Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79684 |
| ensemblid | ENSG00000120458.13 |
| hgncid | 26266 |
| symbol | MSANTD2 |
| name | Myb/SANT DNA binding domain containing 2 |
| refseq_nuc | NM_001308027.2 |
| refseq_prot | NP_001294956.1 |
| ensembl_nuc | ENST00000374979.8 |
| ensembl_prot | ENSP00000364118.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 124766498 |
| end | 124800406 |
| strand | - |
| ver | v1.2 |
| region | chr11:124766498-124800406 |
| region5000 | chr11:124761498-124805406 |
| regionname0 | MSANTD2_chr11_124766498_124800406 |
| regionname5000 | MSANTD2_chr11_124761498_124805406 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 559 | 322 | 89 | 52 | 130 | 12 | 37 | 96 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | MAAPC others(554): Show |
chr11 | 124761498 | 124805406 |
| a0002 | 0/0 | 559 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | MAAPC others(554): Show |
chr11 | 124761498 | 124805406 |
| a0003 | 0/0 | 559 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | MAAPC others(554): Show |
chr11 | 124761498 | 124805406 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1677 | 312 | 86 | 50 | 129 | 10 | 35 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0001c0002 | 0/0 | 1677 | 6 | 0 | 2 | 0 | 2 | 2 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0001c0003 | 0/0 | 1677 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0001c0004 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0001c0007 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0002c0005 | 0/0 | 1677 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 | ||
| a0003c0006 | 0/0 | 1677 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | ATGGC others(1672): Show |
chr11 | 124761498 | 124805406 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2384 | 103 | 4 | 30 | 45 | 5 | 17 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2379): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0002 | 0/0 | 2386 | 79 | 35 | 6 | 34 | 0 | 4 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0003 | 0/0 | 2385 | 72 | 24 | 9 | 24 | 3 | 12 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2380): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0004 | 0/0 | 2386 | 39 | 23 | 2 | 14 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0005 | 0/0 | 2385 | 12 | 0 | 0 | 9 | 1 | 2 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2380): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0006 | 0/0 | 2385 | 4 | 0 | 3 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2380): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0007 | 0/0 | 2384 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2379): Show |
chr11 | 124761498 | 124805406 |
| a0001c0001t0008 | 0/0 | 2386 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0001c0002t0002 | 0/0 | 2386 | 5 | 0 | 1 | 0 | 2 | 2 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0001c0002t0003 | 0/0 | 2385 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2380): Show |
chr11 | 124761498 | 124805406 |
| a0001c0003t0002 | 0/0 | 2386 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0001c0004t0001 | 0/0 | 2384 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2379): Show |
chr11 | 124761498 | 124805406 |
| a0001c0007t0004 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| a0002c0005t0003 | 0/0 | 2385 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2380): Show |
chr11 | 124761498 | 124805406 |
| a0003c0006t0002 | 0/0 | 2386 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | GCGGT others(2381): Show |
chr11 | 124761498 | 124805406 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 2 | 7 | 1 | 3 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0002 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0004 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0001c0007t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0002c0005t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| a0003c0006t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0260 | EUR | GBR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | FIN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | FIN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0093 | EUR | FIN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00558 | hp1 | a0001 | c0004 | t0001 | g0036 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | CHS | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0262 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0151 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0261 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PUR | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0167 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0098 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | CDX | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | CDX | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02622 | hp1 | a0001 | c0007 | t0004 | g0199 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02735 | hp1 | a0002 | c0005 | t0003 | g0037 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0259 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0051 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03195 | hp1 | a0003 | c0006 | t0002 | g0237 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0149 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0177 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0080 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0190 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0112 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | CHB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18940 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18957 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0123 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | ASW | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ASW | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0187 | EUR | TSI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0150 | EUR | TSI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | TSI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0079 | AMR | CLM | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | USA | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | USA | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA18955 | hp2 | a0001 | c0001 | t0008 | g0144 | EAS | JPT | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | LWK | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0254 | REF | REF | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | MSANTD2_chr11_124761498_124805406 | MSANTD2 | chr11 | 124761498 | 124805406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:124767870 | C | T | 1 | a0003 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.986G>A | p.Arg329His | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 1012/2384 | 986/1680 | 329/559 | chr11 | 124767870 | |||
| chr11:124800251 | G | A | 1 | a0002 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.130C>T | p.Pro44Ser | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/4 | 156/2384 | 130/1680 | 44/559 | chr11 | 124800251 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:124767467 | T | C | 1 | a0001c0007 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1389A>G | p.Leu463Leu | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 1415/2384 | 1389/1680 | 463/559 | chr11 | 124767467 | |||
| chr11:124767713 | G | A | 1 | a0001c0003 | 2 | HG02145.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1143C>T | p.Ser381Ser | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 1169/2384 | 1143/1680 | 381/559 | chr11 | 124767713 | |||
| chr11:124800173 | G | A | 1 | a0001c0002 | 6 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(3): Show |
synonymous_variant | LOW | c.208C>T | p.Leu70Leu | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/4 | 234/2384 | 208/1680 | 70/559 | chr11 | 124800173 | |||
| chr11:124800252 | C | T | 1 | a0002c0005 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.129G>A | p.Thr43Thr | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/4 | 155/2384 | 129/1680 | 43/559 | chr11 | 124800252 | |||
| chr11:124800288 | C | T | 1 | a0001c0004 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.93G>A | p.Leu31Leu | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/4 | 119/2384 | 93/1680 | 31/559 | chr11 | 124800288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:124766515 | A | AT | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(1): Show |
78 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*660dupA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 660 | chr11 | 124766515 | ||||||
| chr11:124766515 | A | ATT | 2 | a0001c0001t0004 a0001c0007t0004 |
40 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*659_*660dupAA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 660 | chr11 | 124766515 | ||||||
| chr11:124766527 | T | TA | 1 | a0001c0001t0005 | 12 | HG00423.hp1 HG02027.hp1 HG02135.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*648dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 648 | chr11 | 124766527 | ||||||
| chr11:124766527 | T | TTA | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0002 others(2): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*648_*649insTA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 648 | chr11 | 124766527 | ||||||
| chr11:124766749 | G | A | 1 | a0001c0001t0006 | 4 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*427C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 427 | chr11 | 124766749 | ||||||
| chr11:124766957 | C | T | 1 | a0001c0001t0007 | 2 | NA18971.hp2 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*219G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 219 | chr11 | 124766957 | ||||||
| chr11:124767012 | T | C | 1 | a0001c0001t0008 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 164 | chr11 | 124767012 | ||||||
| chr11:124767013 | G | T | 1 | a0001c0001t0008 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 4/4 | 163 | chr11 | 124767013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:124768187 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.828-159C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768187 | |||||||
| chr11:124768241 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.828-213C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768241 | |||||||
| chr11:124768430 | T | C | 18 | a0001c0001t0001g0208 a0001c0001t0003g0015 a0001c0001t0003g0057 others(15): Show |
19 | HG01106.hp1 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.828-402A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768430 | |||||||
| chr11:124768873 | C | T | 11 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0031 others(8): Show |
16 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.828-845G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768873 | |||||||
| chr11:124768889 | T | C | 1 | a0001c0001t0003g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.828-861A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768889 | |||||||
| chr11:124768922 | T | C | 8 | a0001c0001t0003g0015 a0001c0001t0003g0085 a0001c0001t0003g0111 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.828-894A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124768922 | |||||||
| chr11:124769268 | A | G | 24 | a0001c0001t0003g0008 a0001c0001t0003g0013 a0001c0001t0003g0019 others(21): Show |
29 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.828-1240T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124769268 | |||||||
| chr11:124769358 | TGGCTATC others(4): Show |
T | 1 | a0001c0001t0002g0044 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.828-1341_828-1331d others(13): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124769358 | |||||||
| chr11:124770019 | T | C | 6 | a0001c0001t0003g0142 a0001c0001t0003g0244 a0001c0001t0004g0018 others(3): Show |
7 | NA18947.hp1 NA18973.hp1 NA18979.hp1 others(4): Show |
intron_variant | MODIFIER | c.828-1991A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770019 | |||||||
| chr11:124770306 | G | T | 1 | a0001c0001t0002g0113 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.828-2278C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770306 | |||||||
| chr11:124770314 | GTT | G | 112 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(109): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.828-2288_828-2287d others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770314 | |||||||
| chr11:124770314 | GTTT | G | 17 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.828-2289_828-2287d others(5): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770314 | |||||||
| chr11:124770315 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.828-2287A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770315 | |||||||
| chr11:124770320 | T | G | 20 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0140 others(17): Show |
25 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.828-2292A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770320 | |||||||
| chr11:124770375 | T | C | 110 | a0001c0001t0001g0208 a0001c0001t0002g0003 a0001c0001t0002g0007 others(107): Show |
132 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.828-2347A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770375 | |||||||
| chr11:124770473 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0252 |
2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.828-2445T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770473 | |||||||
| chr11:124770554 | C | T | 1 | a0001c0002t0002g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.827+2440G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770554 | |||||||
| chr11:124770743 | T | C | 2 | a0001c0001t0003g0201 a0001c0001t0003g0226 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.827+2251A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770743 | |||||||
| chr11:124770773 | T | C | 112 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(109): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.827+2221A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770773 | |||||||
| chr11:124770780 | G | GT | 86 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0058 others(83): Show |
99 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.827+2213dupA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770780 | |||||||
| chr11:124770780 | G | GTT | 22 | a0001c0001t0002g0003 a0001c0001t0002g0027 a0001c0001t0002g0028 others(19): Show |
28 | HG01109.hp2 HG01884.hp1 HG02129.hp1 others(25): Show |
intron_variant | MODIFIER | c.827+2212_827+2213d others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770780 | |||||||
| chr11:124770780 | GT | G | 7 | a0001c0001t0002g0107 a0001c0001t0004g0165 a0001c0001t0004g0179 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.827+2213delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770780 | |||||||
| chr11:124770780 | GTT | G | 11 | a0001c0001t0004g0024 a0001c0001t0004g0034 a0001c0001t0004g0050 others(8): Show |
13 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.827+2212_827+2213d others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770780 | |||||||
| chr11:124770968 | G | A | 5 | a0001c0001t0002g0116 a0001c0001t0002g0145 a0001c0002t0002g0035 others(2): Show |
6 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.827+2026C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124770968 | |||||||
| chr11:124771264 | C | T | 1 | a0001c0001t0003g0067 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.827+1730G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124771264 | |||||||
| chr11:124771523 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.827+1471T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124771523 | |||||||
| chr11:124771830 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.827+1164T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124771830 | |||||||
| chr11:124771954 | C | T | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.827+1040G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124771954 | |||||||
| chr11:124772056 | G | A | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.827+938C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772056 | |||||||
| chr11:124772087 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.827+907G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772087 | |||||||
| chr11:124772411 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+583G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772411 | |||||||
| chr11:124772412 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+582T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772412 | |||||||
| chr11:124772421 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+573C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772421 | |||||||
| chr11:124772423 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+571A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772423 | |||||||
| chr11:124772428 | T | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+566A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772428 | |||||||
| chr11:124772430 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+564T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772430 | |||||||
| chr11:124772431 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+563C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772431 | |||||||
| chr11:124772432 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+562T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772432 | |||||||
| chr11:124772434 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+560T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772434 | |||||||
| chr11:124772435 | C | CCGCCTTG others(8): Show |
1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+558_827+559ins others(15): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772435 | |||||||
| chr11:124772437 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+557T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772437 | |||||||
| chr11:124772439 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+555T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772439 | |||||||
| chr11:124772441 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+553T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772441 | |||||||
| chr11:124772442 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+552T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772442 | |||||||
| chr11:124772443 | C | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+551G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772443 | |||||||
| chr11:124772447 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+547A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772447 | |||||||
| chr11:124772454 | C | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+540G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772454 | |||||||
| chr11:124772455 | T | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+539A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772455 | |||||||
| chr11:124772457 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+537C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772457 | |||||||
| chr11:124772459 | T | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+535A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772459 | |||||||
| chr11:124772460 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+534C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772460 | |||||||
| chr11:124772461 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+533C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772461 | |||||||
| chr11:124772463 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+531A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772463 | |||||||
| chr11:124772466 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+528C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772466 | |||||||
| chr11:124772467 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+527C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772467 | |||||||
| chr11:124772470 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+524C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772470 | |||||||
| chr11:124772485 | C | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+509G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772485 | |||||||
| chr11:124772486 | C | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+508G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772486 | |||||||
| chr11:124772489 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+505C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772489 | |||||||
| chr11:124772496 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+498C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772496 | |||||||
| chr11:124772497 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+497C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772497 | |||||||
| chr11:124772501 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+493C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772501 | |||||||
| chr11:124772503 | T | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+491A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772503 | |||||||
| chr11:124772507 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+487C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772507 | |||||||
| chr11:124772509 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+485C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772509 | |||||||
| chr11:124772510 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+484C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772510 | |||||||
| chr11:124772511 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+483C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772511 | |||||||
| chr11:124772513 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+481C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772513 | |||||||
| chr11:124772515 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+479T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772515 | |||||||
| chr11:124772517 | C | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+477G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772517 | |||||||
| chr11:124772518 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+476T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772518 | |||||||
| chr11:124772526 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+468T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772526 | |||||||
| chr11:124772532 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+462A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772532 | |||||||
| chr11:124772533 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0002g0222 |
3 | HG00738.hp1 HG01192.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.827+461G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772533 | |||||||
| chr11:124772535 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+459T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772535 | |||||||
| chr11:124772536 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+458C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772536 | |||||||
| chr11:124772538 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+456A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772538 | |||||||
| chr11:124772539 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+455T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772539 | |||||||
| chr11:124772543 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+451G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772543 | |||||||
| chr11:124772544 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+450A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772544 | |||||||
| chr11:124772549 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+445T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772549 | |||||||
| chr11:124772558 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+436T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772558 | |||||||
| chr11:124772567 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+427G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772567 | |||||||
| chr11:124772569 | C | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+425G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772569 | |||||||
| chr11:124772570 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+424A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772570 | |||||||
| chr11:124772571 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+423T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772571 | |||||||
| chr11:124772572 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+422G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772572 | |||||||
| chr11:124772574 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+420T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772574 | |||||||
| chr11:124772575 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+419T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772575 | |||||||
| chr11:124772576 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+418T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772576 | |||||||
| chr11:124772577 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+417A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772577 | |||||||
| chr11:124772580 | A | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+414T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772580 | |||||||
| chr11:124772584 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+410T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772584 | |||||||
| chr11:124772585 | A | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+409T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772585 | |||||||
| chr11:124772598 | G | A | 2 | a0001c0001t0003g0201 a0001c0001t0003g0226 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.827+396C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772598 | |||||||
| chr11:124772598 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+396C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772598 | |||||||
| chr11:124772602 | T | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+392A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772602 | |||||||
| chr11:124772603 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+391C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772603 | |||||||
| chr11:124772604 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+390C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772604 | |||||||
| chr11:124772606 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+388C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772606 | |||||||
| chr11:124772608 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+386C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772608 | |||||||
| chr11:124772610 | G | T | 1 | a0001c0001t0002g0222 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.827+384C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772610 | |||||||
| chr11:124772704 | A | T | 128 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(125): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.827+290T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772704 | |||||||
| chr11:124772732 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.827+262C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772732 | |||||||
| chr11:124772742 | C | CA | 42 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0039 others(39): Show |
45 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.827+251dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAA | C | 16 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0031 others(13): Show |
22 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.827+249_827+251del others(3): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAAA | C | 10 | a0001c0001t0001g0208 a0001c0001t0003g0057 a0001c0001t0003g0079 others(7): Show |
10 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.827+248_827+251del others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAAAA | C | 20 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0003g0142 others(17): Show |
25 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.827+247_827+251del others(5): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAAAAAA others(2): Show |
C | 55 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0014 others(52): Show |
65 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.827+243_827+251del others(9): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0088 a0001c0001t0002g0243 |
4 | HG02896.hp2 NA18971.hp1 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.827+242_827+251del others(10): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772742 | CAAAAAAA others(5): Show |
C | 17 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.827+240_827+251del others(12): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772742 | |||||||
| chr11:124772775 | G | A | 1 | a0001c0001t0003g0073 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.827+219C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772775 | |||||||
| chr11:124772778 | T | C | 22 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0140 others(19): Show |
27 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.827+216A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772778 | |||||||
| chr11:124772811 | C | T | 2 | a0001c0001t0003g0055 a0001c0001t0003g0056 |
2 | HG02293.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.827+183G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 3/3 | chr11 | 124772811 | |||||||
| chr11:124773093 | A | G | 17 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.767-39T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124773093 | |||||||
| chr11:124773143 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0215 a0001c0001t0001g0227 |
3 | NA18986.hp1 NA18989.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.767-89G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124773143 | |||||||
| chr11:124773603 | C | T | 1 | a0001c0001t0004g0236 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.767-549G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124773603 | |||||||
| chr11:124773797 | G | A | 72 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0010 others(69): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.767-743C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124773797 | |||||||
| chr11:124773940 | C | T | 129 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(126): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.766+779G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124773940 | |||||||
| chr11:124774043 | A | C | 112 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(109): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.766+676T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774043 | |||||||
| chr11:124774066 | G | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0191 a0001c0001t0001g0194 |
3 | HG02080.hp1 NA18973.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.766+653C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774066 | |||||||
| chr11:124774079 | C | A | 17 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(14): Show |
20 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.766+640G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774079 | |||||||
| chr11:124774331 | A | AGTCAT | 129 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(126): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.766+387_766+388ins others(5): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774331 | |||||||
| chr11:124774494 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0118 |
3 | HG01081.hp2 HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.766+225G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774494 | |||||||
| chr11:124774613 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.766+106A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774613 | |||||||
| chr11:124774630 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.766+89C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 2/3 | chr11 | 124774630 | |||||||
| chr11:124775398 | A | G | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.511-424T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124775398 | |||||||
| chr11:124775429 | CT | C | 70 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0010 others(67): Show |
86 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.511-456delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124775429 | |||||||
| chr11:124775638 | G | A | 2 | a0001c0001t0003g0057 a0001c0001t0003g0174 |
2 | HG01106.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.511-664C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124775638 | |||||||
| chr11:124775775 | T | C | 1 | a0001c0001t0003g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.511-801A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124775775 | |||||||
| chr11:124776036 | GT | G | 19 | a0001c0001t0001g0208 a0001c0001t0003g0015 a0001c0001t0003g0057 others(16): Show |
20 | HG00642.hp2 HG01106.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.511-1063delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776036 | |||||||
| chr11:124776201 | G | C | 4 | a0001c0001t0004g0033 a0001c0001t0004g0034 a0001c0001t0004g0050 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-1227C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776201 | |||||||
| chr11:124776255 | A | G | 1 | a0001c0001t0004g0192 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.511-1281T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776255 | |||||||
| chr11:124776267 | A | C | 131 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(128): Show |
156 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.511-1293T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776267 | |||||||
| chr11:124776291 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.511-1317G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776291 | |||||||
| chr11:124776329 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0173 |
2 | HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.511-1355C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776329 | |||||||
| chr11:124776446 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.511-1472G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776446 | |||||||
| chr11:124776524 | C | T | 1 | a0001c0001t0003g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.511-1550G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776524 | |||||||
| chr11:124776726 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0118 |
3 | HG01081.hp2 HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.511-1752A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776726 | |||||||
| chr11:124776913 | C | T | 1 | a0001c0001t0006g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.511-1939G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124776913 | |||||||
| chr11:124777030 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.511-2056G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124777030 | |||||||
| chr11:124777096 | A | G | 2 | a0001c0001t0003g0049 a0001c0001t0003g0068 |
2 | HG02155.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.511-2122T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124777096 | |||||||
| chr11:124777331 | G | T | 12 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(9): Show |
15 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-2357C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124777331 | |||||||
| chr11:124777368 | G | A | 7 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0004g0091 others(4): Show |
7 | HG01109.hp1 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-2394C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124777368 | |||||||
| chr11:124777902 | GA | G | 128 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(125): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.511-2929delT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124777902 | |||||||
| chr11:124778014 | C | T | 1 | a0001c0001t0003g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511-3040G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778014 | |||||||
| chr11:124778038 | G | A | 32 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0026 others(29): Show |
38 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.511-3064C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778038 | |||||||
| chr11:124778242 | T | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0029 a0001c0001t0002g0100 others(1): Show |
6 | HG02280.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-3268A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778242 | |||||||
| chr11:124778471 | T | G | 32 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0026 others(29): Show |
38 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.511-3497A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778471 | |||||||
| chr11:124778579 | T | C | 2 | a0001c0001t0002g0217 a0001c0001t0002g0230 |
2 | NA18991.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.511-3605A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778579 | |||||||
| chr11:124778591 | C | T | 51 | a0001c0001t0002g0007 a0001c0001t0002g0010 a0001c0001t0002g0012 others(48): Show |
61 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.511-3617G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778591 | |||||||
| chr11:124778692 | C | T | 1 | a0001c0001t0003g0065 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.511-3718G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778692 | |||||||
| chr11:124778785 | T | A | 2 | a0001c0003t0002g0098 a0001c0003t0002g0149 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.511-3811A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778785 | |||||||
| chr11:124778962 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0118 |
3 | HG01081.hp2 HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.511-3988A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778962 | |||||||
| chr11:124778966 | C | T | 3 | a0001c0001t0003g0054 a0001c0001t0003g0062 a0001c0001t0003g0063 |
3 | HG02615.hp1 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.511-3992G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124778966 | |||||||
| chr11:124779032 | T | G | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.511-4058A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124779032 | |||||||
| chr11:124779631 | A | G | 1 | a0001c0001t0003g0160 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.511-4657T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124779631 | |||||||
| chr11:124779640 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0148 |
2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.511-4666C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124779640 | |||||||
| chr11:124780220 | C | A | 1 | a0001c0001t0004g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.511-5246G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780220 | |||||||
| chr11:124780230 | C | A | 1 | a0001c0001t0003g0084 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-5256G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780230 | |||||||
| chr11:124780268 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.511-5294G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780268 | |||||||
| chr11:124780326 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.511-5352T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780326 | |||||||
| chr11:124780588 | G | A | 128 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(125): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.511-5614C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780588 | |||||||
| chr11:124780611 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-5637G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780611 | |||||||
| chr11:124780957 | C | T | 17 | a0001c0001t0001g0208 a0001c0001t0003g0015 a0001c0001t0003g0057 others(14): Show |
18 | HG01106.hp1 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.511-5983G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124780957 | |||||||
| chr11:124781047 | G | A | 1 | a0001c0001t0004g0253 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.511-6073C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781047 | |||||||
| chr11:124781138 | G | A | 11 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0031 others(8): Show |
16 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-6164C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781138 | |||||||
| chr11:124781183 | C | CA | 21 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0137 others(18): Show |
21 | HG00438.hp1 HG01243.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.511-6210dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781183 | |||||||
| chr11:124781183 | CA | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0031 others(9): Show |
17 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-6210delT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781183 | |||||||
| chr11:124781201 | A | T | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.511-6227T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781201 | |||||||
| chr11:124781239 | A | AAAATATA others(154): Show |
1 | a0001c0001t0004g0181 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.511-6426_511-6266d others(163): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781239 | |||||||
| chr11:124781317 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01106.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.511-6343C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781317 | |||||||
| chr11:124781374 | ATTAAC | A | 8 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0004g0091 others(5): Show |
8 | HG01109.hp1 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-6405_511-6401d others(7): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781374 | |||||||
| chr11:124781393 | T | C | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.511-6419A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781393 | |||||||
| chr11:124781584 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6610A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781584 | |||||||
| chr11:124781595 | G | GACTCAAC others(3): Show |
1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6622_511-6621i others(12): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781595 | |||||||
| chr11:124781627 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6653G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781627 | |||||||
| chr11:124781631 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6657A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781631 | |||||||
| chr11:124781633 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6659G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781633 | |||||||
| chr11:124781638 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6664C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781638 | |||||||
| chr11:124781641 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6667T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781641 | |||||||
| chr11:124781642 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.511-6668A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781642 | |||||||
| chr11:124781647 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6673T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781647 | |||||||
| chr11:124781650 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6676C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781650 | |||||||
| chr11:124781651 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6677A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781651 | |||||||
| chr11:124781652 | C | CT | 8 | a0001c0001t0001g0066 a0001c0001t0001g0104 a0001c0001t0001g0128 others(5): Show |
8 | HG01071.hp2 HG01175.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-6679dupA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781652 | |||||||
| chr11:124781652 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6678G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781652 | |||||||
| chr11:124781652 | CT | C | 40 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0026 others(37): Show |
48 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.511-6679delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781652 | |||||||
| chr11:124781652 | CTT | C | 82 | a0001c0001t0001g0208 a0001c0001t0002g0003 a0001c0001t0002g0007 others(79): Show |
98 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.511-6680_511-6679d others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781652 | |||||||
| chr11:124781663 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6689A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781663 | |||||||
| chr11:124781665 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6691A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781665 | |||||||
| chr11:124781667 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6693A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781667 | |||||||
| chr11:124781670 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6696A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781670 | |||||||
| chr11:124781672 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6698T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781672 | |||||||
| chr11:124781673 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6699C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781673 | |||||||
| chr11:124781678 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6704T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781678 | |||||||
| chr11:124781679 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6705A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781679 | |||||||
| chr11:124781679 | T | G | 115 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(112): Show |
137 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.511-6705A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781679 | |||||||
| chr11:124781680 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6706A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781680 | |||||||
| chr11:124781681 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6707G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781681 | |||||||
| chr11:124781686 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6712A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781686 | |||||||
| chr11:124781689 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6715C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781689 | |||||||
| chr11:124781690 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6716A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781690 | |||||||
| chr11:124781691 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6717G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781691 | |||||||
| chr11:124781694 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6720G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781694 | |||||||
| chr11:124781695 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6721A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781695 | |||||||
| chr11:124781696 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6722T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781696 | |||||||
| chr11:124781712 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6738C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781712 | |||||||
| chr11:124781713 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6739G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781713 | |||||||
| chr11:124781723 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6749C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781723 | |||||||
| chr11:124781736 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6762A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781736 | |||||||
| chr11:124781738 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6764A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781738 | |||||||
| chr11:124781739 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6765C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781739 | |||||||
| chr11:124781747 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6773C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781747 | |||||||
| chr11:124781754 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6780C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781754 | |||||||
| chr11:124781755 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6781A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781755 | |||||||
| chr11:124781756 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6782C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781756 | |||||||
| chr11:124781759 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6785A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781759 | |||||||
| chr11:124781764 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6790A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781764 | |||||||
| chr11:124781765 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6791C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781765 | |||||||
| chr11:124781766 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6792G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781766 | |||||||
| chr11:124781778 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.511-6804C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781778 | |||||||
| chr11:124781839 | GACGGGGT others(3): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6875_511-6866d others(12): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781839 | |||||||
| chr11:124781906 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.511-6932C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781906 | |||||||
| chr11:124781932 | C | T | 2 | a0001c0001t0007g0123 a0001c0001t0007g0124 |
2 | NA18971.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.511-6958G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124781932 | |||||||
| chr11:124782170 | A | G | 116 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(113): Show |
138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.511-7196T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124782170 | |||||||
| chr11:124782226 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.511-7252G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124782226 | |||||||
| chr11:124782285 | T | TA | 118 | a0001c0001t0001g0064 a0001c0001t0001g0139 a0001c0001t0001g0166 others(115): Show |
140 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.511-7312dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124782285 | |||||||
| chr11:124782452 | C | A | 1 | a0001c0001t0002g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.511-7478G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124782452 | |||||||
| chr11:124782893 | G | A | 12 | a0001c0001t0004g0024 a0001c0001t0004g0033 a0001c0001t0004g0034 others(9): Show |
15 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-7919C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124782893 | |||||||
| chr11:124783423 | C | G | 33 | a0001c0001t0001g0166 a0001c0001t0001g0252 a0001c0001t0002g0026 others(30): Show |
39 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.511-8449G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124783423 | |||||||
| chr11:124784030 | G | C | 124 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0252 others(121): Show |
149 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.511-9056C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784030 | |||||||
| chr11:124784120 | A | G | 7 | a0001c0001t0004g0024 a0001c0001t0004g0051 a0001c0001t0004g0052 others(4): Show |
8 | HG02055.hp2 HG02258.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-9146T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784120 | |||||||
| chr11:124784157 | G | GA | 8 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0044 others(5): Show |
11 | HG00408.hp2 HG02129.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-9184dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784157 | |||||||
| chr11:124784329 | A | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0029 a0001c0001t0002g0232 |
5 | HG02280.hp2 HG02630.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-9355T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784329 | |||||||
| chr11:124784442 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.511-9468G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784442 | |||||||
| chr11:124784452 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0172 |
2 | NA18992.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.511-9478T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784452 | |||||||
| chr11:124784453 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0172 |
2 | NA18992.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.511-9479A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784453 | |||||||
| chr11:124784482 | AC | A | 14 | a0001c0001t0001g0041 a0001c0001t0001g0208 a0001c0001t0001g0250 others(11): Show |
14 | HG01123.hp2 HG01169.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-9509delG | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784482 | |||||||
| chr11:124784482 | ACC | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(212): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.511-9510_511-9509d others(4): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784482 | |||||||
| chr11:124784486 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.511-9512G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784486 | |||||||
| chr11:124784489 | C | G | 1 | a0001c0003t0002g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.511-9515G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784489 | |||||||
| chr11:124784590 | G | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0031 others(13): Show |
21 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.511-9616C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784590 | |||||||
| chr11:124784608 | C | G | 3 | a0001c0001t0002g0088 a0001c0001t0004g0081 a0001c0001t0004g0082 |
3 | HG02257.hp1 HG02486.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.511-9634G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784608 | |||||||
| chr11:124784653 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.511-9679G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784653 | |||||||
| chr11:124784962 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.511-9988A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124784962 | |||||||
| chr11:124785083 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.511-10109T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785083 | |||||||
| chr11:124785151 | G | C | 1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.511-10177C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785151 | |||||||
| chr11:124785239 | G | T | 5 | a0001c0001t0003g0079 a0001c0001t0004g0050 a0001c0001t0004g0051 others(2): Show |
5 | HG01123.hp2 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-10265C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785239 | |||||||
| chr11:124785259 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.511-10285G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785259 | |||||||
| chr11:124785436 | C | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.511-10462G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785436 | |||||||
| chr11:124785457 | T | C | 1 | a0001c0002t0002g0259 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.511-10483A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785457 | |||||||
| chr11:124785475 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.511-10501G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785475 | |||||||
| chr11:124785484 | C | A | 67 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(64): Show |
77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.511-10510G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785484 | |||||||
| chr11:124785525 | G | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
9 | HG02280.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-10551C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785525 | |||||||
| chr11:124785591 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0003g0112 a0001c0001t0003g0162 |
3 | HG03017.hp1 HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.511-10617C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785591 | |||||||
| chr11:124785695 | G | T | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.511-10721C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785695 | |||||||
| chr11:124785708 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.511-10734C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785708 | |||||||
| chr11:124785732 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0003g0022 |
3 | HG00642.hp1 HG01081.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.511-10758C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785732 | |||||||
| chr11:124785745 | T | TATATATA others(31): Show |
1 | a0001c0001t0003g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511-10809_511-1077 others(42): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785745 | |||||||
| chr11:124785855 | C | T | 148 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(145): Show |
175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.511-10881G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124785855 | |||||||
| chr11:124786095 | C | CT | 18 | a0001c0001t0001g0120 a0001c0001t0001g0166 a0001c0001t0002g0026 others(15): Show |
19 | HG01123.hp2 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.511-11122dupA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786095 | |||||||
| chr11:124786095 | CT | C | 85 | a0001c0001t0001g0021 a0001c0001t0001g0058 a0001c0001t0001g0064 others(82): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.511-11122delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786095 | |||||||
| chr11:124786095 | CTT | C | 7 | a0001c0001t0002g0014 a0001c0001t0002g0028 a0001c0001t0002g0029 others(4): Show |
10 | HG01169.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-11123_511-1112 others(6): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786095 | |||||||
| chr11:124786095 | CTTT | C | 6 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(3): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-11124_511-1112 others(7): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786095 | |||||||
| chr11:124786095 | CTTTTTTT | C | 34 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
41 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.511-11128_511-1112 others(11): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786095 | |||||||
| chr11:124786098 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.511-11124A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786098 | |||||||
| chr11:124786223 | G | A | 1 | a0001c0001t0003g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.511-11249C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786223 | |||||||
| chr11:124786231 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.511-11257G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786231 | |||||||
| chr11:124786232 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0210 |
3 | HG01106.hp2 HG01123.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.511-11258C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786232 | |||||||
| chr11:124786263 | C | T | 6 | a0001c0001t0002g0031 a0001c0001t0002g0239 a0001c0001t0003g0238 others(3): Show |
7 | HG01109.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.511-11289G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786263 | |||||||
| chr11:124786814 | G | A | 4 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-11840C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786814 | |||||||
| chr11:124786840 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.511-11866G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124786840 | |||||||
| chr11:124787244 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.511-12270G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787244 | |||||||
| chr11:124787259 | T | C | 38 | a0001c0001t0001g0119 a0001c0001t0001g0185 a0001c0001t0001g0188 others(35): Show |
46 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.511-12285A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787259 | |||||||
| chr11:124787287 | T | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(68): Show |
81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.511-12313A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787287 | |||||||
| chr11:124787306 | C | G | 6 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(3): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-12332G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787306 | |||||||
| chr11:124787366 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.511-12392G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787366 | |||||||
| chr11:124787367 | G | A | 11 | a0001c0001t0001g0166 a0001c0001t0002g0106 a0001c0001t0002g0107 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-12393C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787367 | |||||||
| chr11:124787455 | A | G | 71 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(68): Show |
81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.510+12416T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787455 | |||||||
| chr11:124787561 | A | G | 6 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(3): Show |
6 | HG02572.hp2 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+12310T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787561 | |||||||
| chr11:124787700 | A | G | 34 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
41 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+12171T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787700 | |||||||
| chr11:124787769 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510+12102A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787769 | |||||||
| chr11:124787883 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0108 |
3 | HG00140.hp2 HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.510+11988T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124787883 | |||||||
| chr11:124788081 | C | CA | 18 | a0001c0001t0001g0159 a0001c0001t0001g0208 a0001c0001t0002g0077 others(15): Show |
20 | HG00738.hp2 HG01261.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+11789dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788081 | |||||||
| chr11:124788081 | C | CAA | 43 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(40): Show |
51 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.510+11788_510+1178 others(6): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788081 | |||||||
| chr11:124788121 | A | G | 1 | a0001c0001t0004g0165 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.510+11750T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788121 | |||||||
| chr11:124788262 | G | A | 6 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(3): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+11609C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788262 | |||||||
| chr11:124788343 | G | A | 70 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(67): Show |
80 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.510+11528C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788343 | |||||||
| chr11:124788441 | T | C | 65 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(62): Show |
75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.510+11430A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788441 | |||||||
| chr11:124788504 | T | C | 1 | a0001c0001t0003g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.510+11367A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788504 | |||||||
| chr11:124788811 | A | G | 3 | a0001c0001t0002g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG00544.hp1 HG02074.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.510+11060T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788811 | |||||||
| chr11:124788812 | T | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0090 a0001c0001t0001g0094 others(17): Show |
25 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.510+11059A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788812 | |||||||
| chr11:124788823 | A | G | 64 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(61): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.510+11048T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788823 | |||||||
| chr11:124788995 | G | A | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510+10876C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124788995 | |||||||
| chr11:124789072 | C | T | 64 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(61): Show |
74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.510+10799G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789072 | |||||||
| chr11:124789163 | C | T | 2 | a0001c0001t0004g0050 a0001c0001t0004g0051 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510+10708G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789163 | |||||||
| chr11:124789479 | A | G | 6 | a0001c0001t0002g0202 a0001c0001t0003g0203 a0001c0001t0003g0204 others(3): Show |
6 | HG02723.hp2 HG02886.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+10392T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789479 | |||||||
| chr11:124789600 | G | T | 1 | a0001c0001t0001g0058 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.510+10271C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789600 | |||||||
| chr11:124789605 | G | A | 12 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
14 | HG00423.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+10266C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789605 | |||||||
| chr11:124789720 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.510+10151A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789720 | |||||||
| chr11:124789755 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510+10116G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789755 | |||||||
| chr11:124789790 | C | G | 2 | a0001c0001t0004g0081 a0001c0001t0004g0082 |
2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.510+10081G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789790 | |||||||
| chr11:124789812 | A | G | 24 | a0001c0001t0001g0215 a0001c0001t0001g0221 a0001c0001t0001g0227 others(21): Show |
27 | HG01071.hp1 HG02559.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+10059T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789812 | |||||||
| chr11:124789906 | A | T | 1 | a0001c0001t0002g0231 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+9965T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789906 | |||||||
| chr11:124789950 | C | T | 4 | a0001c0001t0002g0031 a0001c0001t0002g0239 a0001c0001t0003g0238 others(1): Show |
5 | HG02886.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+9921G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124789950 | |||||||
| chr11:124790288 | A | C | 119 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(116): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.510+9583T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790288 | |||||||
| chr11:124790315 | G | T | 18 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0002g0184 others(15): Show |
20 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+9556C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790315 | |||||||
| chr11:124790554 | G | A | 18 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0002g0184 others(15): Show |
20 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+9317C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790554 | |||||||
| chr11:124790560 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.510+9311T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790560 | |||||||
| chr11:124790724 | T | C | 4 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+9147A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790724 | |||||||
| chr11:124790755 | C | A | 18 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0002g0184 others(15): Show |
20 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+9116G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790755 | |||||||
| chr11:124790888 | G | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0107 |
2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.510+8983C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790888 | |||||||
| chr11:124790960 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.510+8911T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790960 | |||||||
| chr11:124790989 | T | G | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8882A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790989 | |||||||
| chr11:124790990 | A | G | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8881T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790990 | |||||||
| chr11:124790995 | T | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8876A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790995 | |||||||
| chr11:124790998 | G | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8873C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124790998 | |||||||
| chr11:124791000 | T | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8871A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791000 | |||||||
| chr11:124791004 | G | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8867C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791004 | |||||||
| chr11:124791005 | C | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8866G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791005 | |||||||
| chr11:124791006 | C | CAAGATTT others(4): Show |
1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8864_510+8865i others(13): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791006 | |||||||
| chr11:124791012 | G | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8859C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791012 | |||||||
| chr11:124791015 | G | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8856C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791015 | |||||||
| chr11:124791023 | A | C | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8848T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791023 | |||||||
| chr11:124791041 | G | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8830C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791041 | |||||||
| chr11:124791059 | A | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8812T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791059 | |||||||
| chr11:124791061 | A | C | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8810T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791061 | |||||||
| chr11:124791066 | G | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8805C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791066 | |||||||
| chr11:124791069 | G | C | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8802C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791069 | |||||||
| chr11:124791072 | G | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8799C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791072 | |||||||
| chr11:124791076 | A | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8795T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791076 | |||||||
| chr11:124791077 | G | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8794C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791077 | |||||||
| chr11:124791078 | A | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8793T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791078 | |||||||
| chr11:124791079 | T | G | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8792A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791079 | |||||||
| chr11:124791083 | G | A | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8788C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791083 | |||||||
| chr11:124791085 | G | C | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8786C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791085 | |||||||
| chr11:124791092 | A | T | 1 | a0001c0001t0005g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510+8779T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791092 | |||||||
| chr11:124791142 | G | A | 24 | a0001c0001t0001g0215 a0001c0001t0001g0221 a0001c0001t0001g0227 others(21): Show |
27 | HG01071.hp1 HG02559.hp1 HG02559.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+8729C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791142 | |||||||
| chr11:124791188 | T | C | 6 | a0001c0001t0002g0014 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
9 | HG02280.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+8683A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791188 | |||||||
| chr11:124791218 | C | A | 2 | a0001c0001t0003g0160 a0001c0001t0003g0161 |
2 | NA18943.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.510+8653G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791218 | |||||||
| chr11:124791370 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0038 |
3 | NA18962.hp1 NA18978.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.510+8501C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791370 | |||||||
| chr11:124791380 | C | G | 18 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0002g0184 others(15): Show |
20 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+8491G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791380 | |||||||
| chr11:124791442 | G | T | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.510+8429C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791442 | |||||||
| chr11:124791475 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510+8396C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791475 | |||||||
| chr11:124791599 | T | A | 6 | a0001c0001t0002g0014 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
9 | HG02280.hp2 HG02630.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+8272A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791599 | |||||||
| chr11:124791673 | C | T | 4 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0003g0256 others(1): Show |
4 | HG00140.hp1 HG00323.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+8198G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791673 | |||||||
| chr11:124791780 | T | A | 1 | a0001c0001t0002g0044 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.510+8091A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791780 | |||||||
| chr11:124791802 | C | T | 18 | a0001c0001t0001g0208 a0001c0001t0001g0252 a0001c0001t0002g0184 others(15): Show |
20 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+8069G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124791802 | |||||||
| chr11:124792010 | A | G | 34 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
41 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+7861T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792010 | |||||||
| chr11:124792060 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+7811T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792060 | |||||||
| chr11:124792330 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.510+7541C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792330 | |||||||
| chr11:124792330 | G | T | 5 | a0001c0001t0003g0079 a0001c0001t0004g0050 a0001c0001t0004g0051 others(2): Show |
5 | HG01123.hp2 HG02647.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+7541C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792330 | |||||||
| chr11:124792455 | G | T | 2 | a0001c0001t0001g0105 a0001c0001t0003g0162 |
2 | HG03017.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.510+7416C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792455 | |||||||
| chr11:124792582 | T | C | 1 | a0001c0001t0004g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.510+7289A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792582 | |||||||
| chr11:124792751 | C | G | 1 | a0001c0001t0003g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+7120G>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792751 | |||||||
| chr11:124792878 | C | A | 1 | a0001c0001t0002g0232 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.510+6993G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792878 | |||||||
| chr11:124792983 | C | T | 1 | a0001c0001t0003g0056 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.510+6888G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124792983 | |||||||
| chr11:124793345 | T | C | 1 | a0001c0001t0005g0190 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.510+6526A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793345 | |||||||
| chr11:124793551 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510+6320T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793551 | |||||||
| chr11:124793796 | A | AT | 37 | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0001g0108 others(34): Show |
41 | HG00140.hp2 HG01071.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+6074dupA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793796 | |||||||
| chr11:124793796 | AT | A | 65 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(62): Show |
76 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.510+6074delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793796 | |||||||
| chr11:124793821 | A | G | 70 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(67): Show |
81 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.510+6050T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793821 | |||||||
| chr11:124793896 | T | G | 4 | a0001c0001t0002g0031 a0001c0001t0002g0239 a0001c0001t0003g0238 others(1): Show |
5 | HG02886.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+5975A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793896 | |||||||
| chr11:124793914 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0169 |
3 | HG00621.hp1 HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.510+5957A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124793914 | |||||||
| chr11:124794195 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.510+5676A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794195 | |||||||
| chr11:124794238 | CT | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0045 |
4 | HG00408.hp2 HG02129.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+5632delA | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794238 | |||||||
| chr11:124794249 | A | T | 35 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(32): Show |
42 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.510+5622T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794249 | |||||||
| chr11:124794401 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.510+5470G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794401 | |||||||
| chr11:124794569 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510+5302A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794569 | |||||||
| chr11:124794824 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510+5047A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794824 | |||||||
| chr11:124794889 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.510+4982A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124794889 | |||||||
| chr11:124795124 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.510+4747G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795124 | |||||||
| chr11:124795148 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.510+4723G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795148 | |||||||
| chr11:124795243 | T | G | 34 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
41 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+4628A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795243 | |||||||
| chr11:124795280 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.510+4591G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795280 | |||||||
| chr11:124795297 | A | G | 12 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
14 | HG00423.hp1 HG01106.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+4574T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795297 | |||||||
| chr11:124795326 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.510+4545G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795326 | |||||||
| chr11:124795462 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.510+4409A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795462 | |||||||
| chr11:124795564 | A | AC | 4 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0003g0103 others(1): Show |
4 | HG02027.hp1 HG03516.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+4306dupG | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795564 | |||||||
| chr11:124795638 | T | C | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510+4233A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795638 | |||||||
| chr11:124795707 | A | G | 34 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(31): Show |
41 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+4164T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795707 | |||||||
| chr11:124795718 | A | G | 66 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(63): Show |
77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.510+4153T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795718 | |||||||
| chr11:124795885 | T | C | 66 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(63): Show |
77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.510+3986A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795885 | |||||||
| chr11:124795940 | C | T | 5 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0231 others(2): Show |
7 | HG02280.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+3931G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124795940 | |||||||
| chr11:124796035 | A | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0089 a0001c0001t0004g0102 others(2): Show |
6 | NA18940.hp1 NA18947.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+3836T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796035 | |||||||
| chr11:124796170 | C | T | 66 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(63): Show |
77 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.510+3701G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796170 | |||||||
| chr11:124796185 | T | C | 153 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(150): Show |
181 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.510+3686A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796185 | |||||||
| chr11:124796373 | A | G | 4 | a0001c0001t0004g0050 a0001c0001t0004g0051 a0001c0001t0004g0052 others(1): Show |
4 | HG02647.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+3498T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796373 | |||||||
| chr11:124796739 | T | A | 12 | a0001c0001t0001g0208 a0001c0001t0002g0184 a0001c0001t0002g0202 others(9): Show |
12 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+3132A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796739 | |||||||
| chr11:124796740 | C | T | 12 | a0001c0001t0001g0208 a0001c0001t0002g0184 a0001c0001t0002g0202 others(9): Show |
12 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+3131G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796740 | |||||||
| chr11:124796829 | T | A | 5 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0231 others(2): Show |
7 | HG02280.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+3042A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796829 | |||||||
| chr11:124796890 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510+2981C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124796890 | |||||||
| chr11:124797044 | T | G | 11 | a0001c0001t0002g0003 a0001c0001t0002g0083 a0001c0001t0002g0087 others(8): Show |
15 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+2827A>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797044 | |||||||
| chr11:124797199 | A | G | 11 | a0001c0001t0002g0003 a0001c0001t0002g0083 a0001c0001t0002g0087 others(8): Show |
15 | HG00642.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+2672T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797199 | |||||||
| chr11:124797222 | C | T | 1 | a0001c0001t0005g0219 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.510+2649G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797222 | |||||||
| chr11:124797358 | G | A | 1 | a0001c0001t0006g0167 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.510+2513C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797358 | |||||||
| chr11:124797455 | T | C | 71 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(68): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.510+2416A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797455 | |||||||
| chr11:124797478 | C | A | 71 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(68): Show |
82 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.510+2393G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797478 | |||||||
| chr11:124797522 | T | TA | 7 | a0001c0001t0001g0252 a0001c0001t0002g0014 a0001c0001t0004g0033 others(4): Show |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+2348dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797522 | |||||||
| chr11:124797523 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.510+2348T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797523 | |||||||
| chr11:124797550 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510+2321A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797550 | |||||||
| chr11:124797694 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.510+2177C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797694 | |||||||
| chr11:124797829 | A | G | 1 | a0001c0003t0002g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.510+2042T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797829 | |||||||
| chr11:124797946 | A | T | 12 | a0001c0001t0001g0208 a0001c0001t0002g0184 a0001c0001t0002g0202 others(9): Show |
12 | HG02615.hp2 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+1925T>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124797946 | |||||||
| chr11:124798234 | T | TA | 8 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0001g0172 others(5): Show |
8 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+1636dupT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAA | 8 | a0001c0001t0002g0182 a0001c0001t0003g0180 a0001c0001t0004g0179 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+1633_510+1636d others(6): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAA | 25 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0189 others(22): Show |
32 | HG00408.hp2 HG00423.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.510+1632_510+1636d others(7): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAA | 12 | a0001c0001t0001g0208 a0001c0001t0002g0046 a0001c0001t0002g0202 others(9): Show |
12 | HG01175.hp1 HG02027.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+1631_510+1636d others(8): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA | 10 | a0001c0001t0001g0215 a0001c0001t0002g0026 a0001c0001t0002g0047 others(7): Show |
11 | HG02559.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+1630_510+1636d others(9): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA others(1): Show |
10 | a0001c0001t0001g0221 a0001c0001t0002g0027 a0001c0001t0002g0028 others(7): Show |
12 | HG02683.hp2 HG02896.hp1 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+1629_510+1636d others(10): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA others(2): Show |
7 | a0001c0001t0001g0227 a0001c0001t0002g0029 a0001c0001t0002g0228 others(4): Show |
8 | HG02280.hp2 HG03540.hp1 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+1628_510+1636d others(11): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA others(3): Show |
3 | a0001c0001t0003g0233 a0001c0001t0003g0234 a0001c0001t0004g0235 |
3 | HG02109.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.510+1627_510+1636d others(12): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA others(4): Show |
5 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0003g0238 others(2): Show |
7 | HG01071.hp1 HG01109.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+1626_510+1636d others(13): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0239 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.510+1625_510+1636d others(14): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | TA | T | 22 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0090 others(19): Show |
28 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.510+1636delT | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | TAAAAAAA others(2): Show |
T | 7 | a0001c0001t0001g0252 a0001c0001t0002g0014 a0001c0001t0004g0033 others(4): Show |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+1628_510+1636d others(11): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | TAAAAAAA others(3): Show |
T | 14 | a0001c0001t0001g0250 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
19 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+1627_510+1636d others(12): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | TAAAAAAA others(4): Show |
T | 37 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(34): Show |
40 | HG00280.hp2 HG00544.hp1 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.510+1626_510+1636d others(13): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798234 | TAAAAAAA others(5): Show |
T | 1 | a0001c0001t0003g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.510+1625_510+1636d others(14): Show |
MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798234 | |||||||
| chr11:124798261 | T | A | 7 | a0001c0001t0002g0031 a0001c0001t0002g0239 a0001c0001t0003g0201 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+1610A>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798261 | |||||||
| chr11:124798315 | T | C | 2 | a0001c0001t0003g0240 a0001c0001t0003g0241 |
2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.510+1556A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798315 | |||||||
| chr11:124798335 | T | C | 1 | a0001c0001t0004g0242 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.510+1536A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798335 | |||||||
| chr11:124798409 | G | T | 59 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0066 others(56): Show |
70 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.510+1462C>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798409 | |||||||
| chr11:124798995 | A | C | 1 | a0001c0001t0003g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510+876T>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124798995 | |||||||
| chr11:124799040 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0012 a0001c0001t0002g0044 others(3): Show |
9 | HG00408.hp2 HG02129.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.510+831G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799040 | |||||||
| chr11:124799277 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510+594T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799277 | |||||||
| chr11:124799394 | T | C | 1 | a0001c0002t0002g0262 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.510+477A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799394 | |||||||
| chr11:124799434 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.510+437T>C | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799434 | |||||||
| chr11:124799456 | C | A | 3 | a0001c0001t0002g0243 a0001c0001t0002g0245 a0001c0001t0003g0244 |
3 | NA18979.hp1 NA19064.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.510+415G>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799456 | |||||||
| chr11:124799493 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.510+378G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799493 | |||||||
| chr11:124799503 | G | A | 13 | a0001c0001t0001g0250 a0001c0001t0002g0246 a0001c0001t0002g0247 others(10): Show |
18 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+368C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799503 | |||||||
| chr11:124799554 | G | C | 1 | a0001c0001t0001g0251 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.510+317C>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799554 | |||||||
| chr11:124799555 | G | A | 4 | a0001c0001t0001g0252 a0001c0001t0004g0033 a0001c0001t0004g0034 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+316C>T | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799555 | |||||||
| chr11:124799629 | T | C | 4 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0003g0256 others(1): Show |
4 | HG00140.hp1 HG00323.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+242A>G | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799629 | |||||||
| chr11:124799712 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | NA18967.hp2 NA19082.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.510+159G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799712 | |||||||
| chr11:124799768 | C | T | 1 | a0001c0001t0003g0038 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.510+103G>A | MSANTD2 | ENSG00000120458.13 | transcript | ENST00000374979.8 | protein_coding | 1/3 | chr11 | 124799768 |