Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91283 |
| ensemblid | ENSG00000066697.15 |
| hgncid | 23370 |
| symbol | MSANTD3 |
| name | Myb/SANT DNA binding domain containing 3 |
| refseq_nuc | NM_080655.3 |
| refseq_prot | NP_542386.1 |
| ensembl_nuc | ENST00000395067.7 |
| ensembl_prot | ENSP00000378506.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 100427143 |
| end | 100451734 |
| strand | + |
| ver | v1.2 |
| region | chr9:100427143-100451734 |
| region5000 | chr9:100422143-100456734 |
| regionname0 | MSANTD3_chr9_100427143_100451734 |
| regionname5000 | MSANTD3_chr9_100422143_100456734 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 275 | 326 | 90 | 55 | 125 | 12 | 42 | 90 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | MQNNE others(270): Show |
chr9 | 100422143 | 100456734 |
| a0002 | 0/0 | 275 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | MQNNE others(270): Show |
chr9 | 100422143 | 100456734 |
| a0003 | 0/0 | 275 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | MQNNE others(270): Show |
chr9 | 100422143 | 100456734 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 825 | 302 | 87 | 44 | 124 | 7 | 39 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | ATGCA others(820): Show |
chr9 | 100422143 | 100456734 | ||
| a0001c0002 | 0/1 | 825 | 23 | 3 | 11 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | ATGCA others(820): Show |
chr9 | 100422143 | 100456734 | ||
| a0001c0004 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | ATGCA others(820): Show |
chr9 | 100422143 | 100456734 | ||
| a0002c0003 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | ATGCA others(820): Show |
chr9 | 100422143 | 100456734 | ||
| a0003c0005 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | ATGCA others(820): Show |
chr9 | 100422143 | 100456734 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1879 | 149 | 36 | 23 | 71 | 3 | 16 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0002 | 0/0 | 1879 | 53 | 6 | 4 | 33 | 0 | 10 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0003 | 1/0 | 1880 | 53 | 15 | 8 | 19 | 2 | 8 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1875): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0004 | 0/0 | 1878 | 3 | 1 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0005 | 0/0 | 1878 | 12 | 12 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0006 | 0/0 | 1880 | 9 | 0 | 4 | 0 | 2 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1875): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0007 | 0/0 | 1879 | 7 | 7 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0008 | 0/0 | 1878 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0009 | 0/0 | 1878 | 2 | 1 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0010 | 0/0 | 1879 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0011 | 0/0 | 1879 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0012 | 0/0 | 1879 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0013 | 0/0 | 1879 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0014 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1875): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0016 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1875): Show |
chr9 | 100422143 | 100456734 |
| a0001c0001t0017 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0002t0004 | 0/1 | 1878 | 22 | 3 | 10 | 0 | 5 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1873): Show |
chr9 | 100422143 | 100456734 |
| a0001c0002t0015 | 0/0 | 1879 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0001c0004t0002 | 0/0 | 1879 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| a0002c0003t0006 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1875): Show |
chr9 | 100422143 | 100456734 |
| a0003c0005t0002 | 0/0 | 1879 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | CTCGG others(1874): Show |
chr9 | 100422143 | 100456734 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 1 | 13 | 1 | 5 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0002 | 0/0 | 13 | 3 | 0 | 9 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 3 | 2 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 0 | 3 | 1 | 3 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0017 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0007g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0008g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0009g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0010g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0011g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0013g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0014g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0001t0017g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0003 | 0/1 | 8 | 1 | 2 | 0 | 3 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0007 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0002t0015g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0001c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0002c0003t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| a0003c0005t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0003 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00140 | hp1 | a0001 | c0002 | t0004 | g0003 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0060 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00735 | hp2 | a0001 | c0002 | t0004 | g0171 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0134 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0145 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01069 | hp1 | a0001 | c0002 | t0004 | g0178 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0170 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01099 | hp2 | a0001 | c0001 | t0013 | g0160 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01169 | hp2 | a0001 | c0002 | t0015 | g0167 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01192 | hp1 | a0001 | c0001 | t0013 | g0034 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01192 | hp2 | a0001 | c0002 | t0004 | g0173 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0123 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01361 | hp2 | a0001 | c0002 | t0004 | g0174 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0017 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01516 | hp2 | a0001 | c0002 | t0004 | g0003 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0017 | EUR | IBS | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01975 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0179 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02602 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0175 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0133 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03041 | hp1 | a0001 | c0001 | t0012 | g0104 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0061 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0056 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0210 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0057 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0003 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | ESN | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0050 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0211 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03669 | hp1 | a0001 | c0002 | t0004 | g0176 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0131 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0040 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0114 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0208 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | STU | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0111 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18747 | hp1 | a0003 | c0005 | t0002 | g0193 | EAS | CHB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0069 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19004 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19030 | hp2 | a0001 | c0001 | t0014 | g0058 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | YRI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | ASW | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0168 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0007 | EUR | TSI | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | GIH | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01123 | hp1 | a0001 | c0002 | t0004 | g0003 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG01123 | hp2 | a0002 | c0003 | t0006 | g0065 | AMR | CLM | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02559 | hp1 | a0001 | c0002 | t0004 | g0003 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | USA | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0007 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0004 | g0003 | REF | REF | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0108 | REF | REF | MSANTD3_chr9_100422143_100456734 | MSANTD3 | chr9 | 100422143 | 100456734 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100442254 | C | G | 1 | a0003 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.316C>G | p.Leu106Val | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 600/1880 | 316/828 | 106/275 | chr9 | 100442254 | |||
| chr9:100450728 | A | G | 1 | a0002 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.590A>G | p.His197Arg | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 874/1880 | 590/828 | 197/275 | chr9 | 100450728 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100442295 | C | G | 1 | a0001c0002 | 22 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(19): Show |
synonymous_variant | LOW | c.357C>G | p.Leu119Leu | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 641/1880 | 357/828 | 119/275 | chr9 | 100442295 | |||
| chr9:100442340 | C | T | 1 | a0001c0004 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.402C>T | p.Pro134Pro | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/3 | 686/1880 | 402/828 | 134/275 | chr9 | 100442340 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100427257 | C | T | 1 | a0001c0001t0005 | 12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-170C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | chr9 | 100427257 | |||||||
| chr9:100427278 | T | C | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(10): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-149T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14661 | chr9 | 100427278 | ||||||
| chr9:100427280 | C | T | 1 | a0001c0001t0013 | 2 | HG01099.hp2 HG01192.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-147C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | chr9 | 100427280 | |||||||
| chr9:100427313 | G | A | 1 | a0001c0001t0009 | 2 | HG00733.hp1 HG03098.hp1 |
5_prime_UTR_variant | MODIFIER | c.-114G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14626 | chr9 | 100427313 | ||||||
| chr9:100427325 | C | T | 4 | a0001c0001t0002 a0001c0001t0016 a0001c0004t0002 others(1): Show |
56 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(53): Show |
5_prime_UTR_variant | MODIFIER | c.-102C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/3 | 14614 | chr9 | 100427325 | ||||||
| chr9:100451232 | C | T | 3 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0015 |
25 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*266C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 266 | chr9 | 100451232 | ||||||
| chr9:100451258 | T | TG | 1 | a0001c0001t0007 | 7 | HG01891.hp1 HG02280.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*292_*293insG | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 293 | chr9 | 100451258 | ||||||
| chr9:100451305 | AT | A | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(12): Show |
260 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(257): Show |
3_prime_UTR_variant | MODIFIER | c.*352delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 352 | INFO_REALIGN_3_PRIME | chr9 | 100451305 | |||||
| chr9:100451374 | A | G | 2 | a0001c0001t0007 a0001c0001t0009 |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*408A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 408 | chr9 | 100451374 | ||||||
| chr9:100451413 | A | G | 1 | a0001c0001t0011 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 447 | chr9 | 100451413 | ||||||
| chr9:100451461 | C | T | 1 | a0001c0001t0006 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*495C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 495 | chr9 | 100451461 | ||||||
| chr9:100451663 | G | A | 1 | a0001c0001t0009 | 2 | HG00733.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*697G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 697 | chr9 | 100451663 | ||||||
| chr9:100451665 | A | G | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(16): Show |
272 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 699 | chr9 | 100451665 | ||||||
| chr9:100451711 | TA | T | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(5): Show |
51 | HG00099.hp1 HG00140.hp1 HG00733.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*759delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 3/3 | 759 | INFO_REALIGN_3_PRIME | chr9 | 100451711 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100427426 | C | CGGGCGG | 7 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
8 | HG01069.hp2 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+43_-34+48dupCG others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100427426 | ||||||
| chr9:100427461 | G | C | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-34+68G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427461 | |||||||
| chr9:100427468 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-34+75G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427468 | |||||||
| chr9:100427769 | C | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+376C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427769 | |||||||
| chr9:100427896 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-34+503C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100427896 | |||||||
| chr9:100428051 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-34+658G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428051 | |||||||
| chr9:100428112 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-34+719C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428112 | |||||||
| chr9:100428174 | A | G | 37 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(34): Show |
58 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-34+781A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428174 | |||||||
| chr9:100428392 | CAT | C | 3 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0057 |
3 | HG03098.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-34+1001_-34+1002d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100428392 | ||||||
| chr9:100428433 | A | G | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+1040A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428433 | |||||||
| chr9:100428490 | G | A | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+1097G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428490 | |||||||
| chr9:100428666 | G | C | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+1273G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428666 | |||||||
| chr9:100428785 | A | G | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+1392A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428785 | |||||||
| chr9:100428966 | A | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34+1573A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100428966 | |||||||
| chr9:100429011 | C | T | 1 | a0001c0001t0011g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-34+1618C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429011 | |||||||
| chr9:100429045 | G | A | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+1652G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429045 | |||||||
| chr9:100429084 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+1691G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429084 | |||||||
| chr9:100429179 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 |
6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+1786A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429179 | |||||||
| chr9:100429194 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-34+1801G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429194 | |||||||
| chr9:100429707 | G | GT | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(5): Show |
8 | HG00438.hp2 HG01099.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+2324dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100429707 | ||||||
| chr9:100429707 | GT | G | 19 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(16): Show |
29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-34+2324delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100429707 | ||||||
| chr9:100429720 | G | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+2327G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429720 | |||||||
| chr9:100429777 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-34+2384A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429777 | |||||||
| chr9:100429782 | A | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0157 a0001c0001t0003g0158 |
5 | NA18954.hp1 NA18989.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+2389A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429782 | |||||||
| chr9:100429992 | C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+2599C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100429992 | |||||||
| chr9:100430081 | TCTC | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+2692_-34+2694d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430081 | ||||||
| chr9:100430095 | C | CA | 30 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0183 others(27): Show |
41 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-34+2721dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430095 | ||||||
| chr9:100430095 | CA | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0156 a0001c0001t0002g0206 others(3): Show |
7 | HG02165.hp1 HG02165.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+2721delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430095 | ||||||
| chr9:100430260 | A | C | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+2867A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430260 | |||||||
| chr9:100430270 | G | A | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+2877G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430270 | |||||||
| chr9:100430324 | C | CA | 48 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0165 others(45): Show |
76 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-34+2949dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | ||||||
| chr9:100430324 | C | CAA | 6 | a0001c0001t0002g0184 a0001c0001t0002g0206 a0001c0001t0007g0006 others(3): Show |
11 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+2948_-34+2949d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | ||||||
| chr9:100430324 | CA | C | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(18): Show |
31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-34+2949delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100430324 | ||||||
| chr9:100430341 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-34+2948A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430341 | |||||||
| chr9:100430403 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+3010G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430403 | |||||||
| chr9:100430469 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0149 a0001c0001t0001g0150 |
4 | HG01884.hp2 HG02258.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+3076A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430469 | |||||||
| chr9:100430825 | T | C | 4 | a0001c0001t0003g0026 a0001c0001t0003g0073 a0001c0001t0003g0074 others(1): Show |
5 | HG02145.hp1 HG02723.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+3432T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430825 | |||||||
| chr9:100430858 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-34+3465A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430858 | |||||||
| chr9:100430861 | G | A | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+3468G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430861 | |||||||
| chr9:100430963 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-34+3570G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100430963 | |||||||
| chr9:100431024 | T | C | 64 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(61): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+3631T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431024 | |||||||
| chr9:100431071 | C | T | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+3678C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431071 | |||||||
| chr9:100431079 | C | T | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-34+3686C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431079 | |||||||
| chr9:100431301 | C | CT | 9 | a0001c0001t0001g0052 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG00741.hp1 HG01884.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.-34+3927dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | ||||||
| chr9:100431301 | CT | C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0077 a0001c0001t0001g0078 others(36): Show |
57 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-34+3927delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | ||||||
| chr9:100431301 | CTT | C | 6 | a0001c0001t0001g0165 a0001c0001t0007g0006 a0001c0001t0007g0062 others(3): Show |
11 | HG00733.hp1 HG01081.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+3926_-34+3927d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431301 | ||||||
| chr9:100431425 | C | T | 1 | a0001c0001t0003g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-34+4032C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431425 | |||||||
| chr9:100431546 | T | TC | 75 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-34+4158dupC | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431546 | ||||||
| chr9:100431614 | C | CT | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+4230dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100431614 | ||||||
| chr9:100431667 | T | A | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+4274T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431667 | |||||||
| chr9:100431825 | G | A | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+4432G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431825 | |||||||
| chr9:100431832 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+4439G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100431832 | |||||||
| chr9:100432187 | G | C | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG02145.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+4794G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432187 | |||||||
| chr9:100432228 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-34+4835G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432228 | |||||||
| chr9:100432245 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-34+4852G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432245 | |||||||
| chr9:100432248 | A | C | 1 | a0001c0001t0005g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+4855A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432248 | |||||||
| chr9:100432357 | A | G | 3 | a0001c0001t0003g0141 a0001c0001t0003g0142 a0001c0001t0003g0148 |
3 | HG00741.hp2 HG01099.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-34+4964A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432357 | |||||||
| chr9:100432457 | G | A | 20 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(17): Show |
30 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+5064G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432457 | |||||||
| chr9:100432474 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0155 |
2 | HG01952.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-34+5081G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432474 | |||||||
| chr9:100432787 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-34+5394T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100432787 | |||||||
| chr9:100433086 | A | C | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+5693A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433086 | |||||||
| chr9:100433135 | G | A | 1 | a0001c0001t0002g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-34+5742G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433135 | |||||||
| chr9:100433272 | A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+5879A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433272 | |||||||
| chr9:100433431 | A | G | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0080 others(2): Show |
6 | HG01099.hp2 HG01192.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+6038A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433431 | |||||||
| chr9:100433451 | C | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6058C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433451 | |||||||
| chr9:100433505 | G | A | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34+6112G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433505 | |||||||
| chr9:100433510 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 |
6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+6117T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433510 | |||||||
| chr9:100433644 | T | G | 64 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(61): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-34+6251T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433644 | |||||||
| chr9:100433820 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-34+6427C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433820 | |||||||
| chr9:100433859 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-34+6466G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433859 | |||||||
| chr9:100433872 | G | A | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6479G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433872 | |||||||
| chr9:100433929 | G | A | 75 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-34+6536G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433929 | |||||||
| chr9:100433977 | G | A | 15 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(12): Show |
25 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-34+6584G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100433977 | |||||||
| chr9:100434016 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-34+6623C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434016 | |||||||
| chr9:100434106 | A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+6713A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434106 | |||||||
| chr9:100434124 | A | G | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-34+6731A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434124 | |||||||
| chr9:100434192 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34+6799A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434192 | |||||||
| chr9:100434286 | G | A | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+6893G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434286 | |||||||
| chr9:100434458 | A | C | 1 | a0001c0001t0003g0164 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-34+7065A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434458 | |||||||
| chr9:100434508 | C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+7115C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434508 | |||||||
| chr9:100434542 | G | GA | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-34+7152dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434542 | ||||||
| chr9:100434621 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 |
6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7228T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434621 | |||||||
| chr9:100434970 | T | TAC | 12 | a0001c0001t0001g0022 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
16 | HG01069.hp2 HG01074.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33-6917_-33-6916d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | ||||||
| chr9:100434970 | T | TACAC | 2 | a0001c0001t0005g0023 a0001c0001t0005g0047 |
3 | HG01891.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-33-6919_-33-6916d others(6): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | ||||||
| chr9:100434970 | TAC | T | 19 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(16): Show |
29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-6917_-33-6916d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100434970 | ||||||
| chr9:100434987 | A | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0208 a0001c0001t0010g0040 |
5 | HG02602.hp1 HG03834.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-6919A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434987 | |||||||
| chr9:100434989 | A | G | 61 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(58): Show |
97 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-33-6917A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434989 | |||||||
| chr9:100434992 | T | C | 62 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(59): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.-33-6914T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100434992 | |||||||
| chr9:100435007 | T | A | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6899T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435007 | |||||||
| chr9:100435116 | G | A | 2 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-33-6790G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435116 | |||||||
| chr9:100435242 | C | T | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-6664C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435242 | |||||||
| chr9:100435295 | A | G | 38 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(35): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-33-6611A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435295 | |||||||
| chr9:100435358 | C | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-6548C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435358 | |||||||
| chr9:100435503 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-33-6403T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435503 | |||||||
| chr9:100435597 | G | A | 1 | a0001c0001t0003g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-33-6309G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435597 | |||||||
| chr9:100435601 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-33-6305T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435601 | |||||||
| chr9:100435665 | G | A | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6241G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435665 | |||||||
| chr9:100435685 | T | C | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-6221T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435685 | |||||||
| chr9:100435709 | A | G | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-6197A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435709 | |||||||
| chr9:100435968 | A | C | 1 | a0001c0001t0002g0201 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-33-5938A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100435968 | |||||||
| chr9:100436166 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-33-5740C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436166 | |||||||
| chr9:100436453 | C | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-33-5453C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436453 | |||||||
| chr9:100436464 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-5442C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436464 | |||||||
| chr9:100436471 | A | G | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-5435A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436471 | |||||||
| chr9:100436645 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-33-5261G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436645 | |||||||
| chr9:100436738 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-5168G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436738 | |||||||
| chr9:100436805 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-33-5101C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436805 | |||||||
| chr9:100436835 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-33-5071C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436835 | |||||||
| chr9:100436868 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-33-5038G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436868 | |||||||
| chr9:100436891 | G | A | 1 | a0001c0001t0009g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-33-5015G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436891 | |||||||
| chr9:100436964 | C | G | 1 | a0001c0001t0003g0041 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33-4942C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100436964 | |||||||
| chr9:100437002 | G | A | 19 | a0001c0001t0002g0188 a0001c0001t0004g0169 a0001c0001t0004g0170 others(16): Show |
29 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33-4904G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437002 | |||||||
| chr9:100437016 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 |
6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-4890G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437016 | |||||||
| chr9:100437321 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-33-4585A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437321 | |||||||
| chr9:100437404 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0136 others(2): Show |
8 | NA18940.hp1 NA18946.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-4502C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437404 | |||||||
| chr9:100437683 | T | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-4223T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437683 | |||||||
| chr9:100437712 | A | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-4194A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437712 | |||||||
| chr9:100437976 | T | G | 1 | a0001c0001t0002g0207 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-33-3930T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100437976 | |||||||
| chr9:100438305 | C | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-3601C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438305 | |||||||
| chr9:100438317 | A | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-3589A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438317 | |||||||
| chr9:100438333 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-33-3573A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438333 | |||||||
| chr9:100438427 | A | AGT | 11 | a0001c0001t0001g0059 a0001c0001t0001g0132 a0001c0001t0001g0138 others(8): Show |
13 | HG00642.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33-3462_-33-3461d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100438427 | ||||||
| chr9:100438427 | A | AGTGTGTG others(1): Show |
18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-3468_-33-3461d others(10): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100438427 | ||||||
| chr9:100438430 | G | A | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-3476G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438430 | |||||||
| chr9:100438431 | T | A | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-3475T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438431 | |||||||
| chr9:100438611 | G | A | 2 | a0001c0001t0009g0060 a0001c0001t0009g0061 |
2 | HG00733.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-33-3295G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438611 | |||||||
| chr9:100438638 | G | A | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-33-3268G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438638 | |||||||
| chr9:100438759 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-33-3147G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100438759 | |||||||
| chr9:100439128 | A | T | 2 | a0001c0002t0004g0175 a0001c0002t0004g0176 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-33-2778A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439128 | |||||||
| chr9:100439179 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33-2727A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439179 | |||||||
| chr9:100439372 | T | C | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-2534T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439372 | |||||||
| chr9:100439515 | T | A | 68 | a0001c0001t0001g0183 a0001c0001t0002g0002 a0001c0001t0002g0019 others(65): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-33-2391T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439515 | |||||||
| chr9:100439518 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-33-2388T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439518 | |||||||
| chr9:100439604 | G | A | 1 | a0001c0001t0004g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33-2302G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439604 | |||||||
| chr9:100439605 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0093 a0001c0001t0001g0126 others(2): Show |
8 | HG02258.hp2 HG02615.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-2301G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439605 | |||||||
| chr9:100439676 | A | AT | 9 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0162 others(6): Show |
11 | HG00544.hp1 HG01070.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-2214dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100439676 | ||||||
| chr9:100439785 | C | T | 2 | a0001c0001t0003g0091 a0001c0001t0003g0092 |
2 | NA18983.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-33-2121C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439785 | |||||||
| chr9:100439953 | A | C | 1 | a0001c0001t0001g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33-1953A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439953 | |||||||
| chr9:100439969 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0198 a0001c0001t0002g0205 |
4 | HG00408.hp2 NA18747.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-1937A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100439969 | |||||||
| chr9:100440017 | G | A | 1 | a0001c0001t0003g0096 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-33-1889G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440017 | |||||||
| chr9:100440073 | G | C | 2 | a0001c0001t0003g0063 a0001c0001t0003g0097 |
2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-33-1833G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440073 | |||||||
| chr9:100440210 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0130 |
3 | HG01255.hp2 HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-33-1696G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440210 | |||||||
| chr9:100440232 | G | C | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-1674G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440232 | |||||||
| chr9:100440241 | C | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-1665C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440241 | |||||||
| chr9:100440308 | T | C | 75 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(72): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.-33-1598T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440308 | |||||||
| chr9:100440330 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-33-1576T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440330 | |||||||
| chr9:100440510 | T | G | 5 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0100 others(2): Show |
5 | HG02129.hp2 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1396T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440510 | |||||||
| chr9:100440585 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-33-1321G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440585 | |||||||
| chr9:100440587 | C | CA | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-1316dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440587 | ||||||
| chr9:100440590 | A | AT | 9 | a0001c0001t0001g0016 a0001c0001t0001g0045 a0001c0001t0001g0086 others(6): Show |
11 | HG01074.hp2 HG01255.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-33-1297dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440590 | ||||||
| chr9:100440590 | AT | A | 63 | a0001c0001t0001g0082 a0001c0001t0001g0103 a0001c0001t0001g0183 others(60): Show |
94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-33-1297delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440590 | ||||||
| chr9:100440591 | T | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-1315T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440591 | |||||||
| chr9:100440592 | T | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-1314T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440592 | |||||||
| chr9:100440722 | C | G | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.-33-1184C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440722 | |||||||
| chr9:100440780 | C | CT | 60 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0033 others(57): Show |
87 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-33-1099dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | ||||||
| chr9:100440780 | C | CTT | 16 | a0001c0001t0001g0044 a0001c0001t0001g0183 a0001c0001t0001g0186 others(13): Show |
18 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-1100_-33-1099d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | ||||||
| chr9:100440780 | C | CTTT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0053 a0001c0001t0001g0120 others(2): Show |
7 | HG00558.hp2 HG00621.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-1101_-33-1099d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | ||||||
| chr9:100440780 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-33-1126C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440780 | |||||||
| chr9:100440780 | CT | C | 9 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
13 | HG00733.hp1 HG01256.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-1099delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | ||||||
| chr9:100440780 | CTTTTTT | C | 16 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(13): Show |
26 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-33-1104_-33-1099d others(8): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440780 | ||||||
| chr9:100440806 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-33-1100T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440806 | |||||||
| chr9:100440921 | G | A | 1 | a0001c0001t0011g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-33-985G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100440921 | |||||||
| chr9:100440931 | C | CT | 28 | a0001c0001t0001g0032 a0001c0001t0001g0059 a0001c0001t0001g0093 others(25): Show |
34 | HG00438.hp2 HG00733.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.-33-953dupT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440931 | ||||||
| chr9:100440931 | CT | C | 21 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0072 others(18): Show |
32 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.-33-953delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100440931 | ||||||
| chr9:100441000 | A | G | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-906A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441000 | |||||||
| chr9:100441355 | C | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-551C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441355 | |||||||
| chr9:100441444 | C | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33-462C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441444 | |||||||
| chr9:100441544 | C | T | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-362C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441544 | |||||||
| chr9:100441635 | G | A | 3 | a0001c0001t0005g0023 a0001c0001t0005g0024 a0001c0001t0005g0047 |
5 | HG01891.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-271G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | chr9 | 100441635 | |||||||
| chr9:100441639 | C | CA | 8 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(5): Show |
12 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33-257dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr9 | 100441639 | ||||||
| chr9:100442362 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.418+6C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442362 | |||||||
| chr9:100442513 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.418+157A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442513 | |||||||
| chr9:100442543 | G | A | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+187G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442543 | |||||||
| chr9:100442808 | C | CA | 18 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0071 others(15): Show |
20 | HG00735.hp2 HG00741.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.418+473dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | ||||||
| chr9:100442808 | CA | C | 6 | a0001c0001t0001g0077 a0001c0001t0002g0180 a0001c0001t0002g0206 others(3): Show |
11 | HG01891.hp1 HG02056.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+473delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | ||||||
| chr9:100442808 | CAA | C | 37 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(34): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.418+472_418+473del others(2): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100442808 | ||||||
| chr9:100442979 | A | C | 1 | a0001c0001t0002g0197 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.418+623A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100442979 | |||||||
| chr9:100443042 | A | C | 3 | a0001c0001t0008g0055 a0001c0001t0008g0056 a0001c0001t0008g0057 |
3 | HG03098.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.418+686A>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443042 | |||||||
| chr9:100443117 | C | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+761C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443117 | |||||||
| chr9:100443215 | C | T | 1 | a0001c0001t0012g0104 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.418+859C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443215 | |||||||
| chr9:100443329 | G | T | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.418+973G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443329 | |||||||
| chr9:100443372 | G | C | 72 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(69): Show |
112 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.418+1016G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443372 | |||||||
| chr9:100443395 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(214): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.418+1039A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443395 | |||||||
| chr9:100443399 | CA | C | 20 | a0001c0001t0001g0209 a0001c0001t0002g0196 a0001c0001t0004g0169 others(17): Show |
31 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.418+1057delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100443399 | ||||||
| chr9:100443403 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.418+1047A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443403 | |||||||
| chr9:100443471 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.418+1115G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443471 | |||||||
| chr9:100443581 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.418+1225T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443581 | |||||||
| chr9:100443621 | A | G | 1 | a0001c0001t0006g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.418+1265A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443621 | |||||||
| chr9:100443677 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.418+1321G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443677 | |||||||
| chr9:100443742 | G | A | 38 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(35): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.418+1386G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443742 | |||||||
| chr9:100443778 | T | G | 1 | a0001c0001t0001g0033 | 2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.418+1422T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443778 | |||||||
| chr9:100443807 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0107 |
2 | NA19002.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.418+1451A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443807 | |||||||
| chr9:100443901 | C | T | 1 | a0001c0001t0014g0058 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+1545C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100443901 | |||||||
| chr9:100444048 | G | A | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+1692G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444048 | |||||||
| chr9:100444133 | C | T | 8 | a0001c0001t0003g0004 a0001c0001t0003g0018 a0001c0001t0003g0031 others(5): Show |
17 | HG00140.hp2 HG00735.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.418+1777C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444133 | |||||||
| chr9:100444137 | C | A | 10 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
13 | HG00558.hp2 HG00621.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.418+1781C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444137 | |||||||
| chr9:100444370 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.418+2014G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444370 | |||||||
| chr9:100444708 | G | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0046 others(2): Show |
7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+2352G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444708 | |||||||
| chr9:100444748 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 |
6 | HG01081.hp2 HG01243.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+2392T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444748 | |||||||
| chr9:100444760 | C | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.418+2404C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444760 | |||||||
| chr9:100444912 | C | T | 1 | a0001c0001t0010g0040 | 2 | HG02602.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.418+2556C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100444912 | |||||||
| chr9:100445001 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0159 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.418+2645C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445001 | |||||||
| chr9:100445098 | AGGTAGGG others(4): Show |
A | 1 | a0001c0001t0003g0092 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.418+2747_418+2757d others(13): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100445098 | ||||||
| chr9:100445213 | C | T | 1 | a0001c0001t0003g0076 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.418+2857C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445213 | |||||||
| chr9:100445372 | G | A | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+3016G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445372 | |||||||
| chr9:100445427 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.418+3071A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445427 | |||||||
| chr9:100445709 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.418+3353T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445709 | |||||||
| chr9:100445727 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.418+3371A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445727 | |||||||
| chr9:100445788 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.418+3432G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445788 | |||||||
| chr9:100445849 | C | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+3493C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445849 | |||||||
| chr9:100445860 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.418+3504G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100445860 | |||||||
| chr9:100446007 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3651C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446007 | |||||||
| chr9:100446010 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3654C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446010 | |||||||
| chr9:100446011 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3655C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446011 | |||||||
| chr9:100446015 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3659A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446015 | |||||||
| chr9:100446016 | T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3660T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446016 | |||||||
| chr9:100446017 | T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3661T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446017 | |||||||
| chr9:100446020 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3664G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446020 | |||||||
| chr9:100446022 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3666G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446022 | |||||||
| chr9:100446023 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3667G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446023 | |||||||
| chr9:100446024 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3668G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446024 | |||||||
| chr9:100446025 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3669C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446025 | |||||||
| chr9:100446027 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3671A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446027 | |||||||
| chr9:100446028 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3672C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446028 | |||||||
| chr9:100446030 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3674G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446030 | |||||||
| chr9:100446032 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3676G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446032 | |||||||
| chr9:100446035 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3679C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446035 | |||||||
| chr9:100446036 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3680A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446036 | |||||||
| chr9:100446037 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3681G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446037 | |||||||
| chr9:100446038 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3682A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446038 | |||||||
| chr9:100446039 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3683A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446039 | |||||||
| chr9:100446040 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3684C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446040 | |||||||
| chr9:100446041 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3685C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446041 | |||||||
| chr9:100446044 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3688C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446044 | |||||||
| chr9:100446050 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3694G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446050 | |||||||
| chr9:100446052 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3696G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446052 | |||||||
| chr9:100446053 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3697C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446053 | |||||||
| chr9:100446054 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3698C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446054 | |||||||
| chr9:100446056 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3700A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446056 | |||||||
| chr9:100446060 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3704A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446060 | |||||||
| chr9:100446061 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3705A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446061 | |||||||
| chr9:100446064 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3708C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446064 | |||||||
| chr9:100446065 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3709G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446065 | |||||||
| chr9:100446066 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3710C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446066 | |||||||
| chr9:100446069 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3713G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446069 | |||||||
| chr9:100446070 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3714G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446070 | |||||||
| chr9:100446071 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3715A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446071 | |||||||
| chr9:100446072 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3716G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446072 | |||||||
| chr9:100446074 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3718G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446074 | |||||||
| chr9:100446075 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3719G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446075 | |||||||
| chr9:100446076 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3720C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446076 | |||||||
| chr9:100446078 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3722G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446078 | |||||||
| chr9:100446079 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3723G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446079 | |||||||
| chr9:100446080 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3724G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446080 | |||||||
| chr9:100446082 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3726G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446082 | |||||||
| chr9:100446083 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3727G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446083 | |||||||
| chr9:100446084 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3728C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446084 | |||||||
| chr9:100446087 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3731G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446087 | |||||||
| chr9:100446088 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3732G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446088 | |||||||
| chr9:100446089 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3733A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446089 | |||||||
| chr9:100446091 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3735G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446091 | |||||||
| chr9:100446093 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3737C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446093 | |||||||
| chr9:100446094 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3738C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446094 | |||||||
| chr9:100446099 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3743G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446099 | |||||||
| chr9:100446101 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3745C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446101 | |||||||
| chr9:100446102 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3746A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446102 | |||||||
| chr9:100446114 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3758G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446114 | |||||||
| chr9:100446117 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3761A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446117 | |||||||
| chr9:100446118 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3762A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446118 | |||||||
| chr9:100446119 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3763C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446119 | |||||||
| chr9:100446121 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3765A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446121 | |||||||
| chr9:100446122 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3766A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446122 | |||||||
| chr9:100446123 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3767G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446123 | |||||||
| chr9:100446124 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3768C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446124 | |||||||
| chr9:100446129 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3773G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446129 | |||||||
| chr9:100446131 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3775G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446131 | |||||||
| chr9:100446133 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3777A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446133 | |||||||
| chr9:100446134 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3778G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446134 | |||||||
| chr9:100446135 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3779C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446135 | |||||||
| chr9:100446137 | C | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3781C>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446137 | |||||||
| chr9:100446138 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3782C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446138 | |||||||
| chr9:100446141 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3785G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446141 | |||||||
| chr9:100446142 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3786A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446142 | |||||||
| chr9:100446144 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3788G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446144 | |||||||
| chr9:100446146 | C | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3790C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446146 | |||||||
| chr9:100446148 | T | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3792T>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446148 | |||||||
| chr9:100446150 | G | A | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3794G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446150 | |||||||
| chr9:100446151 | G | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3795G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446151 | |||||||
| chr9:100446152 | A | T | 1 | a0001c0002t0004g0179 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.418+3796A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446152 | |||||||
| chr9:100446178 | A | G | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+3822A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446178 | |||||||
| chr9:100446224 | G | A | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.418+3868G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446224 | |||||||
| chr9:100446364 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.418+4008A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446364 | |||||||
| chr9:100446414 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0136 others(2): Show |
8 | NA18940.hp1 NA18946.hp1 NA18970.hp1 others(5): Show |
intron_variant | MODIFIER | c.418+4058C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446414 | |||||||
| chr9:100446417 | G | A | 18 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0081 others(15): Show |
19 | HG01255.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.418+4061G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446417 | |||||||
| chr9:100446653 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.419-3904C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100446653 | |||||||
| chr9:100446825 | T | TA | 65 | a0001c0001t0001g0138 a0001c0001t0001g0183 a0001c0001t0001g0186 others(62): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.419-3717dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100446825 | ||||||
| chr9:100446825 | T | TAA | 11 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(8): Show |
18 | HG01081.hp2 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.419-3718_419-3717d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100446825 | ||||||
| chr9:100447040 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.419-3517C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447040 | |||||||
| chr9:100447319 | C | T | 1 | a0003c0005t0002g0193 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.419-3238C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447319 | |||||||
| chr9:100447368 | CT | C | 76 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(73): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.419-3180delT | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100447368 | ||||||
| chr9:100447453 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.419-3104G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100447453 | |||||||
| chr9:100448059 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.419-2498G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448059 | |||||||
| chr9:100448092 | G | A | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.419-2465G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448092 | |||||||
| chr9:100448098 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.419-2459G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448098 | |||||||
| chr9:100448143 | A | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0198 a0001c0001t0002g0205 |
4 | HG00408.hp2 NA18747.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-2414A>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448143 | |||||||
| chr9:100448190 | C | CA | 47 | a0001c0001t0001g0028 a0001c0001t0001g0052 a0001c0001t0001g0081 others(44): Show |
64 | HG00408.hp2 HG00621.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.419-2343dupA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | ||||||
| chr9:100448190 | C | CAA | 11 | a0001c0001t0002g0021 a0001c0001t0002g0039 a0001c0001t0002g0194 others(8): Show |
20 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.419-2344_419-2343d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | ||||||
| chr9:100448190 | CA | C | 18 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0035 others(15): Show |
27 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-2343delA | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | ||||||
| chr9:100448190 | CAA | C | 18 | a0001c0001t0004g0169 a0001c0001t0004g0172 a0001c0001t0005g0012 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.419-2344_419-2343d others(4): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448190 | ||||||
| chr9:100448212 | A | AG | 5 | a0001c0001t0002g0019 a0001c0001t0002g0182 a0001c0001t0002g0192 others(2): Show |
7 | HG00423.hp1 HG00544.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.419-2345_419-2344i others(3): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448212 | |||||||
| chr9:100448283 | G | A | 1 | a0001c0002t0004g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.419-2274G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448283 | |||||||
| chr9:100448310 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-2247A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448310 | |||||||
| chr9:100448491 | G | C | 2 | a0001c0001t0011g0210 a0001c0001t0011g0211 |
2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.419-2066G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448491 | |||||||
| chr9:100448536 | G | A | 38 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(35): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.419-2021G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448536 | |||||||
| chr9:100448805 | C | T | 1 | a0001c0001t0006g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.419-1752C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100448805 | |||||||
| chr9:100448951 | CAGT | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(1): Show |
9 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.419-1603_419-1601d others(5): Show |
MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr9 | 100448951 | ||||||
| chr9:100449043 | C | T | 73 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(70): Show |
113 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.419-1514C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449043 | |||||||
| chr9:100449052 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(6): Show |
13 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-1505C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449052 | |||||||
| chr9:100449065 | T | C | 1 | a0001c0001t0011g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.419-1492T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449065 | |||||||
| chr9:100449111 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.419-1446G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449111 | |||||||
| chr9:100449114 | C | T | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.419-1443C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449114 | |||||||
| chr9:100449163 | C | G | 1 | a0001c0001t0003g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.419-1394C>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449163 | |||||||
| chr9:100449163 | C | T | 1 | a0001c0001t0003g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.419-1394C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449163 | |||||||
| chr9:100449235 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.419-1322C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449235 | |||||||
| chr9:100449325 | C | T | 1 | a0001c0001t0004g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-1232C>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449325 | |||||||
| chr9:100449345 | A | G | 1 | a0001c0001t0002g0184 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.419-1212A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449345 | |||||||
| chr9:100449520 | T | G | 76 | a0001c0001t0001g0011 a0001c0001t0001g0165 a0001c0001t0001g0166 others(73): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.419-1037T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449520 | |||||||
| chr9:100449695 | G | A | 38 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(35): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.419-862G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449695 | |||||||
| chr9:100449741 | G | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0023 a0001c0001t0005g0024 others(6): Show |
13 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.419-816G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449741 | |||||||
| chr9:100449757 | T | C | 18 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0172 others(15): Show |
28 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.419-800T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449757 | |||||||
| chr9:100449827 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.419-730A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449827 | |||||||
| chr9:100449875 | T | G | 1 | a0001c0001t0011g0210 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.419-682T>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100449875 | |||||||
| chr9:100450081 | G | C | 3 | a0001c0001t0003g0073 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | HG02145.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.419-476G>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450081 | |||||||
| chr9:100450246 | T | C | 39 | a0001c0001t0001g0183 a0001c0001t0001g0186 a0001c0001t0002g0002 others(36): Show |
60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.419-311T>C | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450246 | |||||||
| chr9:100450446 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.419-111A>G | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450446 | |||||||
| chr9:100450462 | G | A | 6 | a0001c0001t0007g0006 a0001c0001t0007g0062 a0001c0001t0009g0060 others(3): Show |
11 | HG00733.hp1 HG01891.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.419-95G>A | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450462 | |||||||
| chr9:100450491 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0161 |
3 | HG02738.hp1 HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.419-66G>T | MSANTD3 | ENSG00000066697.15 | transcript | ENST00000395067.7 | protein_coding | 2/2 | chr9 | 100450491 |