0001 | c0003 | t0058 | g0179 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18962 | hp1 | a0001 | c0002 | t0023 | g0289 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18962 | hp2 | a0001 | c0005 | t0029 | g0092 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18963 | hp1 | a0001 | c0005 | t0007 | g0306 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18964 | hp1 | a0001 | c0005 | t0041 | g0012 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18965 | hp2 | a0001 | c0004 | t0003 | g0211 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0283 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18967 | hp1 | a0001 | c0005 | t0007 | g0321 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18969 | hp1 | a0001 | c0003 | t0018 | g0137 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18969 | hp2 | a0001 | c0004 | t0003 | g0006 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18973 | hp1 | a0001 | c0005 | t0007 | g0304 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18973 | hp2 | a0001 | c0004 | t0003 | g0079 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18974 | hp1 | a0001 | c0003 | t0065 | g0062 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18974 | hp2 | a0001 | c0004 | t0003 | g0152 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18975 | hp2 | a0001 | c0004 | t0003 | g0221 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18977 | hp1 | a0001 | c0002 | t0006 | g0173 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18977 | hp2 | a0001 | c0003 | t0019 | g0177 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18978 | hp1 | a0001 | c0005 | t0007 | g0193 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18983 | hp1 | a0001 | c0002 | t0006 | g0064 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18983 | hp2 | a0001 | c0004 | t0003 | g0020 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18986 | hp1 | a0001 | c0005 | t0015 | g0014 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18986 | hp2 | a0001 | c0004 | t0017 | g0076 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18987 | hp1 | a0001 | c0005 | t0080 | g0312 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18987 | hp2 | a0001 | c0002 | t0046 | g0059 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18988 | hp2 | a0001 | c0005 | t0015 | g0016 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18989 | hp2 | a0001 | c0003 | t0008 | g0128 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18992 | hp1 | a0001 | c0004 | t0055 | g0301 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18992 | hp2 | a0001 | c0002 | t0013 | g0069 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18993 | hp1 | a0001 | c0003 | t0018 | g0140 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0080 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18995 | hp1 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0284 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18998 | hp2 | a0001 | c0004 | t0003 | g0093 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19000 | hp1 | a0001 | c0002 | t0031 | g0339 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19000 | hp2 | a0003 | c0010 | t0002 | g0282 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19001 | hp1 | a0001 | c0003 | t0008 | g0130 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19002 | hp1 | a0001 | c0003 | t0008 | g0141 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19002 | hp2 | a0001 | c0004 | t0017 | g0150 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19003 | hp2 | a0001 | c0004 | t0003 | g0302 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19007 | hp2 | a0001 | c0002 | t0006 | g0010 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19009 | hp1 | a0001 | c0004 | t0003 | g0078 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19009 | hp2 | a0001 | c0002 | t0031 | g0199 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19010 | hp1 | a0001 | c0002 | t0023 | g0072 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19010 | hp2 | a0001 | c0003 | t0061 | g0178 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19011 | hp1 | a0001 | c0003 | t0002 | g0287 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19011 | hp2 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19012 | hp1 | a0001 | c0002 | t0006 | g0065 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19012 | hp2 | a0001 | c0004 | t0053 | g0206 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19030 | hp1 | a0001 | c0001 | t0037 | g0335 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19030 | hp2 | a0001 | c0002 | t0005 | g0188 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19043 | hp1 | a0001 | c0004 | t0003 | g0261 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19054 | hp2 | a0001 | c0003 | t0019 | g0118 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19056 | hp2 | a0001 | c0002 | t0051 | g0183 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19057 | hp1 | a0001 | c0005 | t0029 | g0310 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19057 | hp2 | a0001 | c0003 | t0002 | g0097 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19062 | hp1 | a0001 | c0005 | t0007 | g0311 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19064 | hp1 | a0001 | c0003 | t0063 | g0189 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19064 | hp2 | a0001 | c0004 | t0066 | g0027 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19066 | hp1 | a0001 | c0004 | t0056 | g0081 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19070 | hp1 | a0001 | c0004 | t0032 | g0220 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19070 | hp2 | a0002 | c0007 | t0007 | g0319 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19078 | hp1 | a0001 | c0003 | t0008 | g0139 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19078 | hp2 | a0001 | c0002 | t0048 | g0202 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19080 | hp1 | a0001 | c0004 | t0054 | g0292 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19082 | hp1 | a0001 | c0005 | t0081 | g0313 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19082 | hp2 | a0001 | c0004 | t0003 | g0090 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19084 | hp1 | a0001 | c0003 | t0019 | g0119 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19084 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19085 | hp2 | a0001 | c0003 | t0019 | g0120 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19086 | hp2 | a0001 | c0003 | t0059 | g0122 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19088 | hp1 | a0001 | c0004 | t0032 | g0077 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19091 | hp1 | a0001 | c0005 | t0041 | g0012 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19091 | hp2 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19240 | hp1 | a0001 | c0001 | t0014 | g0257 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | YRI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20129 | hp1 | a0001 | c0002 | t0025 | g0009 | AFR | ASW | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ASW | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20752 | hp1 | a0001 | c0005 | t0071 | g0083 | EUR | TSI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0291 | EUR | TSI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20805 | hp1 | a0001 | c0005 | t0011 | g0011 | EUR | TSI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20805 | hp2 | a0001 | c0002 | t0006 | g0252 | EUR | TSI | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0366 | SAS | GIH | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0106 | SAS | GIH | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0051 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0054 | AMR | CLM | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02109 | hp1 | a0001 | c0006 | t0012 | g0256 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0271 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG02559 | hp2 | a0001 | c0001 | t0083 | g0238 | AFR | ACB | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0005 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG03471 | hp2 | a0001 | c0002 | t0024 | g0332 | AFR | MSL | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG06807 | hp1 | a0001 | c0005 | t0011 | g0023 | AFR | USA | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| HG06807 | hp2 | a0001 | c0001 | t0084 | g0165 | AFR | USA | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18955 | hp1 | a0001 | c0003 | t0008 | g0127 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA18955 | hp2 | a0001 | c0005 | t0015 | g0013 | EAS | JPT | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20300 | hp1 | a0001 | c0008 | t0016 | g0017 | AFR | USA | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA20300 | hp2 | a0001 | c0001 | t0034 | g0162 | AFR | USA | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0323 | AFR | LWK | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0043 | g0114 | REF | REF | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0002 | REF | REF | NT5DC3_chr12_103767310_103846234 | NT5DC3 | chr12 | 103767310 | 103846234 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103780353 | A | C | 1 | a0002 | 2 | NA18747.hp2 NA19070.hp2 |
missense_variant | MODERATE | c.1341T>G | p.Asp447Glu | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/14 | 1419/7244 | 1341/1647 | 447/548 | chr12 | 103780353 | |||
| chr12:103798660 | G | A | 1 | a0003 | 1 | NA19000.hp2 | missense_variant | MODERATE | c.542C>T | p.Pro181Leu | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/14 | 620/7244 | 542/1647 | 181/548 | chr12 | 103798660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103777964 | C | T | 5 | a0001c0003 a0001c0004 a0001c0006 others(2): Show |
121 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
synonymous_variant | LOW | c.1512G>A | p.Leu504Leu | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1590/7244 | 1512/1647 | 504/548 | chr12 | 103777964 | |||
| chr12:103793168 | G | T | 4 | a0001c0002 a0001c0004 a0001c0008 others(1): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
synonymous_variant | LOW | c.1015C>A | p.Arg339Arg | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/14 | 1093/7244 | 1015/1647 | 339/548 | chr12 | 103793168 | |||
| chr12:103793217 | G | A | 2 | a0001c0003 a0003c0010 |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
synonymous_variant | LOW | c.966C>T | p.Phe322Phe | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/14 | 1044/7244 | 966/1647 | 322/548 | chr12 | 103793217 | |||
| chr12:103798623 | G | A | 1 | a0001c0009 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.579C>T | p.His193His | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/14 | 657/7244 | 579/1647 | 193/548 | chr12 | 103798623 | |||
| chr12:103815090 | C | T | 2 | a0001c0005 a0002c0007 |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
synonymous_variant | LOW | c.240G>A | p.Leu80Leu | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/14 | 318/7244 | 240/1647 | 80/548 | chr12 | 103815090 | |||
| chr12:103840986 | C | T | 1 | a0001c0008 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.171G>A | p.Leu57Leu | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/14 | 249/7244 | 171/1647 | 57/548 | chr12 | 103840986 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103772317 | C | T | 27 | a0001c0003t0002 a0001c0003t0008 a0001c0003t0018 others(24): Show |
119 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*5512G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5512 | chr12 | 103772317 | ||||||
| chr12:103772318 | A | C | 27 | a0001c0003t0002 a0001c0003t0008 a0001c0003t0018 others(24): Show |
119 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*5511T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5511 | chr12 | 103772318 | ||||||
| chr12:103772465 | C | T | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*5364G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5364 | chr12 | 103772465 | ||||||
| chr12:103772589 | G | A | 1 | a0001c0002t0049 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5240C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5240 | chr12 | 103772589 | ||||||
| chr12:103772692 | A | G | 1 | a0001c0002t0046 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5137T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5137 | chr12 | 103772692 | ||||||
| chr12:103772728 | C | T | 2 | a0001c0002t0016 a0001c0008t0016 |
4 | HG01952.hp2 HG01978.hp2 HG02300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5101G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5101 | chr12 | 103772728 | ||||||
| chr12:103772751 | C | A | 22 | a0001c0001t0005 a0001c0001t0009 a0001c0001t0010 others(19): Show |
79 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*5078G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5078 | chr12 | 103772751 | ||||||
| chr12:103772796 | G | C | 2 | a0001c0004t0053 a0001c0004t0055 |
2 | NA18992.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5033C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5033 | chr12 | 103772796 | ||||||
| chr12:103772810 | G | T | 1 | a0001c0002t0048 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5019C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 5019 | chr12 | 103772810 | ||||||
| chr12:103772851 | C | A | 1 | a0001c0004t0054 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4978G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4978 | chr12 | 103772851 | ||||||
| chr12:103772982 | T | G | 3 | a0001c0006t0012 a0001c0006t0020 a0001c0006t0042 |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4847A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4847 | chr12 | 103772982 | ||||||
| chr12:103773024 | A | T | 1 | a0001c0003t0059 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4805T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4805 | chr12 | 103773024 | ||||||
| chr12:103773111 | C | T | 1 | a0001c0002t0045 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4718G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4718 | chr12 | 103773111 | ||||||
| chr12:103773246 | T | C | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(18): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4583A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4583 | chr12 | 103773246 | ||||||
| chr12:103773266 | G | A | 1 | a0001c0006t0020 | 3 | HG00323.hp1 HG01358.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4563C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4563 | chr12 | 103773266 | ||||||
| chr12:103773407 | C | T | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(18): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*4422G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4422 | chr12 | 103773407 | ||||||
| chr12:103773555 | A | G | 1 | a0001c0003t0061 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4274T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4274 | chr12 | 103773555 | ||||||
| chr12:103773569 | A | G | 2 | a0001c0001t0010 a0001c0001t0027 |
11 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4260T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4260 | chr12 | 103773569 | ||||||
| chr12:103773604 | G | A | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*4225C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4225 | chr12 | 103773604 | ||||||
| chr12:103773608 | C | G | 1 | a0001c0001t0070 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4221G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4221 | chr12 | 103773608 | ||||||
| chr12:103773626 | A | G | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*4203T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4203 | chr12 | 103773626 | ||||||
| chr12:103773685 | C | A | 1 | a0001c0003t0060 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4144G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 4144 | chr12 | 103773685 | ||||||
| chr12:103773872 | G | C | 1 | a0001c0001t0037 | 2 | HG02818.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3957C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3957 | chr12 | 103773872 | ||||||
| chr12:103774080 | C | G | 4 | a0001c0002t0024 a0001c0002t0025 a0001c0002t0049 others(1): Show |
8 | HG02258.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3749G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3749 | chr12 | 103774080 | ||||||
| chr12:103774175 | G | A | 2 | a0001c0004t0053 a0001c0004t0055 |
2 | NA18992.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3654C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3654 | chr12 | 103774175 | ||||||
| chr12:103774190 | T | G | 1 | a0001c0001t0074 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3639A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3639 | chr12 | 103774190 | ||||||
| chr12:103774309 | A | G | 74 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(71): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*3520T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3520 | chr12 | 103774309 | ||||||
| chr12:103774387 | T | C | 1 | a0001c0005t0071 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3442A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3442 | chr12 | 103774387 | ||||||
| chr12:103774393 | C | T | 2 | a0001c0001t0014 a0001c0002t0014 |
5 | HG02257.hp1 HG02895.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3436G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3436 | chr12 | 103774393 | ||||||
| chr12:103774485 | C | A | 27 | a0001c0003t0002 a0001c0003t0008 a0001c0003t0018 others(24): Show |
119 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*3344G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3344 | chr12 | 103774485 | ||||||
| chr12:103774491 | G | A | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3338C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3338 | chr12 | 103774491 | ||||||
| chr12:103774548 | G | A | 1 | a0001c0003t0058 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3281C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3281 | chr12 | 103774548 | ||||||
| chr12:103774577 | G | A | 3 | a0001c0006t0012 a0001c0006t0020 a0001c0006t0042 |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3252C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3252 | chr12 | 103774577 | ||||||
| chr12:103774603 | G | A | 1 | a0001c0002t0021 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3226C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3226 | chr12 | 103774603 | ||||||
| chr12:103774653 | C | T | 1 | a0001c0002t0021 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3176G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3176 | chr12 | 103774653 | ||||||
| chr12:103774684 | C | CA | 11 | a0001c0001t0028 a0001c0001t0068 a0001c0001t0074 others(8): Show |
16 | HG01167.hp2 HG01169.hp1 HG01433.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3144dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3144 | chr12 | 103774684 | ||||||
| chr12:103774684 | CA | C | 24 | a0001c0001t0022 a0001c0001t0026 a0001c0001t0027 others(21): Show |
50 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3144delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3144 | chr12 | 103774684 | ||||||
| chr12:103774684 | CAAAA | C | 2 | a0001c0003t0008 a0001c0003t0064 |
11 | HG00438.hp2 HG00735.hp2 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3141_*3144delTTTT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3141 | chr12 | 103774684 | ||||||
| chr12:103774704 | A | G | 1 | a0001c0002t0023 | 3 | HG02080.hp1 NA18962.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3125T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3125 | chr12 | 103774704 | ||||||
| chr12:103774792 | T | C | 1 | a0001c0003t0063 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3037A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 3037 | chr12 | 103774792 | ||||||
| chr12:103774918 | G | A | 13 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0027 others(10): Show |
32 | HG01081.hp2 HG01496.hp2 HG01884.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2911C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2911 | chr12 | 103774918 | ||||||
| chr12:103774992 | C | T | 2 | a0001c0005t0041 a0001c0005t0081 |
3 | NA18964.hp1 NA19082.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2837G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2837 | chr12 | 103774992 | ||||||
| chr12:103775010 | C | CA | 40 | a0001c0001t0001 a0001c0001t0030 a0001c0001t0035 others(37): Show |
192 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*2818dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2818 | chr12 | 103775010 | ||||||
| chr12:103775010 | C | CAA | 8 | a0001c0002t0031 a0001c0002t0048 a0001c0002t0050 others(5): Show |
12 | HG02135.hp1 HG03195.hp1 NA18945.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2817_*2818dupTT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2818 | chr12 | 103775010 | ||||||
| chr12:103775010 | CA | C | 6 | a0001c0001t0073 a0001c0001t0079 a0001c0005t0069 others(3): Show |
13 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2818delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2818 | chr12 | 103775010 | ||||||
| chr12:103775098 | G | A | 3 | a0001c0006t0012 a0001c0006t0020 a0001c0006t0042 |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2731C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2731 | chr12 | 103775098 | ||||||
| chr12:103775130 | C | T | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(18): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*2699G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2699 | chr12 | 103775130 | ||||||
| chr12:103775204 | T | C | 74 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(71): Show |
306 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*2625A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2625 | chr12 | 103775204 | ||||||
| chr12:103775309 | A | AG | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2519_*2520insC | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2519 | chr12 | 103775309 | ||||||
| chr12:103775358 | T | C | 1 | a0001c0001t0075 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2471A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2471 | chr12 | 103775358 | ||||||
| chr12:103775578 | C | T | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2251G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2251 | chr12 | 103775578 | ||||||
| chr12:103775586 | A | G | 2 | a0001c0001t0030 a0001c0002t0021 |
5 | HG01255.hp1 HG01256.hp2 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2243T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2243 | chr12 | 103775586 | ||||||
| chr12:103775721 | G | GAAGAA | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*2107_*2108insTTCT others(1): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 2107 | chr12 | 103775721 | ||||||
| chr12:103776050 | T | C | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1779A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1779 | chr12 | 103776050 | ||||||
| chr12:103776174 | T | C | 2 | a0001c0002t0040 a0001c0002t0076 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1655A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1655 | chr12 | 103776174 | ||||||
| chr12:103776179 | G | A | 10 | a0001c0004t0003 a0001c0004t0017 a0001c0004t0032 others(7): Show |
45 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1650C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1650 | chr12 | 103776179 | ||||||
| chr12:103776196 | G | A | 3 | a0001c0005t0011 a0001c0005t0077 a0001c0005t0078 |
9 | HG00099.hp1 HG00323.hp2 HG00738.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1633C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1633 | chr12 | 103776196 | ||||||
| chr12:103776346 | G | A | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1483C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1483 | chr12 | 103776346 | ||||||
| chr12:103776370 | A | C | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(18): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1459T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1459 | chr12 | 103776370 | ||||||
| chr12:103776409 | G | T | 1 | a0001c0001t0035 | 2 | HG02257.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1420C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1420 | chr12 | 103776409 | ||||||
| chr12:103776469 | C | T | 1 | a0001c0001t0034 | 2 | NA18522.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1360G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1360 | chr12 | 103776469 | ||||||
| chr12:103776520 | A | G | 4 | a0001c0002t0024 a0001c0002t0025 a0001c0002t0049 others(1): Show |
8 | HG02258.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1309T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1309 | chr12 | 103776520 | ||||||
| chr12:103776573 | G | A | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1256C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1256 | chr12 | 103776573 | ||||||
| chr12:103776579 | G | C | 1 | a0001c0001t0028 | 3 | HG01167.hp2 HG01169.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1250C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1250 | chr12 | 103776579 | ||||||
| chr12:103776631 | C | T | 1 | a0001c0002t0044 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1198 | chr12 | 103776631 | ||||||
| chr12:103776673 | AC | A | 9 | a0001c0004t0003 a0001c0004t0017 a0001c0004t0032 others(6): Show |
44 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1155delG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1155 | chr12 | 103776673 | ||||||
| chr12:103776674 | C | A | 1 | a0001c0004t0052 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1155G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1155 | chr12 | 103776674 | ||||||
| chr12:103776674 | C | CA | 10 | a0001c0001t0005 a0001c0001t0028 a0001c0001t0039 others(7): Show |
39 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1154dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1154 | chr12 | 103776674 | ||||||
| chr12:103776674 | CA | C | 27 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(24): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1154delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1154 | chr12 | 103776674 | ||||||
| chr12:103776678 | A | C | 1 | a0001c0001t0068 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1151T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1151 | chr12 | 103776678 | ||||||
| chr12:103776679 | A | C | 2 | a0001c0001t0033 a0001c0005t0033 |
2 | HG01243.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1150T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1150 | chr12 | 103776679 | ||||||
| chr12:103776689 | C | A | 2 | a0001c0001t0079 a0001c0004t0057 |
2 | HG03491.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1140G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1140 | chr12 | 103776689 | ||||||
| chr12:103776696 | C | T | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1133G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 1133 | chr12 | 103776696 | ||||||
| chr12:103777094 | C | T | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(18): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*735G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 735 | chr12 | 103777094 | ||||||
| chr12:103777147 | C | T | 10 | a0001c0004t0003 a0001c0004t0017 a0001c0004t0032 others(7): Show |
45 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*682G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 682 | chr12 | 103777147 | ||||||
| chr12:103777154 | CCTCCTCC others(3): Show |
C | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(22): Show |
108 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*665_*674delCATGGA others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 665 | chr12 | 103777154 | ||||||
| chr12:103777213 | G | A | 10 | a0001c0001t0007 a0001c0005t0007 a0001c0005t0015 others(7): Show |
24 | HG00408.hp1 HG00621.hp1 HG02056.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*616C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 616 | chr12 | 103777213 | ||||||
| chr12:103777274 | T | C | 1 | a0001c0002t0051 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*555A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 555 | chr12 | 103777274 | ||||||
| chr12:103777445 | G | A | 1 | a0001c0001t0083 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 384 | chr12 | 103777445 | ||||||
| chr12:103777493 | C | G | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(49): Show |
227 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*336G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 336 | chr12 | 103777493 | ||||||
| chr12:103777521 | G | A | 1 | a0001c0001t0084 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*308C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 308 | chr12 | 103777521 | ||||||
| chr12:103777677 | C | T | 23 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0022 others(20): Show |
106 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*152G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 152 | chr12 | 103777677 | ||||||
| chr12:103777725 | C | T | 3 | a0001c0006t0012 a0001c0006t0020 a0001c0006t0042 |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*104G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 14/14 | 104 | chr12 | 103777725 | ||||||
| chr12:103841226 | C | G | 1 | a0001c0005t0015 | 4 | HG00408.hp1 NA18955.hp2 NA18986.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/14 | 70 | chr12 | 103841226 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:103778163 | CT | C | 4 | a0001c0003t0002g0097 a0001c0003t0002g0368 a0001c0003t0008g0138 others(1): Show |
4 | HG01070.hp2 NA18959.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-83delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778163 | |||||||
| chr12:103778168 | T | A | 1 | a0001c0002t0051g0183 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1395-87A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778168 | |||||||
| chr12:103778168 | T | TA | 96 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(93): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1395-88_1395-87ins others(1): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778168 | |||||||
| chr12:103778169 | T | A | 101 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1395-88A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778169 | |||||||
| chr12:103778170 | T | A | 162 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(159): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1395-89A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778170 | |||||||
| chr12:103778170 | TA | T | 7 | a0001c0001t0005g0272 a0001c0001t0026g0084 a0001c0004t0003g0302 others(4): Show |
7 | HG00099.hp2 HG01099.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395-90delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778170 | |||||||
| chr12:103778171 | A | T | 38 | a0001c0004t0003g0006 a0001c0004t0003g0020 a0001c0004t0003g0021 others(35): Show |
39 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(36): Show |
intron_variant | MODIFIER | c.1395-90T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778171 | |||||||
| chr12:103778172 | A | T | 1 | a0001c0004t0055g0301 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1395-91T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778172 | |||||||
| chr12:103778391 | C | T | 119 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(116): Show |
121 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1395-310G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778391 | |||||||
| chr12:103778410 | A | G | 10 | a0001c0006t0012g0167 a0001c0006t0012g0168 a0001c0006t0012g0254 others(7): Show |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1395-329T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778410 | |||||||
| chr12:103778447 | T | C | 222 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(219): Show |
228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1395-366A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778447 | |||||||
| chr12:103778472 | A | G | 1 | a0001c0002t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1395-391T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778472 | |||||||
| chr12:103778480 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1395-399C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778480 | |||||||
| chr12:103778518 | G | A | 2 | a0001c0003t0002g0097 a0001c0003t0002g0287 |
2 | NA19011.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1395-437C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778518 | |||||||
| chr12:103778556 | A | C | 1 | a0001c0003t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1395-475T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778556 | |||||||
| chr12:103778598 | C | T | 1 | a0001c0003t0002g0103 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1395-517G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778598 | |||||||
| chr12:103778741 | G | C | 94 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(91): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1395-660C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778741 | |||||||
| chr12:103778808 | AAAAAG | A | 14 | a0001c0002t0001g0068 a0001c0002t0001g0073 a0001c0002t0001g0117 others(11): Show |
14 | HG00544.hp1 HG00621.hp2 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.1395-732_1395-728d others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103778808 | |||||||
| chr12:103779001 | C | T | 44 | a0001c0004t0003g0006 a0001c0004t0003g0020 a0001c0004t0003g0021 others(41): Show |
45 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(42): Show |
intron_variant | MODIFIER | c.1395-920G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779001 | |||||||
| chr12:103779071 | A | G | 1 | a0001c0001t0005g0272 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1395-990T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779071 | |||||||
| chr12:103779252 | C | T | 1 | a0001c0001t0006g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1394+1048G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779252 | |||||||
| chr12:103779291 | C | T | 222 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(219): Show |
228 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1394+1009G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779291 | |||||||
| chr12:103779494 | A | C | 1 | a0001c0004t0003g0261 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1394+806T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779494 | |||||||
| chr12:103779532 | A | T | 97 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(94): Show |
100 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1394+768T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779532 | |||||||
| chr12:103779852 | T | C | 213 | a0001c0001t0001g0085 a0001c0001t0006g0245 a0001c0001t0006g0262 others(210): Show |
219 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1394+448A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779852 | |||||||
| chr12:103779853 | T | C | 45 | a0001c0001t0028g0327 a0001c0004t0003g0006 a0001c0004t0003g0020 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG01433.hp2 others(43): Show |
intron_variant | MODIFIER | c.1394+447A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779853 | |||||||
| chr12:103779860 | T | G | 1 | a0001c0006t0020g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1394+440A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779860 | |||||||
| chr12:103779868 | T | A | 2 | a0001c0002t0024g0331 a0001c0002t0024g0332 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1394+432A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779868 | |||||||
| chr12:103779899 | T | C | 1 | a0001c0001t0005g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1394+401A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779899 | |||||||
| chr12:103779926 | T | A | 45 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(42): Show |
46 | HG00323.hp1 HG01081.hp2 HG01358.hp2 others(43): Show |
intron_variant | MODIFIER | c.1394+374A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103779926 | |||||||
| chr12:103780102 | G | A | 111 | a0001c0002t0001g0297 a0001c0002t0001g0298 a0001c0002t0001g0299 others(108): Show |
113 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1394+198C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103780102 | |||||||
| chr12:103780219 | C | G | 1 | a0001c0005t0007g0305 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1394+81G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103780219 | |||||||
| chr12:103780271 | C | T | 2 | a0001c0005t0004g0353 a0001c0005t0004g0354 |
2 | HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1394+29G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103780271 | |||||||
| chr12:103780272 | G | A | 1 | a0001c0002t0047g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1394+28C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 13/13 | chr12 | 103780272 | |||||||
| chr12:103780414 | C | T | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1330-50G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103780414 | |||||||
| chr12:103780971 | T | TA | 65 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330-608dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103780971 | |||||||
| chr12:103780984 | AT | A | 209 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(206): Show |
215 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1330-621delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103780984 | |||||||
| chr12:103781133 | G | A | 1 | a0001c0002t0023g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1330-769C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781133 | |||||||
| chr12:103781161 | G | A | 23 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(20): Show |
25 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1330-797C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781161 | |||||||
| chr12:103781192 | G | C | 6 | a0001c0003t0002g0037 a0001c0003t0002g0051 a0001c0003t0002g0061 others(3): Show |
6 | HG01123.hp1 HG02132.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-828C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781192 | |||||||
| chr12:103781262 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1330-898C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781262 | |||||||
| chr12:103781266 | A | G | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-902T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781266 | |||||||
| chr12:103781360 | A | T | 101 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(98): Show |
105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.1330-996T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781360 | |||||||
| chr12:103781362 | A | G | 3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1330-998T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781362 | |||||||
| chr12:103781414 | G | T | 1 | a0001c0001t0009g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1330-1050C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781414 | |||||||
| chr12:103781431 | C | T | 10 | a0001c0006t0012g0167 a0001c0006t0012g0168 a0001c0006t0012g0254 others(7): Show |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1330-1067G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781431 | |||||||
| chr12:103781499 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1330-1135C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781499 | |||||||
| chr12:103781631 | T | C | 210 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1330-1267A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781631 | |||||||
| chr12:103781640 | AC | A | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1330-1277delG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781640 | |||||||
| chr12:103781797 | A | G | 210 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1330-1433T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781797 | |||||||
| chr12:103781851 | C | G | 3 | a0001c0001t0004g0031 a0001c0001t0004g0263 a0001c0001t0079g0230 |
3 | HG00140.hp2 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1330-1487G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781851 | |||||||
| chr12:103781992 | G | A | 5 | a0001c0002t0001g0242 a0001c0002t0001g0247 a0001c0002t0001g0248 others(2): Show |
5 | HG00140.hp1 HG01109.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1330-1628C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103781992 | |||||||
| chr12:103782028 | G | A | 6 | a0001c0003t0002g0037 a0001c0003t0002g0051 a0001c0003t0002g0061 others(3): Show |
6 | HG01123.hp1 HG02132.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1664C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782028 | |||||||
| chr12:103782072 | G | T | 2 | a0001c0001t0037g0335 a0001c0001t0037g0351 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1330-1708C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782072 | |||||||
| chr12:103782378 | AG | A | 94 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(91): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1330-2015delC | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782378 | |||||||
| chr12:103782379 | G | A | 119 | a0001c0001t0035g0181 a0001c0001t0035g0337 a0001c0002t0024g0329 others(116): Show |
122 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1330-2015C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782379 | |||||||
| chr12:103782434 | C | A | 107 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(104): Show |
109 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1330-2070G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782434 | |||||||
| chr12:103782457 | C | T | 6 | a0001c0003t0002g0169 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-2093G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782457 | |||||||
| chr12:103782468 | C | T | 94 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(91): Show |
97 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1330-2104G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782468 | |||||||
| chr12:103782514 | T | C | 110 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0037 others(107): Show |
112 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1330-2150A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782514 | |||||||
| chr12:103782517 | G | A | 107 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(104): Show |
109 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1330-2153C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782517 | |||||||
| chr12:103782616 | T | C | 2 | a0001c0003t0002g0123 a0001c0003t0002g0134 |
2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1330-2252A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782616 | |||||||
| chr12:103782639 | T | C | 1 | a0001c0002t0006g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1330-2275A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782639 | |||||||
| chr12:103782641 | C | G | 1 | a0001c0002t0006g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1330-2277G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782641 | |||||||
| chr12:103782663 | G | C | 1 | a0001c0005t0004g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1330-2299C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782663 | |||||||
| chr12:103782671 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1330-2307C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782671 | |||||||
| chr12:103782714 | C | G | 10 | a0001c0006t0012g0167 a0001c0006t0012g0168 a0001c0006t0012g0254 others(7): Show |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1330-2350G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782714 | |||||||
| chr12:103782781 | G | A | 2 | a0001c0003t0008g0138 a0001c0003t0008g0141 |
2 | NA18959.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1330-2417C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782781 | |||||||
| chr12:103782832 | C | T | 12 | a0001c0001t0035g0181 a0001c0001t0035g0337 a0001c0002t0024g0329 others(9): Show |
13 | HG01496.hp2 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1330-2468G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782832 | |||||||
| chr12:103782893 | G | C | 2 | a0001c0001t0037g0335 a0001c0001t0037g0351 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1329+2442C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103782893 | |||||||
| chr12:103783228 | T | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1329+2107A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783228 | |||||||
| chr12:103783245 | G | A | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2090C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783245 | |||||||
| chr12:103783247 | T | A | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2088A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783247 | |||||||
| chr12:103783248 | A | C | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2087T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783248 | |||||||
| chr12:103783251 | C | G | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2084G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783251 | |||||||
| chr12:103783253 | C | T | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2082G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783253 | |||||||
| chr12:103783255 | T | G | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2080A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783255 | |||||||
| chr12:103783257 | T | G | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2078A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783257 | |||||||
| chr12:103783258 | A | T | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2077T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783258 | |||||||
| chr12:103783259 | T | G | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2076A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783259 | |||||||
| chr12:103783260 | A | T | 1 | a0001c0001t0005g0056 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1329+2075T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783260 | |||||||
| chr12:103783303 | G | T | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1329+2032C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783303 | |||||||
| chr12:103783306 | C | A | 11 | a0001c0001t0005g0054 a0001c0001t0005g0109 a0001c0001t0005g0110 others(8): Show |
11 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1329+2029G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783306 | |||||||
| chr12:103783355 | C | A | 1 | a0001c0002t0001g0203 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1329+1980G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783355 | |||||||
| chr12:103783560 | G | A | 56 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(53): Show |
57 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.1329+1775C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783560 | |||||||
| chr12:103783567 | G | A | 1 | a0001c0006t0012g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1329+1768C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783567 | |||||||
| chr12:103783632 | T | A | 10 | a0001c0006t0012g0167 a0001c0006t0012g0168 a0001c0006t0012g0254 others(7): Show |
10 | HG00323.hp1 HG01358.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1329+1703A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783632 | |||||||
| chr12:103783792 | C | A | 1 | a0001c0004t0003g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1329+1543G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783792 | |||||||
| chr12:103783792 | C | CA | 102 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(99): Show |
106 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1329+1542dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783792 | |||||||
| chr12:103783792 | C | CAA | 90 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(87): Show |
91 | HG00544.hp2 HG00733.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.1329+1541_1329+154 others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783792 | |||||||
| chr12:103783792 | C | CAAA | 14 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(11): Show |
15 | HG00438.hp1 HG01081.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1329+1540_1329+154 others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783792 | |||||||
| chr12:103783803 | A | AAT | 39 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(36): Show |
40 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1329+1531_1329+153 others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783803 | |||||||
| chr12:103783890 | T | C | 245 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(242): Show |
252 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.1329+1445A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783890 | |||||||
| chr12:103783968 | C | T | 3 | a0001c0002t0001g0247 a0001c0002t0001g0250 a0001c0002t0013g0249 |
3 | HG01109.hp1 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1329+1367G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783968 | |||||||
| chr12:103783979 | G | C | 41 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(38): Show |
43 | HG01081.hp2 HG01496.hp2 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.1329+1356C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783979 | |||||||
| chr12:103783979 | G | T | 3 | a0001c0002t0024g0331 a0001c0002t0024g0332 a0001c0002t0049g0350 |
3 | HG02630.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1329+1356C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783979 | |||||||
| chr12:103783995 | C | T | 107 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(104): Show |
109 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1329+1340G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103783995 | |||||||
| chr12:103784122 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1329+1213C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784122 | |||||||
| chr12:103784374 | T | C | 2 | a0001c0001t0037g0335 a0001c0001t0037g0351 |
2 | HG02818.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1329+961A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784374 | |||||||
| chr12:103784451 | T | C | 246 | a0001c0001t0007g0142 a0001c0001t0009g0049 a0001c0001t0009g0239 others(243): Show |
253 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.1329+884A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784451 | |||||||
| chr12:103784602 | C | T | 2 | a0001c0001t0068g0267 a0001c0001t0074g0258 |
2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1329+733G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784602 | |||||||
| chr12:103784672 | G | A | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1329+663C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784672 | |||||||
| chr12:103784871 | G | T | 1 | a0001c0002t0006g0145 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1329+464C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784871 | |||||||
| chr12:103784953 | G | C | 301 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(298): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1329+382C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784953 | |||||||
| chr12:103784970 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1329+365G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103784970 | |||||||
| chr12:103785032 | G | T | 2 | a0001c0001t0028g0003 a0001c0001t0028g0327 |
3 | HG01167.hp2 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1329+303C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 12/13 | chr12 | 103785032 | |||||||
| chr12:103785493 | G | A | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1189-18C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785493 | |||||||
| chr12:103785696 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1189-221G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785696 | |||||||
| chr12:103785751 | T | TA | 39 | a0001c0001t0004g0031 a0001c0001t0004g0190 a0001c0001t0004g0223 others(36): Show |
39 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.1189-277dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | T | TAA | 11 | a0001c0001t0004g0184 a0001c0001t0004g0277 a0001c0001t0004g0278 others(8): Show |
11 | HG00609.hp1 HG01167.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.1189-278_1189-277d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | TA | T | 34 | a0001c0001t0009g0271 a0001c0001t0009g0345 a0001c0001t0009g0346 others(31): Show |
35 | HG00733.hp2 HG01070.hp2 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189-277delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | TAAA | T | 8 | a0001c0002t0024g0332 a0001c0004t0003g0079 a0001c0004t0003g0080 others(5): Show |
8 | HG00438.hp1 HG02080.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1189-279_1189-277d others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | TAAAA | T | 44 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(41): Show |
46 | HG00544.hp2 HG01891.hp1 HG02015.hp1 others(43): Show |
intron_variant | MODIFIER | c.1189-280_1189-277d others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | TAAAAAAA others(5): Show |
T | 43 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(40): Show |
45 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1189-288_1189-277d others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785751 | TAAAAAAA others(6): Show |
T | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1189-289_1189-277d others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785751 | |||||||
| chr12:103785845 | C | G | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1189-370G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785845 | |||||||
| chr12:103785850 | CTG | C | 4 | a0001c0001t0030g0108 a0001c0001t0030g0255 a0001c0002t0001g0099 others(1): Show |
6 | HG01255.hp1 HG01256.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1189-377_1189-376d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785850 | |||||||
| chr12:103785972 | C | A | 45 | a0001c0002t0005g0188 a0001c0004t0003g0006 a0001c0004t0003g0020 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(43): Show |
intron_variant | MODIFIER | c.1189-497G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103785972 | |||||||
| chr12:103786510 | AG | A | 6 | a0001c0006t0012g0167 a0001c0006t0012g0168 a0001c0006t0020g0155 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.1188+930delC | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786510 | |||||||
| chr12:103786529 | C | CAG | 320 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0190 others(317): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1188+910_1188+911d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786529 | |||||||
| chr12:103786552 | G | A | 1 | a0001c0002t0001g0338 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1188+889C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786552 | |||||||
| chr12:103786575 | T | C | 1 | a0001c0002t0046g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1188+866A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786575 | |||||||
| chr12:103786679 | T | C | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1188+762A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786679 | |||||||
| chr12:103786681 | A | AT | 35 | a0001c0001t0004g0275 a0001c0001t0004g0278 a0001c0001t0009g0049 others(32): Show |
36 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.1188+759dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTT | 108 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(105): Show |
112 | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1188+755_1188+759d others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTTT | 35 | a0001c0002t0001g0038 a0001c0002t0001g0053 a0001c0002t0001g0148 others(32): Show |
36 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1188+754_1188+759d others(8): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTTTT others(1): Show |
7 | a0001c0003t0002g0368 a0001c0003t0002g0372 a0001c0003t0008g0130 others(4): Show |
7 | HG01070.hp2 HG01515.hp2 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.1188+752_1188+759d others(10): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTTTT others(2): Show |
40 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0061 others(37): Show |
41 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1188+751_1188+759d others(11): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTTTT others(3): Show |
19 | a0001c0002t0040g0187 a0001c0002t0076g0186 a0001c0003t0002g0051 others(16): Show |
19 | HG00733.hp2 HG00735.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1188+750_1188+759d others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786681 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0040g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1188+749_1188+759d others(13): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786681 | |||||||
| chr12:103786722 | G | A | 1 | a0001c0002t0001g0033 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1188+719C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786722 | |||||||
| chr12:103786973 | A | G | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1188+468T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103786973 | |||||||
| chr12:103787074 | G | A | 2 | a0001c0001t0005g0166 a0001c0001t0005g0323 |
2 | HG04228.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1188+367C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787074 | |||||||
| chr12:103787094 | G | A | 43 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(40): Show |
45 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1188+347C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787094 | |||||||
| chr12:103787194 | A | ACTG | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1188+246_1188+247i others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787194 | |||||||
| chr12:103787256 | G | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1188+185C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787256 | |||||||
| chr12:103787258 | T | TA | 43 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(40): Show |
45 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1188+182dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787258 | |||||||
| chr12:103787258 | TA | T | 109 | a0001c0002t0001g0364 a0001c0002t0005g0188 a0001c0003t0002g0007 others(106): Show |
111 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1188+182delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 11/13 | chr12 | 103787258 | |||||||
| chr12:103787611 | ATTG | A | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1102-87_1102-85del others(3): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787611 | |||||||
| chr12:103787642 | A | T | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1102-115T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787642 | |||||||
| chr12:103787834 | A | G | 1 | a0001c0002t0021g0001 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1102-307T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787834 | |||||||
| chr12:103787838 | C | T | 62 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1102-311G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787838 | |||||||
| chr12:103787853 | C | T | 320 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0190 others(317): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1102-326G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787853 | |||||||
| chr12:103787889 | AC | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1102-363delG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787889 | |||||||
| chr12:103787893 | T | G | 1 | a0001c0005t0007g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1102-366A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787893 | |||||||
| chr12:103787999 | C | T | 9 | a0001c0001t0005g0029 a0001c0001t0005g0050 a0001c0001t0005g0052 others(6): Show |
9 | HG01975.hp2 HG01981.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102-472G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103787999 | |||||||
| chr12:103788135 | C | A | 12 | a0001c0001t0009g0271 a0001c0001t0010g0005 a0001c0001t0010g0018 others(9): Show |
13 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1102-608G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103788135 | |||||||
| chr12:103788346 | T | C | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1101+492A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103788346 | |||||||
| chr12:103788381 | G | A | 1 | a0001c0002t0006g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1101+457C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103788381 | |||||||
| chr12:103788511 | A | G | 1 | a0001c0002t0001g0352 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1101+327T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103788511 | |||||||
| chr12:103788680 | T | C | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1101+158A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 10/13 | chr12 | 103788680 | |||||||
| chr12:103789058 | T | C | 328 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(325): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.1020-139A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789058 | |||||||
| chr12:103789079 | G | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-160C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789079 | |||||||
| chr12:103789190 | A | G | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-271T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789190 | |||||||
| chr12:103789200 | A | G | 301 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(298): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1020-281T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789200 | |||||||
| chr12:103789261 | T | C | 2 | a0001c0004t0003g0100 a0001c0004t0003g0101 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1020-342A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789261 | |||||||
| chr12:103789423 | TCAAAAA | T | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-510_1020-505d others(8): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789423 | |||||||
| chr12:103789580 | C | T | 214 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(211): Show |
220 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1020-661G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789580 | |||||||
| chr12:103789629 | G | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1020-710C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789629 | |||||||
| chr12:103789653 | G | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-734C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789653 | |||||||
| chr12:103789674 | C | T | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-755G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789674 | |||||||
| chr12:103789678 | T | TA | 10 | a0001c0001t0004g0190 a0001c0001t0004g0223 a0001c0001t0004g0265 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1020-760dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789678 | |||||||
| chr12:103789862 | T | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-943A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789862 | |||||||
| chr12:103789864 | T | C | 1 | a0001c0004t0003g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1020-945A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789864 | |||||||
| chr12:103789880 | A | G | 301 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(298): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1020-961T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789880 | |||||||
| chr12:103789897 | C | T | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1020-978G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789897 | |||||||
| chr12:103789940 | T | C | 58 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(55): Show |
59 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.1020-1021A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103789940 | |||||||
| chr12:103790029 | T | G | 11 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(8): Show |
12 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1020-1110A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790029 | |||||||
| chr12:103790070 | C | T | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-1151G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790070 | |||||||
| chr12:103790107 | A | G | 301 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(298): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1020-1188T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790107 | |||||||
| chr12:103790174 | G | A | 55 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(52): Show |
56 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1020-1255C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790174 | |||||||
| chr12:103790190 | G | A | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-1271C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790190 | |||||||
| chr12:103790194 | T | G | 56 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.1020-1275A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790194 | |||||||
| chr12:103790291 | T | A | 3 | a0001c0001t0005g0113 a0001c0001t0014g0153 a0001c0001t0039g0344 |
3 | HG02280.hp1 HG03834.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1020-1372A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790291 | |||||||
| chr12:103790539 | G | C | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1020-1620C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790539 | |||||||
| chr12:103790539 | G | T | 1 | a0001c0002t0006g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1020-1620C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790539 | |||||||
| chr12:103790585 | T | C | 45 | a0001c0002t0005g0188 a0001c0004t0003g0006 a0001c0004t0003g0020 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(43): Show |
intron_variant | MODIFIER | c.1020-1666A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790585 | |||||||
| chr12:103790680 | C | T | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1020-1761G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790680 | |||||||
| chr12:103790694 | C | CT | 57 | a0001c0001t0001g0085 a0001c0001t0004g0190 a0001c0001t0004g0265 others(54): Show |
59 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1020-1776dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790694 | |||||||
| chr12:103790694 | C | CTT | 7 | a0001c0001t0004g0277 a0001c0001t0004g0278 a0001c0001t0005g0024 others(4): Show |
7 | HG01433.hp2 HG01978.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1020-1777_1020-177 others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790694 | |||||||
| chr12:103790694 | CT | C | 12 | a0001c0001t0014g0153 a0001c0001t0014g0185 a0001c0001t0014g0336 others(9): Show |
13 | HG00621.hp2 HG00642.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1020-1776delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790694 | |||||||
| chr12:103790694 | CTT | C | 86 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(83): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1020-1777_1020-177 others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790694 | |||||||
| chr12:103790694 | CTTTTTTT | C | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1020-1782_1020-177 others(11): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790694 | |||||||
| chr12:103790770 | G | GGCTCACT others(4): Show |
212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-1852_1020-185 others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790770 | |||||||
| chr12:103790775 | T | C | 7 | a0001c0001t0009g0239 a0001c0001t0009g0240 a0001c0001t0009g0326 others(4): Show |
7 | HG02615.hp2 HG02896.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-1856A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790775 | |||||||
| chr12:103790866 | T | C | 148 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1020-1947A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790866 | |||||||
| chr12:103790891 | A | G | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1020-1972T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790891 | |||||||
| chr12:103790932 | G | A | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1020-2013C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790932 | |||||||
| chr12:103790964 | T | C | 1 | a0001c0004t0003g0214 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1020-2045A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103790964 | |||||||
| chr12:103791021 | C | T | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1020-2102G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791021 | |||||||
| chr12:103791048 | T | C | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1019+2116A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791048 | |||||||
| chr12:103791106 | A | G | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1019+2058T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791106 | |||||||
| chr12:103791181 | T | C | 211 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.1019+1983A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791181 | |||||||
| chr12:103791181 | T | G | 1 | a0001c0003t0008g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1019+1983A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791181 | |||||||
| chr12:103791190 | G | C | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1019+1974C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791190 | |||||||
| chr12:103791191 | G | A | 56 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.1019+1973C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791191 | |||||||
| chr12:103791277 | G | A | 1 | a0001c0006t0020g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1019+1887C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791277 | |||||||
| chr12:103791354 | A | G | 213 | a0001c0001t0009g0049 a0001c0001t0022g0046 a0001c0001t0030g0108 others(210): Show |
219 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1019+1810T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791354 | |||||||
| chr12:103791386 | C | A | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1019+1778G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791386 | |||||||
| chr12:103791471 | G | A | 56 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.1019+1693C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791471 | |||||||
| chr12:103791479 | T | G | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1019+1685A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791479 | |||||||
| chr12:103791519 | C | T | 212 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(209): Show |
218 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.1019+1645G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791519 | |||||||
| chr12:103791653 | G | A | 92 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1019+1511C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791653 | |||||||
| chr12:103791718 | G | A | 149 | a0001c0001t0022g0046 a0001c0001t0030g0108 a0001c0001t0030g0255 others(146): Show |
154 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1019+1446C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791718 | |||||||
| chr12:103791883 | A | G | 64 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1019+1281T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791883 | |||||||
| chr12:103791915 | C | T | 148 | a0001c0001t0030g0108 a0001c0001t0030g0255 a0001c0002t0001g0033 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1019+1249G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103791915 | |||||||
| chr12:103792101 | G | A | 45 | a0001c0002t0005g0188 a0001c0004t0003g0006 a0001c0004t0003g0020 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(43): Show |
intron_variant | MODIFIER | c.1019+1063C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792101 | |||||||
| chr12:103792101 | G | C | 44 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(41): Show |
46 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1019+1063C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792101 | |||||||
| chr12:103792107 | C | T | 1 | a0001c0005t0007g0305 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1019+1057G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792107 | |||||||
| chr12:103792304 | G | A | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1019+860C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792304 | |||||||
| chr12:103792370 | C | T | 28 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(25): Show |
29 | HG01081.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1019+794G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792370 | |||||||
| chr12:103792415 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1019+749A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792415 | |||||||
| chr12:103792518 | G | T | 2 | a0001c0005t0004g0160 a0001c0005t0004g0161 |
2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1019+646C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792518 | |||||||
| chr12:103792623 | T | C | 1 | a0001c0006t0020g0259 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1019+541A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792623 | |||||||
| chr12:103792665 | G | A | 52 | a0001c0001t0009g0049 a0001c0001t0009g0239 a0001c0001t0009g0240 others(49): Show |
53 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1019+499C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792665 | |||||||
| chr12:103792877 | C | T | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1019+287G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792877 | |||||||
| chr12:103792884 | A | G | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+280T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792884 | |||||||
| chr12:103792890 | T | C | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1019+274A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792890 | |||||||
| chr12:103792996 | C | T | 6 | a0001c0001t0009g0345 a0001c0001t0009g0346 a0001c0001t0009g0347 others(3): Show |
6 | HG02809.hp1 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1019+168G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103792996 | |||||||
| chr12:103793017 | A | G | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1019+147T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 9/13 | chr12 | 103793017 | |||||||
| chr12:103793314 | G | A | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.918-49C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 8/13 | chr12 | 103793314 | |||||||
| chr12:103793641 | G | T | 23 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(20): Show |
25 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.815-129C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 7/13 | chr12 | 103793641 | |||||||
| chr12:103793662 | C | T | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.815-150G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 7/13 | chr12 | 103793662 | |||||||
| chr12:103793929 | G | A | 41 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(38): Show |
42 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.814+8C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 7/13 | chr12 | 103793929 | |||||||
| chr12:103794148 | C | CT | 87 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.754-152dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794148 | |||||||
| chr12:103794148 | C | CTT | 116 | a0001c0002t0001g0154 a0001c0002t0005g0188 a0001c0002t0006g0173 others(113): Show |
119 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.754-153_754-152dup others(2): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794148 | |||||||
| chr12:103794151 | C | T | 209 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(206): Show |
215 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.754-154G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794151 | |||||||
| chr12:103794154 | T | C | 2 | a0001c0001t0005g0166 a0001c0001t0005g0323 |
2 | HG04228.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.754-157A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794154 | |||||||
| chr12:103794183 | T | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.754-186A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794183 | |||||||
| chr12:103794215 | T | C | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-218A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794215 | |||||||
| chr12:103794226 | T | TGCAGCCT others(31): Show |
211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-267_754-230dup others(38): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794226 | |||||||
| chr12:103794308 | T | C | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-311A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794308 | |||||||
| chr12:103794524 | C | T | 1 | a0003c0010t0002g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.754-527G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794524 | |||||||
| chr12:103794607 | C | G | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-610G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794607 | |||||||
| chr12:103794610 | G | C | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-613C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794610 | |||||||
| chr12:103794629 | C | T | 1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.754-632G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794629 | |||||||
| chr12:103794698 | G | A | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.754-701C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794698 | |||||||
| chr12:103794745 | A | G | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.754-748T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794745 | |||||||
| chr12:103794835 | A | C | 1 | a0001c0003t0018g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.754-838T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794835 | |||||||
| chr12:103794992 | A | G | 65 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0037 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.754-995T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103794992 | |||||||
| chr12:103795054 | G | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.754-1057C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795054 | |||||||
| chr12:103795237 | G | A | 11 | a0001c0002t0001g0094 a0001c0002t0024g0329 a0001c0002t0024g0331 others(8): Show |
12 | HG01496.hp2 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.754-1240C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795237 | |||||||
| chr12:103795278 | A | G | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.754-1281T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795278 | |||||||
| chr12:103795279 | T | C | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.754-1282A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795279 | |||||||
| chr12:103795548 | G | C | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.753+1346C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795548 | |||||||
| chr12:103795606 | C | A | 210 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(207): Show |
216 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.753+1288G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795606 | |||||||
| chr12:103795620 | T | A | 1 | a0001c0001t0010g0260 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.753+1274A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795620 | |||||||
| chr12:103795721 | C | T | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.753+1173G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795721 | |||||||
| chr12:103795776 | T | C | 211 | a0001c0001t0007g0142 a0001c0002t0001g0033 a0001c0002t0001g0036 others(208): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.753+1118A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795776 | |||||||
| chr12:103795836 | C | T | 1 | a0001c0004t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.753+1058G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795836 | |||||||
| chr12:103795837 | A | G | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.753+1057T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795837 | |||||||
| chr12:103795868 | A | G | 1 | a0001c0001t0005g0266 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.753+1026T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795868 | |||||||
| chr12:103795908 | A | G | 1 | a0001c0002t0001g0099 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.753+986T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795908 | |||||||
| chr12:103795924 | A | G | 1 | a0001c0005t0004g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.753+970T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795924 | |||||||
| chr12:103795990 | G | A | 10 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.753+904C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103795990 | |||||||
| chr12:103796145 | A | C | 90 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(87): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.753+749T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796145 | |||||||
| chr12:103796221 | C | T | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.753+673G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796221 | |||||||
| chr12:103796242 | C | T | 2 | a0001c0003t0002g0371 a0001c0003t0002g0372 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.753+652G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796242 | |||||||
| chr12:103796243 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.753+651C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796243 | |||||||
| chr12:103796312 | T | C | 5 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0045 others(2): Show |
5 | HG01099.hp2 HG01928.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+582A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796312 | |||||||
| chr12:103796375 | G | A | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.753+519C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796375 | |||||||
| chr12:103796390 | G | A | 1 | a0001c0002t0005g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.753+504C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796390 | |||||||
| chr12:103796403 | G | C | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.753+491C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796403 | |||||||
| chr12:103796605 | C | T | 1 | a0001c0002t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.753+289G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796605 | |||||||
| chr12:103796679 | C | T | 1 | a0001c0002t0001g0115 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.753+215G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796679 | |||||||
| chr12:103796745 | G | A | 319 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0190 others(316): Show |
328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.753+149C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 6/13 | chr12 | 103796745 | |||||||
| chr12:103797076 | C | T | 92 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.616-45G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797076 | |||||||
| chr12:103797077 | A | G | 148 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.616-46T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797077 | |||||||
| chr12:103797091 | C | T | 62 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.616-60G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797091 | |||||||
| chr12:103797296 | C | A | 2 | a0001c0002t0024g0329 a0001c0002t0050g0330 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.616-265G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797296 | |||||||
| chr12:103797331 | C | T | 1 | a0001c0005t0007g0193 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.616-300G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797331 | |||||||
| chr12:103797374 | G | A | 56 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.616-343C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797374 | |||||||
| chr12:103797385 | G | A | 1 | a0001c0003t0002g0355 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.616-354C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797385 | |||||||
| chr12:103797418 | G | A | 62 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.616-387C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797418 | |||||||
| chr12:103797439 | C | A | 49 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(46): Show |
50 | HG00323.hp1 HG01081.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.616-408G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797439 | |||||||
| chr12:103797470 | TA | T | 12 | a0001c0001t0005g0232 a0001c0001t0005g0266 a0001c0001t0026g0233 others(9): Show |
12 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.616-440delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797470 | |||||||
| chr12:103797470 | TAA | T | 142 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(139): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.616-441_616-440del others(2): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797470 | |||||||
| chr12:103797504 | G | C | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.616-473C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797504 | |||||||
| chr12:103797590 | T | A | 1 | a0001c0004t0003g0208 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.616-559A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797590 | |||||||
| chr12:103797762 | G | C | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.616-731C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797762 | |||||||
| chr12:103797784 | G | A | 1 | a0001c0001t0034g0274 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.616-753C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797784 | |||||||
| chr12:103797918 | A | G | 62 | a0001c0003t0002g0007 a0001c0003t0002g0037 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.615+669T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103797918 | |||||||
| chr12:103798582 | A | G | 1 | a0001c0002t0005g0188 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.615+5T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 5/13 | chr12 | 103798582 | |||||||
| chr12:103798728 | A | G | 39 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(36): Show |
41 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.525-51T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798728 | |||||||
| chr12:103798753 | G | A | 1 | a0001c0004t0003g0219 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.525-76C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798753 | |||||||
| chr12:103798769 | G | A | 4 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-92C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798769 | |||||||
| chr12:103798827 | T | C | 1 | a0001c0002t0023g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.525-150A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798827 | |||||||
| chr12:103798851 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-174G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798851 | |||||||
| chr12:103798920 | A | T | 1 | a0001c0004t0003g0021 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.525-243T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798920 | |||||||
| chr12:103798982 | C | T | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.525-305G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103798982 | |||||||
| chr12:103799015 | G | T | 39 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(36): Show |
41 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.525-338C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799015 | |||||||
| chr12:103799046 | C | G | 148 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(145): Show |
153 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.525-369G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799046 | |||||||
| chr12:103799096 | C | T | 1 | a0001c0003t0008g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.525-419G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799096 | |||||||
| chr12:103799102 | G | A | 56 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0329 others(53): Show |
58 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.525-425C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799102 | |||||||
| chr12:103799156 | G | C | 45 | a0001c0002t0005g0188 a0001c0004t0003g0006 a0001c0004t0003g0020 others(42): Show |
46 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(43): Show |
intron_variant | MODIFIER | c.525-479C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799156 | |||||||
| chr12:103799198 | G | A | 3 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 |
3 | HG01891.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525-521C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799198 | |||||||
| chr12:103799208 | G | C | 15 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0004t0003g0078 others(12): Show |
15 | HG00544.hp2 NA18942.hp1 NA18946.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-531C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799208 | |||||||
| chr12:103799308 | T | C | 65 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0037 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.525-631A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799308 | |||||||
| chr12:103799493 | C | G | 92 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.525-816G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799493 | |||||||
| chr12:103799560 | T | C | 1 | a0001c0003t0018g0369 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.525-883A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799560 | |||||||
| chr12:103799567 | T | G | 2 | a0001c0004t0003g0100 a0001c0004t0003g0101 |
2 | HG00438.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.525-890A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799567 | |||||||
| chr12:103799804 | C | CAAAAAAA others(4): Show |
87 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(84): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.525-1138_525-1128d others(13): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799804 | |||||||
| chr12:103799804 | C | CAAAAAAA others(5): Show |
4 | a0001c0002t0001g0196 a0001c0002t0001g0297 a0001c0002t0006g0173 others(1): Show |
4 | HG00544.hp1 HG01106.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.525-1139_525-1128d others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799804 | |||||||
| chr12:103799804 | CA | C | 137 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(134): Show |
140 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.525-1128delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799804 | |||||||
| chr12:103799805 | A | AAAAAAAA others(5): Show |
3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.525-1129_525-1128i others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799805 | |||||||
| chr12:103799805 | A | AAAAAAAA others(4): Show |
53 | a0001c0002t0001g0094 a0001c0002t0001g0291 a0001c0002t0005g0188 others(50): Show |
55 | HG00438.hp1 HG00544.hp2 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.525-1129_525-1128i others(13): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799805 | |||||||
| chr12:103799806 | A | AAAAAAAA others(3): Show |
1 | a0001c0004t0003g0152 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.525-1130_525-1129i others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799806 | |||||||
| chr12:103799934 | C | T | 2 | a0001c0001t0004g0228 a0001c0001t0033g0229 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.525-1257G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103799934 | |||||||
| chr12:103800134 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-1457G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800134 | |||||||
| chr12:103800162 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-1485C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800162 | |||||||
| chr12:103800370 | C | T | 3 | a0001c0001t0005g0272 a0001c0001t0014g0185 a0001c0001t0014g0336 |
3 | HG01099.hp1 HG02257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.525-1693G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800370 | |||||||
| chr12:103800393 | G | A | 1 | a0001c0005t0004g0042 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.525-1716C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800393 | |||||||
| chr12:103800485 | A | G | 65 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0037 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.525-1808T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800485 | |||||||
| chr12:103800640 | T | C | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.525-1963A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800640 | |||||||
| chr12:103800677 | T | C | 2 | a0001c0001t0034g0162 a0001c0001t0034g0274 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.525-2000A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800677 | |||||||
| chr12:103800810 | C | G | 1 | a0001c0003t0019g0177 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.525-2133G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800810 | |||||||
| chr12:103800813 | T | G | 39 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(36): Show |
39 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.525-2136A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800813 | |||||||
| chr12:103800863 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-2186C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800863 | |||||||
| chr12:103800868 | A | G | 1 | a0001c0006t0012g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.525-2191T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800868 | |||||||
| chr12:103800947 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-2270C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103800947 | |||||||
| chr12:103801046 | T | G | 1 | a0001c0002t0006g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.525-2369A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801046 | |||||||
| chr12:103801067 | G | A | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525-2390C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801067 | |||||||
| chr12:103801079 | C | G | 146 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(143): Show |
151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.525-2402G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801079 | |||||||
| chr12:103801128 | A | C | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525-2451T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801128 | |||||||
| chr12:103801309 | T | C | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.525-2632A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801309 | |||||||
| chr12:103801372 | C | CCTTTTTT others(3): Show |
1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.525-2696_525-2695i others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | C | CT | 69 | a0001c0001t0004g0008 a0001c0001t0004g0184 a0001c0001t0004g0277 others(66): Show |
70 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.525-2696dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | C | CTT | 6 | a0001c0001t0035g0337 a0001c0003t0002g0169 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 HG02257.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-2697_525-2696d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0024g0331 a0001c0002t0024g0332 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.525-2709_525-2696d others(16): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | CT | C | 19 | a0001c0001t0009g0240 a0001c0001t0009g0271 a0001c0001t0009g0334 others(16): Show |
19 | HG01993.hp1 HG02486.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-2696delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | CTTTTT | C | 9 | a0001c0002t0001g0067 a0001c0002t0001g0073 a0001c0002t0001g0148 others(6): Show |
9 | HG00639.hp1 HG01109.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.525-2700_525-2696d others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | CTTTTTT | C | 80 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(77): Show |
83 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.525-2701_525-2696d others(8): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.525-2705_525-2696d others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801372 | CTTTTTTT others(5): Show |
C | 1 | a0001c0006t0012g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.525-2707_525-2696d others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801372 | |||||||
| chr12:103801401 | G | A | 1 | a0001c0004t0017g0150 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.525-2724C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801401 | |||||||
| chr12:103801405 | C | T | 3 | a0001c0001t0014g0153 a0001c0001t0014g0185 a0001c0001t0014g0336 |
3 | HG02257.hp1 HG02895.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.525-2728G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801405 | |||||||
| chr12:103801625 | C | T | 5 | a0001c0003t0002g0007 a0001c0003t0002g0123 a0001c0003t0002g0124 others(2): Show |
6 | HG00609.hp1 NA18941.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.525-2948G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801625 | |||||||
| chr12:103801662 | C | T | 27 | a0001c0001t0009g0239 a0001c0001t0009g0240 a0001c0001t0009g0271 others(24): Show |
28 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.525-2985G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801662 | |||||||
| chr12:103801793 | A | G | 301 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(298): Show |
310 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.525-3116T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103801793 | |||||||
| chr12:103802227 | T | G | 15 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0004t0003g0078 others(12): Show |
15 | HG00544.hp2 NA18942.hp1 NA18946.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-3550A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802227 | |||||||
| chr12:103802311 | G | T | 1 | a0001c0003t0065g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.525-3634C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802311 | |||||||
| chr12:103802353 | G | A | 4 | a0001c0002t0001g0297 a0001c0002t0001g0298 a0001c0002t0001g0299 others(1): Show |
4 | NA18959.hp2 NA18989.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.525-3676C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802353 | |||||||
| chr12:103802359 | A | G | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-3682T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802359 | |||||||
| chr12:103802381 | C | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.525-3704G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802381 | |||||||
| chr12:103802443 | A | C | 213 | a0001c0001t0007g0142 a0001c0001t0035g0181 a0001c0001t0035g0337 others(210): Show |
219 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.525-3766T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802443 | |||||||
| chr12:103802468 | G | A | 1 | a0001c0001t0030g0255 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.525-3791C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802468 | |||||||
| chr12:103802526 | G | A | 142 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(139): Show |
146 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.524+3796C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802526 | |||||||
| chr12:103802576 | G | A | 46 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(43): Show |
47 | HG00323.hp1 HG01081.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.524+3746C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802576 | |||||||
| chr12:103802723 | G | T | 18 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(15): Show |
18 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.524+3599C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802723 | |||||||
| chr12:103802924 | A | G | 2 | a0001c0001t0034g0162 a0001c0001t0034g0274 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.524+3398T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802924 | |||||||
| chr12:103802956 | T | C | 92 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.524+3366A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103802956 | |||||||
| chr12:103803149 | C | G | 3 | a0001c0003t0002g0097 a0001c0003t0002g0098 a0001c0003t0002g0287 |
3 | HG02056.hp1 NA19011.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.524+3173G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803149 | |||||||
| chr12:103803236 | GA | G | 63 | a0001c0001t0005g0048 a0001c0003t0002g0007 a0001c0003t0002g0037 others(60): Show |
64 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.524+3085delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803236 | |||||||
| chr12:103803253 | T | C | 3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.524+3069A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803253 | |||||||
| chr12:103803257 | A | G | 52 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0331 others(49): Show |
53 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(50): Show |
intron_variant | MODIFIER | c.524+3065T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803257 | |||||||
| chr12:103803365 | G | A | 63 | a0001c0001t0005g0048 a0001c0003t0002g0007 a0001c0003t0002g0037 others(60): Show |
64 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.524+2957C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803365 | |||||||
| chr12:103803374 | T | A | 18 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(15): Show |
18 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.524+2948A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803374 | |||||||
| chr12:103803452 | A | G | 1 | a0001c0001t0009g0347 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.524+2870T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803452 | |||||||
| chr12:103803536 | G | T | 6 | a0001c0003t0002g0169 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.524+2786C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803536 | |||||||
| chr12:103803745 | G | A | 63 | a0001c0001t0005g0048 a0001c0003t0002g0007 a0001c0003t0002g0037 others(60): Show |
64 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.524+2577C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803745 | |||||||
| chr12:103803834 | T | C | 1 | a0001c0001t0022g0046 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.524+2488A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803834 | |||||||
| chr12:103803850 | T | C | 1 | a0001c0003t0063g0189 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.524+2472A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803850 | |||||||
| chr12:103803859 | A | AC | 38 | a0001c0001t0004g0278 a0001c0001t0005g0110 a0001c0001t0005g0112 others(35): Show |
40 | HG00323.hp1 HG01081.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.524+2462dupG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803859 | |||||||
| chr12:103803859 | A | ACC | 48 | a0001c0001t0005g0025 a0001c0001t0005g0029 a0001c0001t0005g0044 others(45): Show |
49 | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.524+2461_524+2462d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803859 | |||||||
| chr12:103803859 | A | G | 144 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(141): Show |
148 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.524+2463T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803859 | |||||||
| chr12:103803868 | CCA | C | 133 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(130): Show |
137 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.524+2452_524+2453d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803868 | |||||||
| chr12:103803869 | CA | C | 72 | a0001c0001t0005g0048 a0001c0002t0001g0107 a0001c0002t0001g0116 others(69): Show |
73 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.524+2452delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803869 | |||||||
| chr12:103803870 | A | C | 1 | a0003c0010t0002g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.524+2452T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803870 | |||||||
| chr12:103803918 | G | T | 6 | a0001c0003t0002g0037 a0001c0003t0002g0051 a0001c0003t0002g0061 others(3): Show |
6 | HG01123.hp1 HG02132.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.524+2404C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803918 | |||||||
| chr12:103803927 | C | T | 52 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0331 others(49): Show |
53 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(50): Show |
intron_variant | MODIFIER | c.524+2395G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803927 | |||||||
| chr12:103803975 | A | G | 1 | a0001c0003t0002g0097 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.524+2347T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103803975 | |||||||
| chr12:103804011 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.524+2311C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804011 | |||||||
| chr12:103804104 | G | A | 1 | a0001c0001t0004g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.524+2218C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804104 | |||||||
| chr12:103804194 | C | G | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+2128G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804194 | |||||||
| chr12:103804340 | G | T | 89 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(86): Show |
92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.524+1982C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804340 | |||||||
| chr12:103804518 | C | T | 2 | a0001c0001t0014g0153 a0001c0006t0020g0155 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.524+1804G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804518 | |||||||
| chr12:103804560 | T | A | 5 | a0001c0002t0001g0099 a0001c0002t0024g0329 a0001c0002t0025g0009 others(2): Show |
6 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+1762A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804560 | |||||||
| chr12:103804648 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.524+1674C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804648 | |||||||
| chr12:103804789 | C | T | 10 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(7): Show |
11 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.524+1533G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804789 | |||||||
| chr12:103804906 | C | A | 1 | a0001c0001t0035g0337 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.524+1416G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804906 | |||||||
| chr12:103804927 | T | A | 1 | a0001c0005t0077g0314 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.524+1395A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103804927 | |||||||
| chr12:103805055 | A | G | 2 | a0001c0001t0030g0108 a0001c0001t0030g0255 |
2 | HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.524+1267T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805055 | |||||||
| chr12:103805057 | C | CA | 91 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0037g0335 others(88): Show |
94 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.524+1264dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805057 | |||||||
| chr12:103805057 | C | CAAA | 52 | a0001c0002t0001g0094 a0001c0002t0005g0188 a0001c0002t0024g0331 others(49): Show |
53 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(50): Show |
intron_variant | MODIFIER | c.524+1262_524+1264d others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805057 | |||||||
| chr12:103805228 | T | C | 1 | a0001c0002t0001g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.524+1094A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805228 | |||||||
| chr12:103805292 | A | C | 42 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(39): Show |
44 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.524+1030T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805292 | |||||||
| chr12:103805319 | G | A | 21 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(18): Show |
22 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.524+1003C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805319 | |||||||
| chr12:103805845 | C | CA | 8 | a0001c0001t0004g0190 a0001c0001t0004g0227 a0001c0001t0037g0351 others(5): Show |
8 | HG00738.hp2 HG00741.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.524+476dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805845 | |||||||
| chr12:103805845 | CA | C | 140 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(137): Show |
145 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.524+476delT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805845 | |||||||
| chr12:103805845 | CAA | C | 143 | a0001c0001t0004g0031 a0001c0001t0005g0235 a0001c0001t0005g0323 others(140): Show |
147 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.524+475_524+476del others(2): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805845 | |||||||
| chr12:103805929 | C | T | 63 | a0001c0003t0002g0007 a0001c0003t0002g0051 a0001c0003t0002g0060 others(60): Show |
64 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.524+393G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103805929 | |||||||
| chr12:103806291 | G | A | 1 | a0001c0002t0001g0107 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.524+31C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 4/13 | chr12 | 103806291 | |||||||
| chr12:103806398 | G | A | 2 | a0001c0001t0005g0113 a0001c0001t0039g0344 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.469-21C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 3/13 | chr12 | 103806398 | |||||||
| chr12:103806583 | A | G | 9 | a0001c0001t0005g0029 a0001c0001t0005g0050 a0001c0001t0005g0052 others(6): Show |
9 | HG01975.hp2 HG01981.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.469-206T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 3/13 | chr12 | 103806583 | |||||||
| chr12:103806682 | T | C | 146 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.468+173A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 3/13 | chr12 | 103806682 | |||||||
| chr12:103806819 | C | A | 1 | a0001c0009t0003g0216 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.468+36G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 3/13 | chr12 | 103806819 | |||||||
| chr12:103806836 | A | G | 1 | a0001c0001t0004g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.468+19T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 3/13 | chr12 | 103806836 | |||||||
| chr12:103807275 | C | T | 1 | a0001c0001t0009g0345 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394-346G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103807275 | |||||||
| chr12:103807291 | C | G | 1 | a0001c0001t0009g0345 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394-362G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103807291 | |||||||
| chr12:103807487 | C | A | 1 | a0001c0002t0001g0364 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.394-558G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103807487 | |||||||
| chr12:103807798 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.394-869G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103807798 | |||||||
| chr12:103807904 | A | C | 146 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.394-975T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103807904 | |||||||
| chr12:103808151 | G | A | 143 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(140): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.394-1222C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808151 | |||||||
| chr12:103808382 | C | T | 62 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.394-1453G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808382 | |||||||
| chr12:103808670 | A | G | 1 | a0001c0002t0005g0188 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.394-1741T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808670 | |||||||
| chr12:103808749 | G | A | 1 | a0001c0004t0052g0343 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.394-1820C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808749 | |||||||
| chr12:103808760 | A | G | 349 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(346): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.394-1831T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808760 | |||||||
| chr12:103808795 | T | C | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-1866A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808795 | |||||||
| chr12:103808913 | C | T | 141 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(138): Show |
145 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.394-1984G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808913 | |||||||
| chr12:103808946 | C | T | 1 | a0001c0002t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2017G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808946 | |||||||
| chr12:103808971 | A | G | 4 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-2042T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103808971 | |||||||
| chr12:103809003 | A | G | 1 | a0001c0002t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2074T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809003 | |||||||
| chr12:103809151 | C | T | 1 | a0001c0001t0075g0294 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.394-2222G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809151 | |||||||
| chr12:103809304 | C | G | 1 | a0001c0001t0004g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.394-2375G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809304 | |||||||
| chr12:103809377 | T | C | 1 | a0001c0006t0020g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-2448A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809377 | |||||||
| chr12:103809382 | A | G | 2 | a0001c0002t0024g0331 a0001c0002t0024g0332 |
2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.394-2453T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809382 | |||||||
| chr12:103809440 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.394-2511G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809440 | |||||||
| chr12:103809542 | AC | A | 3 | a0001c0003t0019g0118 a0001c0003t0019g0119 a0001c0003t0019g0120 |
3 | NA19054.hp2 NA19084.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.394-2614delG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809542 | |||||||
| chr12:103809624 | C | T | 44 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(41): Show |
45 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.394-2695G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809624 | |||||||
| chr12:103809674 | ACAGCACA others(8): Show |
A | 1 | a0001c0002t0047g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.394-2760_394-2746d others(17): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809674 | |||||||
| chr12:103809748 | G | T | 1 | a0001c0001t0075g0294 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.394-2819C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809748 | |||||||
| chr12:103809752 | G | A | 6 | a0001c0003t0002g0169 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-2823C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809752 | |||||||
| chr12:103809837 | G | C | 143 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0010g0075 others(140): Show |
147 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.394-2908C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809837 | |||||||
| chr12:103809942 | C | G | 92 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.394-3013G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103809942 | |||||||
| chr12:103810037 | C | T | 1 | a0001c0002t0001g0251 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-3108G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810037 | |||||||
| chr12:103810051 | GGGCAGTG others(3): Show |
G | 43 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(40): Show |
45 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.394-3132_394-3123d others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810051 | |||||||
| chr12:103810222 | G | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-3293C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810222 | |||||||
| chr12:103810293 | G | A | 43 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(40): Show |
45 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.394-3364C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810293 | |||||||
| chr12:103810413 | G | A | 93 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(90): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.394-3484C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810413 | |||||||
| chr12:103810441 | G | A | 2 | a0001c0001t0009g0347 a0001c0001t0038g0180 |
2 | HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.394-3512C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810441 | |||||||
| chr12:103810550 | G | C | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.394-3621C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810550 | |||||||
| chr12:103810584 | T | C | 1 | a0001c0005t0033g0317 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.394-3655A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810584 | |||||||
| chr12:103810640 | T | G | 6 | a0001c0003t0002g0169 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-3711A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810640 | |||||||
| chr12:103810769 | T | C | 1 | a0001c0002t0001g0340 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.394-3840A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810769 | |||||||
| chr12:103810805 | G | C | 189 | a0001c0001t0004g0031 a0001c0001t0005g0109 a0001c0001t0005g0110 others(186): Show |
194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.394-3876C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810805 | |||||||
| chr12:103810825 | C | T | 1 | a0001c0002t0006g0066 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-3896G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810825 | |||||||
| chr12:103810993 | T | G | 162 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0009g0271 others(159): Show |
167 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.393+3944A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103810993 | |||||||
| chr12:103811052 | C | A | 159 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0009g0271 others(156): Show |
164 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.393+3885G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811052 | |||||||
| chr12:103811256 | A | G | 1 | a0001c0001t0004g0278 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.393+3681T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811256 | |||||||
| chr12:103811292 | G | A | 25 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(22): Show |
25 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.393+3645C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811292 | |||||||
| chr12:103811305 | G | A | 4 | a0001c0001t0014g0153 a0001c0001t0014g0185 a0001c0001t0014g0336 others(1): Show |
4 | HG02257.hp1 HG02895.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+3632C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811305 | |||||||
| chr12:103811322 | G | C | 62 | a0001c0001t0007g0142 a0001c0003t0002g0007 a0001c0003t0002g0051 others(59): Show |
63 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.393+3615C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811322 | |||||||
| chr12:103811399 | C | T | 1 | a0001c0001t0009g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.393+3538G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811399 | |||||||
| chr12:103811458 | G | A | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.393+3479C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811458 | |||||||
| chr12:103811533 | C | G | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+3404G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811533 | |||||||
| chr12:103811585 | A | G | 2 | a0001c0001t0007g0142 a0001c0003t0059g0122 |
2 | NA18945.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.393+3352T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811585 | |||||||
| chr12:103811666 | C | T | 91 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(88): Show |
94 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.393+3271G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811666 | |||||||
| chr12:103811762 | A | C | 29 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(26): Show |
29 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.393+3175T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811762 | |||||||
| chr12:103811917 | G | A | 1 | a0001c0001t0070g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.393+3020C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103811917 | |||||||
| chr12:103812087 | A | G | 3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.393+2850T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812087 | |||||||
| chr12:103812150 | C | T | 93 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(90): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.393+2787G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812150 | |||||||
| chr12:103812314 | G | A | 58 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(55): Show |
59 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.393+2623C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812314 | |||||||
| chr12:103812429 | CATA | C | 3 | a0001c0001t0014g0257 a0001c0006t0012g0256 a0001c0006t0012g0269 |
3 | HG02109.hp1 HG02615.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.393+2505_393+2507d others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812429 | |||||||
| chr12:103812453 | A | G | 1 | a0001c0003t0008g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.393+2484T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812453 | |||||||
| chr12:103812520 | CTCTT | C | 93 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(90): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.393+2413_393+2416d others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812520 | |||||||
| chr12:103812703 | C | G | 1 | a0001c0002t0001g0322 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.393+2234G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812703 | |||||||
| chr12:103812715 | T | C | 29 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(26): Show |
29 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.393+2222A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812715 | |||||||
| chr12:103812929 | A | G | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.393+2008T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812929 | |||||||
| chr12:103812946 | T | C | 1 | a0001c0005t0007g0304 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.393+1991A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103812946 | |||||||
| chr12:103813034 | C | A | 1 | a0001c0003t0063g0189 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.393+1903G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813034 | |||||||
| chr12:103813081 | A | G | 93 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(90): Show |
96 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.393+1856T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813081 | |||||||
| chr12:103813099 | T | C | 5 | a0001c0003t0002g0051 a0001c0003t0002g0061 a0001c0003t0002g0283 others(2): Show |
5 | HG01123.hp1 HG02132.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+1838A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813099 | |||||||
| chr12:103813177 | C | G | 160 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0009g0271 others(157): Show |
165 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.393+1760G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813177 | |||||||
| chr12:103813204 | C | T | 1 | a0001c0002t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.393+1733G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813204 | |||||||
| chr12:103813290 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.393+1647G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813290 | |||||||
| chr12:103813387 | A | G | 1 | a0001c0001t0006g0262 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+1550T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813387 | |||||||
| chr12:103813553 | T | G | 68 | a0001c0001t0009g0271 a0001c0001t0010g0005 a0001c0001t0010g0018 others(65): Show |
70 | HG00438.hp1 HG00544.hp2 HG01081.hp2 others(67): Show |
intron_variant | MODIFIER | c.393+1384A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813553 | |||||||
| chr12:103813564 | A | T | 4 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0004g0228 others(1): Show |
4 | HG02717.hp1 HG03139.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+1373T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813564 | |||||||
| chr12:103813636 | C | T | 59 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(56): Show |
60 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.393+1301G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813636 | |||||||
| chr12:103813685 | C | G | 1 | a0001c0002t0046g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.393+1252G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813685 | |||||||
| chr12:103813702 | C | G | 1 | a0001c0002t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.393+1235G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813702 | |||||||
| chr12:103813813 | C | T | 7 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(4): Show |
8 | HG01496.hp2 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+1124G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813813 | |||||||
| chr12:103813836 | C | A | 1 | a0001c0001t0004g0277 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.393+1101G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813836 | |||||||
| chr12:103813837 | T | G | 1 | a0001c0001t0004g0277 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.393+1100A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813837 | |||||||
| chr12:103813985 | T | C | 6 | a0001c0003t0002g0169 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+952A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103813985 | |||||||
| chr12:103814054 | G | A | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.393+883C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814054 | |||||||
| chr12:103814057 | C | G | 2 | a0001c0003t0002g0367 a0001c0003t0002g0368 |
2 | HG00733.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.393+880G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814057 | |||||||
| chr12:103814086 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.393+851G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814086 | |||||||
| chr12:103814092 | T | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.393+845A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814092 | |||||||
| chr12:103814096 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.393+841G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814096 | |||||||
| chr12:103814097 | G | A | 3 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 |
3 | HG01891.hp1 HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.393+840C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814097 | |||||||
| chr12:103814168 | G | A | 1 | a0001c0003t0019g0120 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.393+769C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814168 | |||||||
| chr12:103814333 | G | A | 115 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0001t0009g0271 others(112): Show |
120 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.393+604C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814333 | |||||||
| chr12:103814358 | G | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.393+579C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814358 | |||||||
| chr12:103814471 | T | A | 24 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(21): Show |
24 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.393+466A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 2/13 | chr12 | 103814471 | |||||||
| chr12:103815194 | A | T | 39 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(36): Show |
41 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.209-73T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815194 | |||||||
| chr12:103815276 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0006g0262 |
2 | HG00639.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.209-155A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815276 | |||||||
| chr12:103815292 | A | T | 1 | a0001c0002t0001g0291 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.209-171T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815292 | |||||||
| chr12:103815356 | C | T | 5 | a0001c0002t0001g0055 a0001c0002t0001g0149 a0001c0002t0001g0290 others(2): Show |
5 | NA18964.hp2 NA18965.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-235G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815356 | |||||||
| chr12:103815473 | G | A | 5 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-352C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815473 | |||||||
| chr12:103815531 | C | T | 1 | a0001c0002t0001g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.209-410G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815531 | |||||||
| chr12:103815595 | T | C | 57 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(54): Show |
58 | HG00438.hp1 HG00544.hp2 HG01891.hp1 others(55): Show |
intron_variant | MODIFIER | c.209-474A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815595 | |||||||
| chr12:103815668 | C | T | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-547G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815668 | |||||||
| chr12:103815752 | G | A | 4 | a0001c0004t0003g0159 a0001c0004t0003g0217 a0001c0004t0003g0218 others(1): Show |
4 | HG02572.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-631C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815752 | |||||||
| chr12:103815782 | G | A | 1 | a0001c0001t0083g0238 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.209-661C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815782 | |||||||
| chr12:103815834 | G | A | 1 | a0001c0002t0001g0322 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.209-713C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815834 | |||||||
| chr12:103815883 | T | C | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-762A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815883 | |||||||
| chr12:103815994 | C | T | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-873G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103815994 | |||||||
| chr12:103816256 | C | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.209-1135G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816256 | |||||||
| chr12:103816272 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.209-1151G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816272 | |||||||
| chr12:103816290 | A | T | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-1169T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816290 | |||||||
| chr12:103816309 | A | G | 1 | a0001c0002t0024g0329 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.209-1188T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816309 | |||||||
| chr12:103816343 | T | C | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-1222A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816343 | |||||||
| chr12:103816462 | A | G | 64 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-1341T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816462 | |||||||
| chr12:103816599 | T | C | 1 | a0001c0002t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.209-1478A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816599 | |||||||
| chr12:103816664 | G | C | 122 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(119): Show |
124 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.209-1543C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816664 | |||||||
| chr12:103816763 | C | T | 4 | a0001c0005t0007g0304 a0001c0005t0007g0320 a0001c0005t0015g0013 others(1): Show |
4 | HG00621.hp1 NA18939.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-1642G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816763 | |||||||
| chr12:103816837 | G | A | 1 | a0001c0001t0037g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.209-1716C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816837 | |||||||
| chr12:103816949 | G | T | 349 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(346): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.209-1828C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816949 | |||||||
| chr12:103816967 | C | CT | 146 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0226 others(143): Show |
150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.209-1847dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816967 | |||||||
| chr12:103816967 | C | CTT | 15 | a0001c0001t0004g0184 a0001c0001t0014g0153 a0001c0001t0014g0185 others(12): Show |
15 | HG01433.hp1 HG02129.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.209-1848_209-1847d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816967 | |||||||
| chr12:103816967 | C | CTTTT | 57 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(54): Show |
58 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.209-1850_209-1847d others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103816967 | |||||||
| chr12:103817051 | AG | A | 66 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(63): Show |
67 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.209-1931delC | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817051 | |||||||
| chr12:103817052 | G | A | 283 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(280): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.209-1931C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817052 | |||||||
| chr12:103817064 | A | G | 1 | a0001c0002t0001g0290 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.209-1943T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817064 | |||||||
| chr12:103817067 | G | A | 1 | a0001c0002t0022g0328 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.209-1946C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817067 | |||||||
| chr12:103817180 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-2059G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817180 | |||||||
| chr12:103817214 | T | C | 1 | a0001c0002t0001g0106 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.209-2093A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817214 | |||||||
| chr12:103817347 | A | G | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2226T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817347 | |||||||
| chr12:103817363 | G | GT | 7 | a0001c0002t0001g0116 a0001c0003t0002g0169 a0001c0003t0002g0172 others(4): Show |
7 | HG02129.hp2 NA18960.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.209-2243dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817363 | |||||||
| chr12:103817364 | T | G | 3 | a0001c0001t0005g0164 a0001c0001t0005g0235 a0001c0001t0005g0236 |
3 | HG02109.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.209-2243A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817364 | |||||||
| chr12:103817462 | T | C | 57 | a0001c0001t0009g0271 a0001c0001t0010g0205 a0001c0001t0034g0162 others(54): Show |
58 | HG00438.hp1 HG00544.hp2 HG01891.hp1 others(55): Show |
intron_variant | MODIFIER | c.209-2341A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817462 | |||||||
| chr12:103817500 | C | A | 64 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-2379G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817500 | |||||||
| chr12:103817605 | A | AT | 365 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(362): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.209-2485dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817605 | |||||||
| chr12:103817662 | G | A | 130 | a0001c0001t0004g0031 a0001c0001t0004g0184 a0001c0001t0005g0109 others(127): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.209-2541C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817662 | |||||||
| chr12:103817676 | T | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-2555A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817676 | |||||||
| chr12:103817713 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-2592G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817713 | |||||||
| chr12:103817790 | AT | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-2670delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817790 | |||||||
| chr12:103817865 | A | C | 4 | a0001c0005t0004g0296 a0001c0005t0004g0353 a0001c0005t0004g0354 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-2744T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817865 | |||||||
| chr12:103817869 | T | C | 1 | a0001c0005t0004g0296 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.209-2748A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817869 | |||||||
| chr12:103817889 | C | A | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209-2768G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103817889 | |||||||
| chr12:103818074 | G | A | 1 | a0001c0001t0027g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209-2953C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818074 | |||||||
| chr12:103818207 | C | A | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-3086G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818207 | |||||||
| chr12:103818453 | G | C | 47 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(45): Show |
intron_variant | MODIFIER | c.209-3332C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818453 | |||||||
| chr12:103818503 | G | GTAGCT | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-3387_209-3383d others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818503 | |||||||
| chr12:103818516 | C | T | 1 | a0001c0002t0001g0094 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.209-3395G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818516 | |||||||
| chr12:103818608 | T | A | 91 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(88): Show |
94 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.209-3487A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818608 | |||||||
| chr12:103818772 | C | G | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-3651G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818772 | |||||||
| chr12:103818780 | G | C | 53 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(50): Show |
53 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.209-3659C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818780 | |||||||
| chr12:103818821 | T | C | 126 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(123): Show |
128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.209-3700A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818821 | |||||||
| chr12:103818853 | G | A | 130 | a0001c0001t0004g0031 a0001c0001t0004g0184 a0001c0001t0005g0109 others(127): Show |
134 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.209-3732C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818853 | |||||||
| chr12:103818887 | G | A | 64 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-3766C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103818887 | |||||||
| chr12:103819113 | A | G | 1 | a0001c0004t0003g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.209-3992T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819113 | |||||||
| chr12:103819128 | G | C | 1 | a0001c0002t0001g0338 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.209-4007C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819128 | |||||||
| chr12:103819264 | G | A | 4 | a0001c0001t0034g0162 a0001c0001t0034g0274 a0001c0001t0037g0335 others(1): Show |
4 | HG02559.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-4143C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819264 | |||||||
| chr12:103819414 | A | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-4293T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819414 | |||||||
| chr12:103819449 | A | G | 1 | a0001c0005t0007g0096 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.209-4328T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819449 | |||||||
| chr12:103819475 | T | C | 2 | a0001c0004t0003g0079 a0001c0004t0003g0080 |
2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.209-4354A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819475 | |||||||
| chr12:103819889 | TTTC | T | 3 | a0001c0001t0005g0164 a0001c0001t0005g0235 a0001c0001t0005g0236 |
3 | HG02109.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.209-4771_209-4769d others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819889 | |||||||
| chr12:103819898 | G | T | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209-4777C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819898 | |||||||
| chr12:103819953 | A | G | 125 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(122): Show |
127 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.209-4832T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103819953 | |||||||
| chr12:103820078 | G | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-4957C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820078 | |||||||
| chr12:103820246 | T | C | 3 | a0001c0002t0040g0187 a0001c0002t0040g0231 a0001c0002t0076g0186 |
3 | HG01496.hp2 HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.209-5125A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820246 | |||||||
| chr12:103820313 | C | T | 59 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(56): Show |
60 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(57): Show |
intron_variant | MODIFIER | c.209-5192G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820313 | |||||||
| chr12:103820529 | C | T | 47 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(45): Show |
intron_variant | MODIFIER | c.209-5408G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820529 | |||||||
| chr12:103820568 | A | T | 5 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-5447T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820568 | |||||||
| chr12:103820714 | G | A | 1 | a0001c0001t0028g0327 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.209-5593C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820714 | |||||||
| chr12:103820934 | T | C | 2 | a0001c0002t0001g0147 a0001c0002t0001g0148 |
2 | HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.209-5813A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103820934 | |||||||
| chr12:103821212 | A | T | 122 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(119): Show |
124 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.209-6091T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821212 | |||||||
| chr12:103821244 | G | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-6123C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821244 | |||||||
| chr12:103821378 | G | C | 1 | a0001c0003t0018g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.209-6257C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821378 | |||||||
| chr12:103821509 | C | T | 1 | a0001c0001t0030g0255 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.209-6388G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821509 | |||||||
| chr12:103821530 | A | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-6409T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821530 | |||||||
| chr12:103821565 | G | C | 1 | a0001c0002t0046g0059 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.209-6444C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103821565 | |||||||
| chr12:103822096 | C | T | 122 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(119): Show |
124 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.209-6975G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822096 | |||||||
| chr12:103822184 | T | TA | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-7064dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822184 | |||||||
| chr12:103822213 | C | A | 47 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(45): Show |
intron_variant | MODIFIER | c.209-7092G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822213 | |||||||
| chr12:103822315 | C | A | 1 | a0001c0004t0056g0081 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.209-7194G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822315 | |||||||
| chr12:103822436 | G | A | 121 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0009g0271 others(118): Show |
123 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.209-7315C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822436 | |||||||
| chr12:103822910 | G | A | 1 | a0001c0001t0037g0351 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.209-7789C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103822910 | |||||||
| chr12:103823000 | A | C | 62 | a0001c0001t0009g0271 a0001c0001t0010g0205 a0001c0001t0034g0162 others(59): Show |
63 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(60): Show |
intron_variant | MODIFIER | c.209-7879T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823000 | |||||||
| chr12:103823115 | A | G | 1 | a0001c0002t0023g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.209-7994T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823115 | |||||||
| chr12:103823200 | T | C | 1 | a0001c0001t0035g0337 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.209-8079A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823200 | |||||||
| chr12:103823224 | C | CA | 47 | a0001c0003t0002g0103 a0001c0005t0004g0041 a0001c0005t0004g0042 others(44): Show |
49 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.209-8104dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823224 | |||||||
| chr12:103823224 | C | CAA | 46 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(43): Show |
47 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.209-8105_209-8104d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823224 | |||||||
| chr12:103823225 | A | T | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | NA19066.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.209-8104T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823225 | |||||||
| chr12:103823276 | A | G | 47 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(45): Show |
intron_variant | MODIFIER | c.209-8155T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823276 | |||||||
| chr12:103823382 | C | A | 2 | a0001c0003t0002g0371 a0001c0003t0002g0372 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.209-8261G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823382 | |||||||
| chr12:103823418 | C | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-8297G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823418 | |||||||
| chr12:103823468 | C | A | 1 | a0001c0001t0009g0326 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.209-8347G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823468 | |||||||
| chr12:103823525 | T | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-8404A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823525 | |||||||
| chr12:103823543 | T | C | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-8422A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823543 | |||||||
| chr12:103823639 | T | C | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-8518A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823639 | |||||||
| chr12:103823777 | A | G | 1 | a0001c0001t0005g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.209-8656T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823777 | |||||||
| chr12:103823822 | C | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-8701G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823822 | |||||||
| chr12:103823857 | C | T | 1 | a0001c0002t0006g0064 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.209-8736G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823857 | |||||||
| chr12:103823873 | G | C | 4 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-8752C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823873 | |||||||
| chr12:103823964 | AGGCTAGG others(5): Show |
A | 2 | a0001c0002t0024g0329 a0001c0002t0050g0330 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.209-8855_209-8844d others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103823964 | |||||||
| chr12:103824021 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-8900G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824021 | |||||||
| chr12:103824032 | T | C | 2 | a0001c0004t0003g0221 a0001c0004t0032g0220 |
2 | NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.209-8911A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824032 | |||||||
| chr12:103824164 | G | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-9043C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824164 | |||||||
| chr12:103824182 | T | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209-9061A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824182 | |||||||
| chr12:103824351 | G | A | 1 | a0001c0006t0012g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.209-9230C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824351 | |||||||
| chr12:103824359 | G | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-9238C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824359 | |||||||
| chr12:103824370 | C | T | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-9249G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824370 | |||||||
| chr12:103824648 | T | A | 60 | a0001c0001t0009g0271 a0001c0001t0010g0205 a0001c0001t0034g0162 others(57): Show |
61 | HG00438.hp1 HG00544.hp2 HG01496.hp2 others(58): Show |
intron_variant | MODIFIER | c.209-9527A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824648 | |||||||
| chr12:103824681 | G | A | 86 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(83): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.209-9560C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824681 | |||||||
| chr12:103824690 | GATGCCAC others(16): Show |
G | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.209-9592_209-9570d others(25): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824690 | |||||||
| chr12:103824820 | G | T | 2 | a0001c0001t0035g0181 a0001c0001t0035g0337 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.209-9699C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824820 | |||||||
| chr12:103824960 | G | A | 45 | a0001c0005t0004g0041 a0001c0005t0004g0042 a0001c0005t0004g0160 others(42): Show |
47 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.209-9839C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103824960 | |||||||
| chr12:103825060 | C | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-9939G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825060 | |||||||
| chr12:103825061 | A | G | 2 | a0001c0001t0034g0162 a0001c0001t0034g0274 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.209-9940T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825061 | |||||||
| chr12:103825075 | G | GC | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-9955dupG | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825075 | |||||||
| chr12:103825082 | C | T | 2 | a0001c0004t0003g0293 a0001c0004t0054g0292 |
2 | NA18954.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.209-9961G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825082 | |||||||
| chr12:103825150 | A | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-10029T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825150 | |||||||
| chr12:103825170 | T | A | 4 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(1): Show |
5 | HG02258.hp1 HG02717.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-10049A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825170 | |||||||
| chr12:103825178 | G | A | 64 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(61): Show |
65 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.209-10057C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825178 | |||||||
| chr12:103825222 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-10101G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825222 | |||||||
| chr12:103825242 | T | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209-10121A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825242 | |||||||
| chr12:103825295 | T | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-10174A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825295 | |||||||
| chr12:103825587 | T | C | 1 | a0001c0002t0006g0032 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.209-10466A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825587 | |||||||
| chr12:103825666 | T | C | 46 | a0001c0005t0004g0041 a0001c0005t0004g0042 a0001c0005t0004g0160 others(43): Show |
48 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.209-10545A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825666 | |||||||
| chr12:103825772 | G | A | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-10651C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825772 | |||||||
| chr12:103825983 | T | C | 1 | a0001c0004t0003g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.209-10862A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103825983 | |||||||
| chr12:103826036 | T | C | 105 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(102): Show |
108 | HG00099.hp2 HG00438.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.209-10915A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826036 | |||||||
| chr12:103826081 | C | G | 42 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(39): Show |
43 | HG00438.hp2 HG00609.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.209-10960G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826081 | |||||||
| chr12:103826099 | T | A | 46 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(43): Show |
49 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.209-10978A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826099 | |||||||
| chr12:103826226 | T | G | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.209-11105A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826226 | |||||||
| chr12:103826256 | A | G | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-11135T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826256 | |||||||
| chr12:103826293 | T | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-11172A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826293 | |||||||
| chr12:103826329 | A | C | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-11208T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826329 | |||||||
| chr12:103826341 | A | G | 2 | a0001c0001t0005g0232 a0001c0001t0026g0233 |
2 | HG01943.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.209-11220T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826341 | |||||||
| chr12:103826433 | G | A | 1 | a0001c0002t0014g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.209-11312C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826433 | |||||||
| chr12:103826479 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-11358G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826479 | |||||||
| chr12:103826651 | G | C | 1 | a0001c0001t0010g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.209-11530C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826651 | |||||||
| chr12:103826692 | T | G | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.209-11571A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826692 | |||||||
| chr12:103826906 | T | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-11785A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826906 | |||||||
| chr12:103826965 | T | C | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-11844A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103826965 | |||||||
| chr12:103827137 | C | A | 91 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(88): Show |
94 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.209-12016G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827137 | |||||||
| chr12:103827137 | C | T | 65 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(62): Show |
66 | HG00438.hp2 HG00609.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.209-12016G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827137 | |||||||
| chr12:103827275 | A | T | 1 | a0001c0005t0007g0225 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.209-12154T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827275 | |||||||
| chr12:103827352 | T | C | 107 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(104): Show |
111 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.209-12231A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827352 | |||||||
| chr12:103827567 | T | G | 1 | a0001c0004t0003g0022 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.209-12446A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827567 | |||||||
| chr12:103827689 | G | A | 44 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(41): Show |
47 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.209-12568C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827689 | |||||||
| chr12:103827945 | C | T | 1 | a0001c0002t0013g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.209-12824G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103827945 | |||||||
| chr12:103828072 | C | T | 307 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(304): Show |
316 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.208+12877G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828072 | |||||||
| chr12:103828082 | A | G | 1 | a0001c0005t0011g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.208+12867T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828082 | |||||||
| chr12:103828126 | T | C | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+12823A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828126 | |||||||
| chr12:103828169 | C | T | 5 | a0001c0001t0009g0345 a0001c0001t0009g0346 a0001c0001t0009g0347 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+12780G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828169 | |||||||
| chr12:103828322 | G | T | 1 | a0001c0001t0004g0190 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.208+12627C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828322 | |||||||
| chr12:103828354 | C | T | 1 | a0001c0006t0012g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.208+12595G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828354 | |||||||
| chr12:103828433 | T | A | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+12516A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828433 | |||||||
| chr12:103828513 | A | G | 3 | a0001c0001t0005g0164 a0001c0001t0005g0235 a0001c0001t0005g0236 |
3 | HG02109.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.208+12436T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828513 | |||||||
| chr12:103828696 | C | CT | 106 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(103): Show |
109 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.208+12252dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828696 | |||||||
| chr12:103828696 | C | CTT | 60 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0005g0056 others(57): Show |
61 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.208+12251_208+1225 others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828696 | |||||||
| chr12:103828702 | A | T | 296 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0005g0004 others(293): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.208+12247T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828702 | |||||||
| chr12:103828715 | G | T | 2 | a0001c0004t0053g0206 a0001c0004t0055g0301 |
2 | NA18992.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.208+12234C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828715 | |||||||
| chr12:103828816 | G | A | 16 | a0001c0003t0002g0063 a0001c0003t0002g0355 a0001c0003t0002g0356 others(13): Show |
16 | HG00733.hp2 HG01070.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.208+12133C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828816 | |||||||
| chr12:103828964 | G | A | 89 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(86): Show |
92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+11985C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103828964 | |||||||
| chr12:103829053 | C | G | 1 | a0001c0005t0011g0243 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.208+11896G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103829053 | |||||||
| chr12:103829600 | T | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.208+11349A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103829600 | |||||||
| chr12:103829804 | T | C | 5 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+11145A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103829804 | |||||||
| chr12:103829884 | A | G | 24 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(21): Show |
24 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.208+11065T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103829884 | |||||||
| chr12:103829885 | G | GA | 170 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(167): Show |
174 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.208+11063dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103829885 | |||||||
| chr12:103830093 | G | A | 2 | a0001c0003t0002g0285 a0001c0003t0018g0137 |
2 | NA18969.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.208+10856C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103830093 | |||||||
| chr12:103830101 | C | T | 1 | a0001c0002t0006g0357 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+10848G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103830101 | |||||||
| chr12:103830353 | T | A | 1 | a0001c0001t0004g0264 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.208+10596A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103830353 | |||||||
| chr12:103830506 | G | C | 96 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(93): Show |
99 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.208+10443C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103830506 | |||||||
| chr12:103830520 | C | T | 96 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(93): Show |
99 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.208+10429G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103830520 | |||||||
| chr12:103831080 | G | A | 56 | a0001c0002t0001g0033 a0001c0002t0001g0036 a0001c0002t0001g0038 others(53): Show |
58 | HG00544.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.208+9869C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831080 | |||||||
| chr12:103831163 | T | C | 5 | a0001c0002t0001g0055 a0001c0002t0001g0149 a0001c0002t0001g0290 others(2): Show |
5 | NA18964.hp2 NA18965.hp1 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+9786A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831163 | |||||||
| chr12:103831392 | G | A | 34 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(31): Show |
36 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.208+9557C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831392 | |||||||
| chr12:103831506 | C | T | 89 | a0001c0001t0004g0031 a0001c0001t0005g0323 a0001c0002t0001g0033 others(86): Show |
92 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+9443G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831506 | |||||||
| chr12:103831511 | C | G | 303 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(300): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.208+9438G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831511 | |||||||
| chr12:103831531 | C | A | 1 | a0001c0001t0070g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.208+9418G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831531 | |||||||
| chr12:103831563 | C | T | 39 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(36): Show |
41 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.208+9386G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831563 | |||||||
| chr12:103831655 | G | A | 1 | a0001c0002t0006g0357 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+9294C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831655 | |||||||
| chr12:103831755 | G | A | 2 | a0001c0003t0008g0138 a0001c0003t0008g0141 |
2 | NA18959.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.208+9194C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831755 | |||||||
| chr12:103831769 | T | C | 1 | a0001c0002t0022g0328 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.208+9180A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831769 | |||||||
| chr12:103831770 | C | CT | 8 | a0001c0002t0001g0154 a0001c0002t0001g0246 a0001c0002t0001g0251 others(5): Show |
8 | HG02258.hp2 HG02738.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+9178dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831770 | |||||||
| chr12:103831770 | CT | C | 114 | a0001c0001t0004g0031 a0001c0001t0004g0184 a0001c0001t0005g0052 others(111): Show |
115 | HG00280.hp1 HG00323.hp1 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.208+9178delA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831770 | |||||||
| chr12:103831770 | CTTTTT | C | 94 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(91): Show |
97 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.208+9174_208+9178d others(7): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831770 | |||||||
| chr12:103831841 | T | A | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+9108A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831841 | |||||||
| chr12:103831864 | T | C | 304 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(301): Show |
313 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.208+9085A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103831864 | |||||||
| chr12:103832028 | C | T | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.208+8921G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832028 | |||||||
| chr12:103832059 | G | A | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.208+8890C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832059 | |||||||
| chr12:103832254 | C | A | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8695G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832254 | |||||||
| chr12:103832360 | T | G | 68 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0007g0142 others(65): Show |
69 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.208+8589A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832360 | |||||||
| chr12:103832364 | A | C | 47 | a0001c0002t0001g0191 a0001c0002t0005g0188 a0001c0002t0046g0059 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG02015.hp1 others(45): Show |
intron_variant | MODIFIER | c.208+8585T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832364 | |||||||
| chr12:103832428 | C | T | 67 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0039g0030 others(64): Show |
68 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+8521G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832428 | |||||||
| chr12:103832485 | C | A | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8464G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832485 | |||||||
| chr12:103832502 | A | G | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8447T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832502 | |||||||
| chr12:103832503 | T | A | 10 | a0001c0001t0004g0190 a0001c0001t0004g0223 a0001c0001t0004g0265 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+8446A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832503 | |||||||
| chr12:103832511 | TCTC | T | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8435_208+8437d others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832511 | |||||||
| chr12:103832562 | T | G | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8387A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832562 | |||||||
| chr12:103832659 | A | G | 5 | a0001c0001t0004g0184 a0001c0001t0014g0153 a0001c0001t0014g0185 others(2): Show |
5 | HG02257.hp1 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+8290T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832659 | |||||||
| chr12:103832807 | GCGTAACA others(23): Show |
G | 1 | a0001c0004t0003g0020 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.208+8112_208+8141d others(32): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832807 | |||||||
| chr12:103832857 | T | G | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+8092A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103832857 | |||||||
| chr12:103833014 | G | A | 4 | a0001c0002t0001g0156 a0001c0002t0001g0203 a0001c0002t0001g0204 others(1): Show |
4 | HG00621.hp2 NA18939.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+7935C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833014 | |||||||
| chr12:103833142 | G | T | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+7807C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833142 | |||||||
| chr12:103833192 | G | A | 1 | a0001c0002t0023g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.208+7757C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833192 | |||||||
| chr12:103833205 | G | A | 11 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(8): Show |
12 | HG01081.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.208+7744C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833205 | |||||||
| chr12:103833238 | A | G | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+7711T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833238 | |||||||
| chr12:103833315 | A | G | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+7634T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833315 | |||||||
| chr12:103833379 | T | G | 2 | a0001c0002t0024g0329 a0001c0002t0050g0330 |
2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.208+7570A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833379 | |||||||
| chr12:103833451 | ATTATATA others(28): Show |
A | 1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+7463_208+7497d others(37): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833451 | |||||||
| chr12:103833495 | G | A | 88 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(85): Show |
91 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.208+7454C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833495 | |||||||
| chr12:103833603 | C | T | 1 | a0001c0001t0004g0031 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.208+7346G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833603 | |||||||
| chr12:103833663 | C | CCCCAGCC others(58): Show |
1 | a0001c0004t0003g0020 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.208+7221_208+7285d others(67): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833663 | |||||||
| chr12:103833719 | G | GA | 183 | a0001c0001t0004g0031 a0001c0001t0005g0109 a0001c0001t0005g0110 others(180): Show |
188 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.208+7229dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833719 | |||||||
| chr12:103833719 | G | GAA | 7 | a0001c0001t0004g0184 a0001c0001t0010g0260 a0001c0001t0014g0153 others(4): Show |
7 | HG01981.hp1 HG02055.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+7228_208+7229d others(4): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833719 | |||||||
| chr12:103833780 | G | C | 1 | a0001c0001t0009g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.208+7169C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833780 | |||||||
| chr12:103833821 | A | C | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+7128T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833821 | |||||||
| chr12:103833822 | G | C | 97 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(94): Show |
100 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.208+7127C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833822 | |||||||
| chr12:103833874 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.208+7075G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833874 | |||||||
| chr12:103833883 | A | G | 5 | a0001c0001t0005g0054 a0001c0001t0005g0232 a0001c0001t0005g0234 others(2): Show |
5 | HG00099.hp2 HG01074.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+7066T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833883 | |||||||
| chr12:103833953 | T | G | 7 | a0001c0002t0024g0329 a0001c0002t0025g0009 a0001c0002t0025g0280 others(4): Show |
8 | HG01496.hp2 HG02258.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+6996A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103833953 | |||||||
| chr12:103834066 | C | T | 90 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(87): Show |
93 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.208+6883G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834066 | |||||||
| chr12:103834645 | A | G | 1 | a0001c0001t0030g0108 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.208+6304T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834645 | |||||||
| chr12:103834654 | C | A | 90 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(87): Show |
93 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.208+6295G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834654 | |||||||
| chr12:103834698 | A | T | 89 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(86): Show |
92 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.208+6251T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834698 | |||||||
| chr12:103834795 | G | T | 95 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(92): Show |
98 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.208+6154C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834795 | |||||||
| chr12:103834799 | C | T | 3 | a0001c0001t0004g0223 a0001c0001t0036g0222 a0001c0001t0072g0224 |
3 | HG02145.hp1 HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.208+6150G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834799 | |||||||
| chr12:103834940 | G | A | 54 | a0001c0001t0009g0271 a0001c0001t0034g0162 a0001c0001t0034g0274 others(51): Show |
55 | HG00438.hp1 HG00544.hp2 HG01891.hp1 others(52): Show |
intron_variant | MODIFIER | c.208+6009C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103834940 | |||||||
| chr12:103835002 | T | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.208+5947A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835002 | |||||||
| chr12:103835047 | G | A | 1 | a0001c0002t0016g0040 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.208+5902C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835047 | |||||||
| chr12:103835186 | C | T | 1 | a0001c0004t0003g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.208+5763G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835186 | |||||||
| chr12:103835193 | T | C | 1 | a0001c0002t0001g0154 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.208+5756A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835193 | |||||||
| chr12:103835199 | C | T | 4 | a0001c0002t0001g0094 a0001c0002t0024g0331 a0001c0002t0024g0332 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+5750G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835199 | |||||||
| chr12:103835309 | C | G | 2 | a0001c0006t0012g0167 a0001c0006t0012g0168 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.208+5640G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835309 | |||||||
| chr12:103835392 | C | T | 1 | a0001c0001t0038g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.208+5557G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835392 | |||||||
| chr12:103835441 | T | G | 2 | a0001c0003t0002g0365 a0001c0003t0002g0366 |
2 | HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.208+5508A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835441 | |||||||
| chr12:103835477 | G | A | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.208+5472C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835477 | |||||||
| chr12:103835634 | A | G | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.208+5315T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835634 | |||||||
| chr12:103835725 | C | T | 40 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(37): Show |
42 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.208+5224G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835725 | |||||||
| chr12:103835990 | G | A | 1 | a0001c0001t0037g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.208+4959C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835990 | |||||||
| chr12:103835995 | C | T | 1 | a0001c0002t0001g0191 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.208+4954G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103835995 | |||||||
| chr12:103836050 | T | A | 6 | a0001c0002t0006g0173 a0001c0003t0002g0172 a0001c0003t0019g0177 others(3): Show |
6 | NA18960.hp2 NA18977.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+4899A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836050 | |||||||
| chr12:103836292 | C | G | 38 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(35): Show |
40 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.208+4657G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836292 | |||||||
| chr12:103836431 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208+4518C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836431 | |||||||
| chr12:103836522 | T | A | 1 | a0001c0002t0001g0151 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.208+4427A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836522 | |||||||
| chr12:103836671 | C | CT | 31 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(28): Show |
33 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.208+4277dupA | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836671 | |||||||
| chr12:103836685 | G | A | 69 | a0001c0001t0010g0005 a0001c0001t0010g0018 a0001c0001t0010g0074 others(66): Show |
71 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.208+4264C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836685 | |||||||
| chr12:103836721 | C | T | 30 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(27): Show |
32 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.208+4228G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836721 | |||||||
| chr12:103836829 | G | A | 23 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0001t0005g0112 others(20): Show |
23 | HG00323.hp1 HG01099.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.208+4120C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836829 | |||||||
| chr12:103836894 | G | A | 1 | a0001c0006t0020g0155 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.208+4055C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836894 | |||||||
| chr12:103836923 | G | A | 71 | a0001c0001t0004g0190 a0001c0001t0010g0005 a0001c0001t0010g0018 others(68): Show |
73 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.208+4026C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836923 | |||||||
| chr12:103836951 | G | A | 5 | a0001c0001t0009g0271 a0001c0001t0037g0335 a0001c0001t0037g0351 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+3998C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836951 | |||||||
| chr12:103836973 | C | T | 5 | a0001c0001t0009g0271 a0001c0001t0037g0335 a0001c0001t0037g0351 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+3976G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836973 | |||||||
| chr12:103836975 | A | C | 303 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0184 others(300): Show |
312 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.208+3974T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103836975 | |||||||
| chr12:103837117 | G | A | 30 | a0001c0001t0001g0085 a0001c0001t0005g0004 a0001c0001t0005g0024 others(27): Show |
32 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.208+3832C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837117 | |||||||
| chr12:103837361 | T | A | 1 | a0001c0001t0070g0237 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.208+3588A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837361 | |||||||
| chr12:103837473 | G | A | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.208+3476C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837473 | |||||||
| chr12:103837544 | T | C | 1 | a0001c0002t0006g0357 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+3405A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837544 | |||||||
| chr12:103837545 | C | T | 1 | a0001c0002t0006g0357 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.208+3404G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837545 | |||||||
| chr12:103837573 | TTCCACCA others(58): Show |
T | 1 | a0001c0004t0003g0021 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208+3311_208+3375d others(67): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103837573 | |||||||
| chr12:103838018 | T | C | 1 | a0001c0001t0027g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208+2931A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838018 | |||||||
| chr12:103838023 | A | G | 1 | a0001c0001t0034g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.208+2926T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838023 | |||||||
| chr12:103838035 | G | GCCTCAGA others(28): Show |
1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+2879_208+2913d others(37): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838035 | |||||||
| chr12:103838062 | A | G | 1 | a0001c0002t0001g0273 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.208+2887T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838062 | |||||||
| chr12:103838067 | T | C | 10 | a0001c0001t0009g0239 a0001c0001t0009g0240 a0001c0001t0009g0326 others(7): Show |
10 | HG01167.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+2882A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838067 | |||||||
| chr12:103838081 | C | T | 1 | a0001c0005t0004g0286 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.208+2868G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838081 | |||||||
| chr12:103838118 | C | A | 1 | a0001c0002t0021g0001 | 3 | HG01256.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.208+2831G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838118 | |||||||
| chr12:103838330 | T | C | 1 | a0001c0004t0003g0093 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.208+2619A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838330 | |||||||
| chr12:103838333 | G | A | 7 | a0001c0002t0001g0088 a0001c0003t0002g0087 a0001c0004t0003g0089 others(4): Show |
7 | HG02080.hp2 HG02155.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+2616C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838333 | |||||||
| chr12:103838352 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208+2597C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838352 | |||||||
| chr12:103838402 | C | G | 329 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0082 others(326): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.208+2547G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838402 | |||||||
| chr12:103838495 | A | T | 65 | a0001c0001t0005g0370 a0001c0001t0007g0142 a0001c0002t0001g0147 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.208+2454T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838495 | |||||||
| chr12:103838578 | T | C | 1 | a0001c0002t0049g0350 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.208+2371A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838578 | |||||||
| chr12:103838673 | C | A | 3 | a0001c0002t0001g0094 a0001c0005t0004g0353 a0001c0005t0004g0354 |
3 | HG01891.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+2276G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838673 | |||||||
| chr12:103838702 | G | T | 1 | a0001c0002t0001g0055 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.208+2247C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838702 | |||||||
| chr12:103838726 | TAAAC | T | 3 | a0001c0002t0001g0094 a0001c0005t0004g0353 a0001c0005t0004g0354 |
3 | HG01891.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+2219_208+2222d others(6): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838726 | |||||||
| chr12:103838887 | C | A | 12 | a0001c0001t0006g0245 a0001c0001t0022g0244 a0001c0002t0001g0105 others(9): Show |
12 | HG00140.hp1 HG00642.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+2062G>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838887 | |||||||
| chr12:103838890 | A | G | 101 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0082 others(98): Show |
105 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.208+2059T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838890 | |||||||
| chr12:103838960 | A | G | 335 | a0001c0001t0001g0085 a0001c0001t0004g0031 a0001c0001t0004g0082 others(332): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.208+1989T>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103838960 | |||||||
| chr12:103839306 | T | TTGCAATC others(3): Show |
1 | a0001c0004t0003g0021 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208+1633_208+1642d others(12): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839306 | |||||||
| chr12:103839350 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208+1599C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839350 | |||||||
| chr12:103839599 | T | TA | 10 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0277 others(7): Show |
11 | HG02055.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+1349dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839599 | |||||||
| chr12:103839615 | C | G | 18 | a0001c0001t0005g0370 a0001c0002t0001g0364 a0001c0002t0006g0357 others(15): Show |
18 | HG00733.hp2 HG01070.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+1334G>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839615 | |||||||
| chr12:103839767 | TAAGAAAG others(108): Show |
T | 1 | a0001c0004t0003g0020 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.208+1067_208+1181d others(2): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839767 | |||||||
| chr12:103839871 | C | CA | 5 | a0001c0001t0009g0334 a0001c0001t0039g0344 a0001c0002t0024g0331 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+1077dupT | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839871 | |||||||
| chr12:103839988 | C | T | 21 | a0001c0001t0009g0334 a0001c0001t0009g0345 a0001c0001t0009g0346 others(18): Show |
21 | HG01167.hp1 HG01891.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.208+961G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103839988 | |||||||
| chr12:103840021 | G | C | 1 | a0001c0002t0038g0270 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.208+928C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840021 | |||||||
| chr12:103840092 | G | A | 22 | a0001c0001t0009g0334 a0001c0001t0009g0345 a0001c0001t0009g0346 others(19): Show |
22 | HG01167.hp1 HG01891.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+857C>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840092 | |||||||
| chr12:103840208 | G | C | 57 | a0001c0001t0005g0272 a0001c0001t0005g0323 a0001c0001t0009g0271 others(54): Show |
60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.208+741C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840208 | |||||||
| chr12:103840218 | T | C | 3 | a0001c0002t0001g0094 a0001c0005t0004g0353 a0001c0005t0004g0354 |
3 | HG01891.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+731A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840218 | |||||||
| chr12:103840371 | C | T | 1 | a0001c0002t0045g0026 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.208+578G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840371 | |||||||
| chr12:103840372 | G | GCTCATCT others(286): Show |
1 | a0001c0004t0017g0019 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.208+576_208+577ins others(293): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840372 | |||||||
| chr12:103840372 | G | GCTCATCT others(541): Show |
1 | a0001c0004t0003g0021 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208+576_208+577ins others(548): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840372 | |||||||
| chr12:103840372 | G | GCTCATCT others(706): Show |
1 | a0001c0004t0003g0020 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.208+576_208+577ins others(713): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840372 | |||||||
| chr12:103840374 | A | T | 3 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0004t0017g0019 |
3 | NA18952.hp2 NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.208+575T>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840374 | |||||||
| chr12:103840377 | G | GCTCAGCT others(13): Show |
5 | a0001c0001t0005g0050 a0001c0001t0005g0052 a0001c0001t0005g0054 others(2): Show |
5 | HG01123.hp1 HG01123.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+571_208+572ins others(20): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCAGCT others(23): Show |
1 | a0001c0004t0003g0022 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.208+571_208+572ins others(30): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCAT | 58 | a0001c0001t0005g0164 a0001c0001t0005g0166 a0001c0001t0005g0370 others(55): Show |
59 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.208+567_208+571dup others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCATCT others(3): Show |
29 | a0001c0001t0005g0095 a0001c0001t0005g0109 a0001c0001t0005g0110 others(26): Show |
31 | HG00438.hp1 HG01169.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.208+562_208+571dup others(10): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCATCT others(8): Show |
45 | a0001c0001t0001g0085 a0001c0001t0004g0082 a0001c0001t0005g0056 others(42): Show |
47 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.208+557_208+571dup others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCATCT others(13): Show |
26 | a0001c0001t0004g0031 a0001c0001t0005g0004 a0001c0001t0005g0029 others(23): Show |
28 | HG00280.hp2 HG00609.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.208+552_208+571dup others(20): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | GCTCATCT others(18): Show |
3 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0005t0011g0023 |
3 | HG01928.hp1 HG01978.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.208+547_208+571dup others(25): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | G | T | 3 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0004t0017g0019 |
3 | NA18952.hp2 NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.208+572C>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | GCTCAT | G | 66 | a0001c0001t0004g0275 a0001c0001t0004g0276 a0001c0001t0004g0277 others(63): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.208+567_208+571del others(5): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | GCTCATCT others(3): Show |
G | 6 | a0001c0001t0009g0334 a0001c0002t0024g0329 a0001c0002t0024g0331 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+562_208+571del others(10): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840377 | GCTCATCT others(8): Show |
G | 17 | a0001c0001t0009g0345 a0001c0001t0009g0346 a0001c0001t0009g0347 others(14): Show |
17 | HG01167.hp1 HG01891.hp2 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.208+557_208+571del others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840377 | |||||||
| chr12:103840379 | T | TCATCCCA others(678): Show |
1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+569_208+570ins others(685): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840379 | |||||||
| chr12:103840384 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+565A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840384 | |||||||
| chr12:103840387 | T | G | 1 | a0001c0002t0022g0328 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.208+562A>C | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840387 | |||||||
| chr12:103840389 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+560A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840389 | |||||||
| chr12:103840394 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+555A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840394 | |||||||
| chr12:103840399 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+550A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840399 | |||||||
| chr12:103840404 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+545A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840404 | |||||||
| chr12:103840408 | CTCATCTC others(8): Show |
C | 1 | a0001c0002t0001g0352 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.208+526_208+540del others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840408 | |||||||
| chr12:103840409 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+540A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840409 | |||||||
| chr12:103840414 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+535A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840414 | |||||||
| chr12:103840419 | T | C | 1 | a0001c0005t0004g0354 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.208+530A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840419 | |||||||
| chr12:103840419 | T | TCATCTCA others(688): Show |
1 | a0001c0005t0004g0353 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.208+529_208+530ins others(695): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840419 | |||||||
| chr12:103840421 | A | ATCTCATC others(13): Show |
2 | a0001c0001t0005g0176 a0001c0006t0020g0175 |
2 | HG00323.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.208+527_208+528ins others(20): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840421 | |||||||
| chr12:103840421 | A | ATCTCATC others(8): Show |
3 | a0001c0002t0006g0170 a0001c0006t0012g0167 a0001c0006t0012g0168 |
3 | HG03491.hp2 HG03492.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.208+527_208+528ins others(15): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840421 | |||||||
| chr12:103840422 | T | A | 2 | a0001c0002t0001g0291 a0001c0002t0022g0328 |
2 | HG01516.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.208+527A>T | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840422 | |||||||
| chr12:103840422 | T | TCTCATCT others(7): Show |
1 | a0001c0003t0002g0169 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.208+526_208+527ins others(14): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840422 | |||||||
| chr12:103840423 | T | C | 6 | a0001c0001t0010g0018 a0001c0004t0003g0020 a0001c0004t0003g0021 others(3): Show |
6 | HG02886.hp1 HG03516.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.208+526A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840423 | |||||||
| chr12:103840424 | C | T | 4 | a0001c0001t0010g0018 a0001c0004t0003g0020 a0001c0004t0003g0021 others(1): Show |
4 | HG02886.hp1 NA18952.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+525G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840424 | |||||||
| chr12:103840429 | C | T | 1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+520G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840429 | |||||||
| chr12:103840431 | A | C | 1 | a0001c0004t0017g0019 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.208+518T>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840431 | |||||||
| chr12:103840433 | T | C | 3 | a0001c0001t0010g0018 a0001c0005t0004g0353 a0001c0005t0004g0354 |
3 | HG02886.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.208+516A>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840433 | |||||||
| chr12:103840434 | C | T | 1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+515G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840434 | |||||||
| chr12:103840439 | C | T | 1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+510G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840439 | |||||||
| chr12:103840443 | C | CTCATCTC others(228): Show |
1 | a0001c0001t0010g0018 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208+505_208+506ins others(235): Show |
NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840443 | |||||||
| chr12:103840443 | C | T | 3 | a0001c0004t0003g0020 a0001c0004t0003g0021 a0001c0004t0017g0019 |
3 | NA18952.hp2 NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.208+506G>A | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840443 | |||||||
| chr12:103840682 | G | C | 18 | a0001c0001t0005g0370 a0001c0002t0001g0364 a0001c0002t0006g0357 others(15): Show |
18 | HG00733.hp2 HG01070.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.208+267C>G | NT5DC3 | ENSG00000111696.12 | transcript | ENST00000392876.8 | protein_coding | 1/13 | chr12 | 103840682 |