Item | Value |
---|---|
geneid | 10232 |
ensemblid | ENSG00000102854.16 |
hgncid | 7371 |
symbol | MSLN |
name | mesothelin |
refseq_nuc | NM_005823.6 |
refseq_prot | NP_005814.2 |
ensembl_nuc | ENST00000545450.7 |
ensembl_prot | ENSP00000442965.2 |
mane_status | MANE Select |
chr | chr16 |
start | 760734 |
end | 768862 |
strand | + |
ver | v1.2 |
region | chr16:760734-768862 |
region5000 | chr16:755734-773862 |
regionname0 | MSLN_chr16_760734_768862 |
regionname5000 | MSLN_chr16_755734_773862 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 622 | 161 | 21 | 30 | 86 | 7 | 16 | 62 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0002 | 0/1 | 622 | 98 | 22 | 19 | 45 | 2 | 9 | 34 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0003 | 0/0 | 622 | 23 | 14 | 2 | 3 | 1 | 3 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0004 | 0/0 | 622 | 17 | 0 | 1 | 9 | 0 | 7 | 6 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0005 | 0/0 | 622 | 17 | 2 | 3 | 4 | 0 | 8 | 4 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0006 | 0/0 | 622 | 14 | 11 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0007 | 0/0 | 622 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0008 | 0/0 | 622 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0009 | 0/0 | 284 | 6 | 0 | 3 | 2 | 0 | 1 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(279): Show |
chr16 | 755734 | 773862 |
a0010 | 0/0 | 622 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0011 | 0/0 | 622 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0012 | 0/0 | 622 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0013 | 0/0 | 622 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0014 | 0/0 | 622 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0015 | 0/0 | 622 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0016 | 0/0 | 622 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0017 | 0/0 | 622 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0018 | 0/0 | 622 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0019 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0020 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0021 | 0/0 | 165 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(160): Show |
chr16 | 755734 | 773862 |
a0022 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0023 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0024 | 0/0 | 622 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0025 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0026 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0027 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
a0028 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(279): Show |
chr16 | 755734 | 773862 |
a0029 | 0/0 | 284 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | MALPT others(279): Show |
chr16 | 755734 | 773862 |
a0030 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | MALPT others(617): Show |
chr16 | 755734 | 773862 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1866 | 149 | 21 | 29 | 77 | 7 | 14 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0001c0009 | 0/0 | 1866 | 7 | 0 | 0 | 7 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0001c0021 | 0/0 | 1866 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0001c0034 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0001c0037 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0001c0039 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0002c0002 | 0/1 | 1866 | 66 | 5 | 9 | 43 | 2 | 6 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0002c0003 | 0/0 | 1866 | 26 | 12 | 10 | 2 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0002c0015 | 0/0 | 1866 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0002c0024 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0002c0033 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0003c0004 | 0/0 | 1866 | 23 | 14 | 2 | 3 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0004c0006 | 0/0 | 1866 | 12 | 0 | 1 | 5 | 0 | 6 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0004c0016 | 0/0 | 1866 | 3 | 0 | 0 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0004c0020 | 0/0 | 1866 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0005c0005 | 0/0 | 1866 | 16 | 2 | 3 | 4 | 0 | 7 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0005c0043 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0006c0008 | 0/0 | 1866 | 8 | 6 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0006c0011 | 0/0 | 1866 | 6 | 5 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0007c0007 | 0/0 | 1866 | 9 | 9 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0008c0010 | 0/0 | 1866 | 7 | 7 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0009c0012 | 0/0 | 1867 | 5 | 0 | 3 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1862): Show |
chr16 | 755734 | 773862 | ||
a0009c0030 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1862): Show |
chr16 | 755734 | 773862 | ||
a0010c0014 | 0/0 | 1866 | 4 | 0 | 3 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0011c0013 | 0/0 | 1866 | 4 | 3 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0012c0017 | 0/0 | 1866 | 3 | 0 | 3 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0013c0018 | 0/0 | 1866 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0014c0023 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0014c0045 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0015c0022 | 0/0 | 1866 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0016c0027 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0016c0028 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0017c0019 | 0/0 | 1866 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0018c0046 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0019c0044 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0020c0038 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0021c0025 | 0/0 | 1832 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1827): Show |
chr16 | 755734 | 773862 | ||
a0022c0036 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0023c0040 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0024c0029 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0025c0035 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0026c0041 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0027c0032 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 | ||
a0028c0026 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1862): Show |
chr16 | 755734 | 773862 | ||
a0029c0042 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1862): Show |
chr16 | 755734 | 773862 | ||
a0030c0031 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | ATGGC others(1861): Show |
chr16 | 755734 | 773862 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2197 | 145 | 21 | 27 | 75 | 7 | 14 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0001t0005 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0001t0008 | 0/0 | 2171 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2166): Show |
chr16 | 755734 | 773862 |
a0001c0001t0010 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0001t0011 | 0/0 | 2207 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2202): Show |
chr16 | 755734 | 773862 |
a0001c0009t0001 | 0/0 | 2197 | 7 | 0 | 0 | 7 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0021t0001 | 0/0 | 2197 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0034t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0037t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0001c0039t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0002t0002 | 0/1 | 2197 | 65 | 5 | 8 | 43 | 2 | 6 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0002t0012 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0003t0001 | 0/0 | 2197 | 4 | 0 | 1 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0003t0002 | 0/0 | 2197 | 7 | 4 | 2 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0003t0004 | 0/0 | 2197 | 15 | 8 | 7 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0015t0003 | 0/0 | 2197 | 4 | 4 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0024t0002 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0002c0033t0003 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0003c0004t0003 | 0/0 | 2197 | 23 | 14 | 2 | 3 | 1 | 3 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0004c0006t0001 | 0/0 | 2197 | 12 | 0 | 1 | 5 | 0 | 6 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0004c0016t0001 | 0/0 | 2197 | 3 | 0 | 0 | 2 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0004c0020t0001 | 0/0 | 2197 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0005c0005t0001 | 0/0 | 2197 | 15 | 1 | 3 | 4 | 0 | 7 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0005c0005t0009 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0005c0043t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0006c0008t0001 | 0/0 | 2197 | 8 | 6 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0006c0011t0001 | 0/0 | 2197 | 6 | 5 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0007c0007t0001 | 0/0 | 2197 | 6 | 6 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0007c0007t0005 | 0/0 | 2197 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0008c0010t0002 | 0/0 | 2197 | 7 | 7 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0009c0012t0001 | 0/0 | 2198 | 5 | 0 | 3 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2193): Show |
chr16 | 755734 | 773862 |
a0009c0030t0002 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2193): Show |
chr16 | 755734 | 773862 |
a0010c0014t0001 | 0/0 | 2197 | 4 | 0 | 3 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0011c0013t0006 | 0/0 | 2196 | 2 | 1 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2191): Show |
chr16 | 755734 | 773862 |
a0011c0013t0007 | 0/0 | 2196 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2191): Show |
chr16 | 755734 | 773862 |
a0012c0017t0001 | 0/0 | 2197 | 3 | 0 | 3 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0013c0018t0001 | 0/0 | 2197 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0014c0023t0002 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0014c0023t0013 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0014c0045t0003 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0015c0022t0001 | 0/0 | 2197 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0016c0027t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0016c0028t0001 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0017c0019t0002 | 0/0 | 2197 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0018c0046t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0019c0044t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0020c0038t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0021c0025t0001 | 0/0 | 2163 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2158): Show |
chr16 | 755734 | 773862 |
a0022c0036t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0023c0040t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0024c0029t0001 | 0/0 | 2197 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0025c0035t0001 | 0/0 | 2197 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0026c0041t0001 | 0/0 | 2197 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0027c0032t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
a0028c0026t0003 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2193): Show |
chr16 | 755734 | 773862 |
a0029c0042t0002 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2193): Show |
chr16 | 755734 | 773862 |
a0030c0031t0001 | 0/0 | 2197 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | GTCAT others(2192): Show |
chr16 | 755734 | 773862 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0009t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0021t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0021t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0034t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0037t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0001c0039t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0295 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0002t0012g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0003t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0015t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0024t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0002c0033t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0002 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0003c0004t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0006t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0016t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0016t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0016t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0020t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0004c0020t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0005t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0005c0043t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0008t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0011t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0011t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0011t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0006c0011t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0007c0007t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0008c0010t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0012t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0012t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0012t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0012t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0012t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0009c0030t0002g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0014t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0010c0014t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0011c0013t0006g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0011c0013t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0011c0013t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0017t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0017t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0012c0017t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0013c0018t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0023t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0023t0013g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0014c0045t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0015c0022t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0015c0022t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0016c0027t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0016c0028t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0017c0019t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0017c0019t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0018c0046t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0019c0044t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0020c0038t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0021c0025t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0022c0036t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0023c0040t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0024c0029t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0025c0035t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0026c0041t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0027c0032t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0028c0026t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0029c0042t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
a0030c0031t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0027 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00140 | hp2 | a0018 | c0046 | t0001 | g0143 | EUR | GBR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | FIN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00423 | hp2 | a0003 | c0004 | t0003 | g0263 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00558 | hp1 | a0004 | c0020 | t0001 | g0287 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00609 | hp2 | a0019 | c0044 | t0001 | g0043 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0329 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00639 | hp1 | a0003 | c0004 | t0003 | g0003 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00639 | hp2 | a0005 | c0005 | t0001 | g0045 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00642 | hp1 | a0004 | c0006 | t0001 | g0261 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0304 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0079 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00735 | hp2 | a0002 | c0003 | t0001 | g0156 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00738 | hp2 | a0005 | c0005 | t0001 | g0040 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00741 | hp1 | a0010 | c0014 | t0001 | g0006 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01069 | hp2 | a0006 | c0008 | t0001 | g0023 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01071 | hp1 | a0006 | c0008 | t0001 | g0023 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01074 | hp1 | a0005 | c0005 | t0001 | g0196 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01081 | hp2 | a0010 | c0014 | t0001 | g0006 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01099 | hp1 | a0015 | c0022 | t0001 | g0029 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01099 | hp2 | a0020 | c0038 | t0001 | g0276 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01106 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01109 | hp2 | a0009 | c0012 | t0001 | g0008 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01169 | hp2 | a0010 | c0014 | t0001 | g0102 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01175 | hp1 | a0021 | c0025 | t0001 | g0167 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01175 | hp2 | a0009 | c0012 | t0001 | g0182 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0314 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0144 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01243 | hp2 | a0011 | c0013 | t0006 | g0019 | AMR | PUR | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0313 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01256 | hp2 | a0012 | c0017 | t0001 | g0082 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0296 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01361 | hp1 | a0001 | c0021 | t0001 | g0264 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01496 | hp1 | a0022 | c0036 | t0001 | g0126 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01496 | hp2 | a0023 | c0040 | t0001 | g0168 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0303 | EUR | IBS | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01884 | hp1 | a0016 | c0028 | t0001 | g0221 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01884 | hp2 | a0003 | c0004 | t0003 | g0028 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01891 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01891 | hp2 | a0008 | c0010 | t0002 | g0013 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01934 | hp2 | a0002 | c0003 | t0002 | g0254 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01943 | hp1 | a0024 | c0029 | t0001 | g0129 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01943 | hp2 | a0002 | c0003 | t0004 | g0209 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01952 | hp2 | a0002 | c0003 | t0004 | g0212 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01975 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01978 | hp1 | a0002 | c0003 | t0004 | g0210 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0320 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01981 | hp1 | a0006 | c0011 | t0001 | g0233 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01993 | hp2 | a0012 | c0017 | t0001 | g0083 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02004 | hp1 | a0002 | c0003 | t0004 | g0216 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02004 | hp2 | a0002 | c0002 | t0012 | g0027 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02015 | hp1 | a0009 | c0012 | t0001 | g0132 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02027 | hp1 | a0001 | c0001 | t0010 | g0137 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02040 | hp1 | a0001 | c0009 | t0001 | g0292 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02055 | hp1 | a0007 | c0007 | t0001 | g0007 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02055 | hp2 | a0008 | c0010 | t0002 | g0054 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02056 | hp2 | a0002 | c0003 | t0001 | g0089 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02071 | hp2 | a0004 | c0006 | t0001 | g0255 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0283 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02080 | hp2 | a0004 | c0006 | t0001 | g0260 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0271 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02129 | hp1 | a0001 | c0037 | t0001 | g0087 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0316 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02155 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02155 | hp2 | a0017 | c0019 | t0002 | g0286 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | CDX | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02257 | hp2 | a0011 | c0013 | t0007 | g0205 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02258 | hp1 | a0003 | c0004 | t0003 | g0267 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02258 | hp2 | a0006 | c0011 | t0001 | g0232 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02273 | hp1 | a0002 | c0003 | t0004 | g0213 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02280 | hp2 | a0007 | c0007 | t0001 | g0052 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02293 | hp2 | a0002 | c0003 | t0004 | g0211 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02300 | hp2 | a0002 | c0003 | t0004 | g0208 | AMR | PEL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02451 | hp1 | a0013 | c0018 | t0001 | g0009 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02451 | hp2 | a0006 | c0008 | t0001 | g0032 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02523 | hp2 | a0017 | c0019 | t0002 | g0285 | EAS | KHV | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02572 | hp1 | a0011 | c0013 | t0007 | g0206 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02572 | hp2 | a0013 | c0018 | t0001 | g0009 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02602 | hp1 | a0004 | c0006 | t0001 | g0331 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02615 | hp1 | a0006 | c0008 | t0001 | g0252 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02615 | hp2 | a0006 | c0011 | t0001 | g0230 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02622 | hp2 | a0014 | c0023 | t0002 | g0037 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02630 | hp1 | a0008 | c0010 | t0002 | g0013 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02630 | hp2 | a0008 | c0010 | t0002 | g0038 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0241 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02647 | hp2 | a0002 | c0003 | t0004 | g0226 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02683 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02717 | hp2 | a0007 | c0007 | t0005 | g0225 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02723 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02735 | hp1 | a0003 | c0004 | t0003 | g0268 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0192 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02809 | hp1 | a0007 | c0007 | t0001 | g0007 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02818 | hp1 | a0002 | c0003 | t0004 | g0228 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02818 | hp2 | a0003 | c0004 | t0003 | g0223 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02886 | hp1 | a0002 | c0003 | t0002 | g0242 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02895 | hp1 | a0003 | c0004 | t0003 | g0337 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02965 | hp1 | a0008 | c0010 | t0002 | g0053 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02965 | hp2 | a0002 | c0003 | t0004 | g0021 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02970 | hp1 | a0007 | c0007 | t0005 | g0020 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02970 | hp2 | a0006 | c0011 | t0001 | g0022 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02976 | hp1 | a0002 | c0003 | t0004 | g0214 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02976 | hp2 | a0003 | c0004 | t0003 | g0028 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03017 | hp2 | a0001 | c0034 | t0001 | g0204 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03041 | hp2 | a0007 | c0007 | t0005 | g0020 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0301 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03098 | hp2 | a0007 | c0007 | t0001 | g0239 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03130 | hp2 | a0002 | c0003 | t0004 | g0227 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03139 | hp1 | a0006 | c0008 | t0001 | g0224 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03139 | hp2 | a0011 | c0013 | t0006 | g0019 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03195 | hp2 | a0005 | c0005 | t0001 | g0047 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03209 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03209 | hp2 | a0008 | c0010 | t0002 | g0251 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03225 | hp2 | a0002 | c0003 | t0002 | g0247 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03239 | hp1 | a0005 | c0005 | t0001 | g0044 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0099 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03453 | hp1 | a0003 | c0004 | t0003 | g0003 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03486 | hp1 | a0005 | c0005 | t0009 | g0041 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03486 | hp2 | a0002 | c0033 | t0003 | g0253 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03490 | hp2 | a0005 | c0005 | t0001 | g0012 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03492 | hp2 | a0005 | c0005 | t0001 | g0012 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03516 | hp1 | a0002 | c0003 | t0004 | g0215 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03540 | hp1 | a0007 | c0007 | t0001 | g0007 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03540 | hp2 | a0007 | c0007 | t0001 | g0240 | AFR | GWD | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03579 | hp1 | a0002 | c0015 | t0003 | g0250 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03579 | hp2 | a0006 | c0008 | t0001 | g0248 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0262 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03654 | hp2 | a0005 | c0005 | t0001 | g0050 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03669 | hp1 | a0001 | c0021 | t0001 | g0175 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03669 | hp2 | a0005 | c0005 | t0001 | g0031 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03688 | hp1 | a0003 | c0004 | t0003 | g0269 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03688 | hp2 | a0005 | c0005 | t0001 | g0036 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0312 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03704 | hp2 | a0002 | c0024 | t0002 | g0282 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03710 | hp1 | a0003 | c0004 | t0003 | g0265 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03710 | hp2 | a0025 | c0035 | t0001 | g0181 | SAS | PJL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03834 | hp1 | a0004 | c0016 | t0001 | g0257 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03927 | hp1 | a0004 | c0006 | t0001 | g0220 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0310 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04115 | hp1 | a0004 | c0006 | t0001 | g0179 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04184 | hp1 | a0009 | c0030 | t0002 | g0338 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04184 | hp2 | a0005 | c0043 | t0001 | g0049 | SAS | BEB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0278 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0318 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04204 | hp1 | a0004 | c0006 | t0001 | g0245 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04204 | hp2 | a0004 | c0006 | t0001 | g0234 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04228 | hp1 | a0004 | c0006 | t0001 | g0335 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18522 | hp1 | a0002 | c0003 | t0002 | g0243 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18522 | hp2 | a0002 | c0003 | t0004 | g0021 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0298 | EAS | CHB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18906 | hp1 | a0026 | c0041 | t0001 | g0011 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18906 | hp2 | a0002 | c0015 | t0003 | g0071 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18939 | hp1 | a0001 | c0009 | t0001 | g0024 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0307 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18946 | hp2 | a0001 | c0009 | t0001 | g0024 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18949 | hp2 | a0004 | c0016 | t0001 | g0258 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18950 | hp1 | a0027 | c0032 | t0001 | g0327 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18950 | hp2 | a0001 | c0009 | t0001 | g0289 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18959 | hp1 | a0005 | c0005 | t0001 | g0046 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0200 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18969 | hp1 | a0004 | c0016 | t0001 | g0139 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18969 | hp2 | a0004 | c0006 | t0001 | g0259 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18980 | hp1 | a0005 | c0005 | t0001 | g0048 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18995 | hp2 | a0005 | c0005 | t0001 | g0042 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18999 | hp1 | a0001 | c0009 | t0001 | g0293 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19007 | hp1 | a0001 | c0009 | t0001 | g0290 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19012 | hp1 | a0014 | c0045 | t0003 | g0039 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19030 | hp1 | a0028 | c0026 | t0003 | g0002 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19030 | hp2 | a0029 | c0042 | t0002 | g0244 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19043 | hp2 | a0006 | c0008 | t0001 | g0011 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19055 | hp1 | a0004 | c0020 | t0001 | g0330 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19057 | hp1 | a0004 | c0006 | t0001 | g0183 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19063 | hp2 | a0030 | c0031 | t0001 | g0176 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19066 | hp2 | a0001 | c0039 | t0001 | g0147 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19079 | hp1 | a0001 | c0009 | t0001 | g0291 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19083 | hp1 | a0004 | c0006 | t0001 | g0256 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19083 | hp2 | a0009 | c0012 | t0001 | g0325 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19084 | hp2 | a0003 | c0004 | t0003 | g0270 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19088 | hp2 | a0016 | c0027 | t0001 | g0185 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19089 | hp1 | a0005 | c0005 | t0001 | g0034 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19240 | hp1 | a0006 | c0011 | t0001 | g0022 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA19240 | hp2 | a0002 | c0002 | t0002 | g0284 | AFR | YRI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20129 | hp1 | a0003 | c0004 | t0003 | g0266 | AFR | ASW | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20129 | hp2 | a0002 | c0015 | t0003 | g0172 | AFR | ASW | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20752 | hp2 | a0010 | c0014 | t0001 | g0006 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20805 | hp2 | a0003 | c0004 | t0003 | g0002 | EUR | TSI | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20905 | hp1 | a0005 | c0005 | t0001 | g0033 | SAS | GIH | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20905 | hp2 | a0015 | c0022 | t0001 | g0030 | SAS | GIH | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01123 | hp1 | a0012 | c0017 | t0001 | g0184 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG01123 | hp2 | a0009 | c0012 | t0001 | g0201 | AMR | CLM | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02109 | hp1 | a0002 | c0015 | t0003 | g0249 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02109 | hp2 | a0003 | c0004 | t0003 | g0002 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02486 | hp1 | a0006 | c0011 | t0001 | g0231 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02486 | hp2 | a0003 | c0004 | t0003 | g0280 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02559 | hp1 | a0008 | c0010 | t0002 | g0055 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG02559 | hp2 | a0003 | c0004 | t0003 | g0002 | AFR | ACB | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03471 | hp1 | a0013 | c0018 | t0001 | g0009 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG06807 | hp1 | a0006 | c0008 | t0001 | g0035 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA20300 | hp2 | a0014 | c0023 | t0013 | g0279 | AFR | USA | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA21309 | hp1 | a0002 | c0003 | t0004 | g0207 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
NA21309 | hp2 | a0003 | c0004 | t0003 | g0222 | AFR | LWK | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0295 | REF | REF | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0058 | REF | REF | MSLN_chr16_755734_773862 | MSLN | chr16 | 755734 | 773862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:763260 | C | T | 1 | a0018 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.113C>T | p.Ala38Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/18 | 312/2197 | 113/1869 | 38/622 | chr16 | 763260 | |||
chr16:764058 | C | T | 5 | a0005 a0008 a0014 others(2): Show |
29 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(26): Show |
missense_variant | MODERATE | c.215C>T | p.Ala72Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/18 | 414/2197 | 215/1869 | 72/622 | chr16 | 764058 | |||
chr16:764091 | G | A | 1 | a0017 | 2 | HG02155.hp2 HG02523.hp2 |
missense_variant | MODERATE | c.248G>A | p.Arg83Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/18 | 447/2197 | 248/1869 | 83/622 | chr16 | 764091 | |||
chr16:764648 | TGCGCTGT others(27): Show |
T | 1 | a0021 | 1 | HG01175.hp1 | frameshift_variant | HIGH | c.304_337delCGCTGTCT others(26): Show |
p.Cys103fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 503/2197 | 304/1869 | 102/622 | INFO_REALIGN_3_PRIME | chr16 | 764648 | ||
chr16:764698 | C | G | 1 | a0013 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.352C>G | p.Leu118Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 551/2197 | 352/1869 | 118/622 | chr16 | 764698 | |||
chr16:764942 | G | A | 4 | a0003 a0013 a0016 others(1): Show |
29 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(26): Show |
missense_variant | MODERATE | c.416G>A | p.Arg139His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 8/18 | 615/2197 | 416/1869 | 139/622 | chr16 | 764942 | |||
chr16:765110 | G | A | 1 | a0024 | 1 | HG01943.hp1 | missense_variant&splice_region_variant | MODERATE | c.511G>A | p.Gly171Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 710/2197 | 511/1869 | 171/622 | chr16 | 765110 | |||
chr16:765214 | A | AC | 3 | a0009 a0028 a0029 |
8 | HG01109.hp2 HG01123.hp2 HG01175.hp2 others(5): Show |
frameshift_variant | HIGH | c.619dupC | p.Arg207fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 819/2197 | 620/1869 | 207/622 | INFO_REALIGN_3_PRIME | chr16 | 765214 | ||
chr16:765549 | T | C | 3 | a0004 a0027 a0030 |
19 | HG00558.hp1 HG00642.hp1 HG02071.hp2 others(16): Show |
missense_variant | MODERATE | c.727T>C | p.Ser243Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 926/2197 | 727/1869 | 243/622 | chr16 | 765549 | |||
chr16:765565 | T | C | 3 | a0004 a0027 a0030 |
19 | HG00558.hp1 HG00642.hp1 HG02071.hp2 others(16): Show |
missense_variant | MODERATE | c.743T>C | p.Leu248Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 942/2197 | 743/1869 | 248/622 | chr16 | 765565 | |||
chr16:765593 | G | C | 2 | a0008 a0029 |
8 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.771G>C | p.Gln257His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/18 | 970/2197 | 771/1869 | 257/622 | chr16 | 765593 | |||
chr16:765692 | G | A | 1 | a0030 | 1 | NA19063.hp2 | missense_variant&splice_region_variant | MODERATE | c.797G>A | p.Gly266Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/18 | 996/2197 | 797/1869 | 266/622 | chr16 | 765692 | |||
chr16:766089 | G | A | 1 | a0011 | 4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
missense_variant | MODERATE | c.926G>A | p.Arg309His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1125/2197 | 926/1869 | 309/622 | chr16 | 766089 | |||
chr16:766091 | G | A | 2 | a0027 a0030 |
2 | NA18950.hp1 NA19063.hp2 |
missense_variant | MODERATE | c.928G>A | p.Glu310Lys | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1127/2197 | 928/1869 | 310/622 | chr16 | 766091 | |||
chr16:766149 | C | T | 1 | a0012 | 3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
missense_variant | MODERATE | c.986C>T | p.Ala329Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1185/2197 | 986/1869 | 329/622 | chr16 | 766149 | |||
chr16:766464 | A | G | 2 | a0006 a0026 |
15 | HG01069.hp2 HG01071.hp1 HG01981.hp1 others(12): Show |
missense_variant | MODERATE | c.1204A>G | p.Asn402Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/18 | 1403/2197 | 1204/1869 | 402/622 | chr16 | 766464 | |||
chr16:766973 | A | G | 2 | a0007 a0013 |
12 | HG02055.hp1 HG02280.hp2 HG02451.hp1 others(9): Show |
missense_variant | MODERATE | c.1462A>G | p.Asn488Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/18 | 1661/2197 | 1462/1869 | 488/622 | chr16 | 766973 | |||
chr16:766977 | G | A | 3 | a0010 a0018 a0021 |
6 | HG00140.hp2 HG00741.hp1 HG01081.hp2 others(3): Show |
missense_variant | MODERATE | c.1466G>A | p.Gly489Glu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/18 | 1665/2197 | 1466/1869 | 489/622 | chr16 | 766977 | |||
chr16:768446 | G | A | 1 | a0025 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1664G>A | p.Arg555Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1863/2197 | 1664/1869 | 555/622 | chr16 | 768446 | |||
chr16:768452 | G | A | 1 | a0015 | 2 | HG01099.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.1670G>A | p.Arg557His | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1869/2197 | 1670/1869 | 557/622 | chr16 | 768452 | |||
chr16:768482 | G | A | 1 | a0022 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1700G>A | p.Arg567Gln | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1899/2197 | 1700/1869 | 567/622 | chr16 | 768482 | |||
chr16:768533 | A | G | 1 | a0023 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1751A>G | p.Asn584Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1950/2197 | 1751/1869 | 584/622 | chr16 | 768533 | |||
chr16:768559 | A | G | 11 | a0002 a0003 a0007 others(8): Show |
151 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(148): Show |
missense_variant | MODERATE | c.1777A>G | p.Met593Val | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1976/2197 | 1777/1869 | 593/622 | chr16 | 768559 | |||
chr16:768687 | C | T | 1 | a0020 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.1823C>T | p.Pro608Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2022/2197 | 1823/1869 | 608/622 | chr16 | 768687 | |||
chr16:768728 | G | C | 1 | a0019 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1864G>C | p.Ala622Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2063/2197 | 1864/1869 | 622/622 | chr16 | 768728 | |||
chr16:768731 | T | A | 1 | a0001 | 1 | HG01192.hp2 | stop_lost | HIGH | c.1867T>A | p.Ter623Argext*? | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2066/2197 | 1867/1869 | 623/622 | chr16 | 768731 | |||
chr16:768732 | GAGGGCCC others(19): Show |
G | 1 | a0001 | 1 | HG01192.hp2 | frameshift_variant&stop_lost | HIGH | c.1869_*25delAGGGCCC others(19): Show |
p.Ter623fs | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 2068/2197 | 1869/1869 | 623/622 | chr16 | 768732 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:763650 | G | A | 5 | a0001c0009 a0002c0002 a0002c0024 others(2): Show |
77 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(74): Show |
synonymous_variant | LOW | c.138G>A | p.Ala46Ala | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/18 | 337/2197 | 138/1869 | 46/622 | chr16 | 763650 | |||
chr16:764649 | G | T | 1 | a0007c0007 | 4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.303G>T | p.Leu101Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/18 | 502/2197 | 303/1869 | 101/622 | chr16 | 764649 | |||
chr16:765202 | C | T | 1 | a0006c0011 | 6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.603C>T | p.Ala201Ala | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/18 | 802/2197 | 603/1869 | 201/622 | chr16 | 765202 | |||
chr16:766072 | T | C | 9 | a0001c0021 a0002c0033 a0004c0006 others(6): Show |
24 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(21): Show |
synonymous_variant | LOW | c.909T>C | p.Pro303Pro | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1108/2197 | 909/1869 | 303/622 | chr16 | 766072 | |||
chr16:766099 | C | T | 1 | a0002c0033 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.936C>T | p.Asp312Asp | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/18 | 1135/2197 | 936/1869 | 312/622 | chr16 | 766099 | |||
chr16:766406 | G | A | 1 | a0001c0034 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1146G>A | p.Glu382Glu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/18 | 1345/2197 | 1146/1869 | 382/622 | chr16 | 766406 | |||
chr16:767407 | C | T | 6 | a0002c0015 a0002c0033 a0003c0004 others(3): Show |
34 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(31): Show |
synonymous_variant | LOW | c.1533C>T | p.Leu511Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/18 | 1732/2197 | 1533/1869 | 511/622 | chr16 | 767407 | |||
chr16:767458 | G | A | 1 | a0002c0024 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1584G>A | p.Thr528Thr | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/18 | 1783/2197 | 1584/1869 | 528/622 | chr16 | 767458 | |||
chr16:768555 | C | T | 8 | a0001c0021 a0001c0039 a0004c0006 others(5): Show |
21 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(18): Show |
synonymous_variant | LOW | c.1773C>T | p.Leu591Leu | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/18 | 1972/2197 | 1773/1869 | 591/622 | chr16 | 768555 | |||
chr16:768658 | G | A | 1 | a0001c0037 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.1794G>A | p.Ser598Ser | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 1993/2197 | 1794/1869 | 598/622 | chr16 | 768658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:760757 | C | T | 3 | a0001c0001t0005 a0002c0003t0004 a0007c0007t0005 |
19 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | chr16 | 760757 | |||||||
chr16:760758 | G | A | 1 | a0011c0013t0006 | 2 | HG01243.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-175G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | 1923 | chr16 | 760758 | ||||||
chr16:760783 | C | T | 1 | a0014c0023t0013 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-150C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/18 | 1898 | chr16 | 760783 | ||||||
chr16:761110 | C | T | 1 | a0002c0002t0012 | 1 | HG02004.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-74C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | chr16 | 761110 | |||||||
chr16:761113 | C | CTGCTGTG others(3): Show |
1 | a0001c0001t0011 | 1 | NA18959.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70_-61dupTGCTGTGA others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | 1557 | INFO_REALIGN_3_PRIME | chr16 | 761113 | |||||
chr16:761166 | C | G | 1 | a0001c0001t0010 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/18 | 1515 | chr16 | 761166 | ||||||
chr16:768759 | G | C | 1 | a0001c0001t0008 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 26 | chr16 | 768759 | ||||||
chr16:768797 | G | A | 1 | a0005c0005t0009 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 64 | chr16 | 768797 | ||||||
chr16:768802 | G | A | 11 | a0002c0002t0002 a0002c0002t0012 a0002c0003t0002 others(8): Show |
101 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 69 | chr16 | 768802 | ||||||
chr16:768807 | C | T | 7 | a0002c0015t0003 a0002c0033t0003 a0003c0004t0003 others(4): Show |
34 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*74C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 74 | chr16 | 768807 | ||||||
chr16:768849 | GC | G | 2 | a0011c0013t0006 a0011c0013t0007 |
4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*121delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 18/18 | 121 | INFO_REALIGN_3_PRIME | chr16 | 768849 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:760844 | T | A | 2 | a0015c0022t0001g0029 a0015c0022t0001g0030 |
2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-112+23T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760844 | |||||||
chr16:760921 | C | T | 3 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0009c0030t0002g0338 |
3 | HG00140.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-112+100C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760921 | |||||||
chr16:760934 | G | A | 29 | a0001c0001t0001g0051 a0005c0005t0001g0012 a0005c0005t0001g0031 others(26): Show |
31 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-112+113G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760934 | |||||||
chr16:760947 | C | T | 2 | a0003c0004t0003g0028 a0003c0004t0003g0337 |
3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-112+126C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760947 | |||||||
chr16:760972 | G | C | 2 | a0015c0022t0001g0029 a0015c0022t0001g0030 |
2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-111-101G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760972 | |||||||
chr16:760975 | G | C | 1 | a0002c0002t0002g0056 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-111-98G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 760975 | |||||||
chr16:761029 | C | T | 1 | a0001c0001t0001g0336 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-111-44C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 1/17 | chr16 | 761029 | |||||||
chr16:761199 | C | T | 340 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(337): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.-10+25C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761199 | |||||||
chr16:761325 | C | T | 1 | a0004c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-10+151C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761325 | |||||||
chr16:761338 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-10+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761338 | |||||||
chr16:761347 | C | T | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-10+173C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761347 | |||||||
chr16:761348 | G | A | 1 | a0005c0005t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-10+174G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761348 | |||||||
chr16:761382 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-10+208C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761382 | |||||||
chr16:761410 | G | A | 1 | a0002c0002t0002g0060 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-10+236G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761410 | |||||||
chr16:761433 | A | G | 187 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0051 others(184): Show |
222 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.-10+259A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761433 | |||||||
chr16:761629 | TG | T | 154 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0051 others(151): Show |
185 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.-10+463delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 761629 | ||||||
chr16:761746 | C | T | 60 | a0001c0001t0001g0281 a0001c0001t0001g0324 a0001c0001t0001g0326 others(57): Show |
72 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.-10+572C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761746 | |||||||
chr16:761803 | G | A | 1 | a0005c0005t0001g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10+629G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761803 | |||||||
chr16:761904 | C | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-10+730C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761904 | |||||||
chr16:761938 | C | G | 4 | a0008c0010t0002g0013 a0008c0010t0002g0053 a0008c0010t0002g0054 others(1): Show |
5 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-734C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761938 | |||||||
chr16:761946 | C | G | 43 | a0001c0001t0001g0051 a0001c0001t0001g0197 a0001c0001t0001g0198 others(40): Show |
47 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.-9-726C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 761946 | |||||||
chr16:762008 | C | A | 35 | a0001c0001t0001g0051 a0002c0002t0002g0278 a0005c0005t0001g0012 others(32): Show |
38 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-9-664C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762008 | |||||||
chr16:762030 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-9-642G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762030 | |||||||
chr16:762273 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0051 others(193): Show |
231 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(228): Show |
intron_variant | MODIFIER | c.-9-399A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762273 | |||||||
chr16:762274 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-9-398A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762274 | |||||||
chr16:762306 | T | C | 1 | a0002c0024t0002g0282 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-9-366T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762306 | |||||||
chr16:762539 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0272 a0001c0001t0001g0273 others(23): Show |
39 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.-9-133C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | chr16 | 762539 | |||||||
chr16:762638 | A | AG | 6 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0002c0002t0002g0186 others(3): Show |
6 | HG02080.hp1 HG02155.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-29dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr16 | 762638 | ||||||
chr16:762848 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.85+83C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 762848 | |||||||
chr16:762889 | G | C | 1 | a0006c0011t0001g0230 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.85+124G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 762889 | |||||||
chr16:763120 | T | C | 3 | a0011c0013t0006g0019 a0011c0013t0007g0205 a0011c0013t0007g0206 |
4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-113T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 763120 | |||||||
chr16:763165 | C | T | 1 | a0012c0017t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.86-68C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 3/17 | chr16 | 763165 | |||||||
chr16:763307 | G | T | 1 | a0011c0013t0006g0019 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.129+31G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763307 | |||||||
chr16:763327 | G | A | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+51G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763327 | |||||||
chr16:763339 | T | C | 1 | a0002c0002t0002g0284 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+63T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763339 | |||||||
chr16:763388 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(2): Show |
5 | HG00423.hp1 HG02056.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+112G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763388 | |||||||
chr16:763602 | A | T | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.130-40A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 4/17 | chr16 | 763602 | |||||||
chr16:763742 | G | T | 1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.179+51G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763742 | |||||||
chr16:763764 | C | CCCATCCC others(128): Show |
1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+75_179+76insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763764 | ||||||
chr16:763768 | A | ATCCCCCA others(126): Show |
3 | a0008c0010t0002g0013 a0008c0010t0002g0053 a0008c0010t0002g0054 |
4 | HG01891.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763768 | ||||||
chr16:763768 | A | C | 1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+77A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763768 | |||||||
chr16:763775 | A | AGCATCCC others(142): Show |
1 | a0002c0003t0004g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
1 | a0004c0006t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(115): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02717.hp1 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(127): Show |
1 | a0002c0002t0002g0229 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
56 | a0001c0001t0001g0070 a0001c0009t0001g0024 a0001c0009t0001g0289 others(53): Show |
68 | HG00099.hp2 HG00558.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
46 | a0001c0001t0001g0004 a0001c0001t0001g0062 a0001c0001t0001g0072 others(43): Show |
62 | HG00639.hp1 HG01099.hp1 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0077 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(124): Show |
1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(129): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(127): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
1 | a0002c0002t0002g0192 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
178 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(175): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(141): Show |
16 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0005g0217 others(13): Show |
17 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(125): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
15 | a0001c0021t0001g0264 a0002c0003t0002g0254 a0002c0003t0002g0262 others(12): Show |
15 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(128): Show |
1 | a0011c0013t0007g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(127): Show |
1 | a0001c0001t0001g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(162): Show |
1 | a0001c0001t0001g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(167): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(83): Show |
1 | a0001c0001t0001g0332 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
2 | a0002c0002t0002g0194 a0002c0002t0002g0195 |
2 | NA19003.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(126): Show |
1 | a0025c0035t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(128): Show |
1 | a0009c0012t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | AGCATCCC others(125): Show |
3 | a0007c0007t0001g0052 a0007c0007t0005g0020 a0007c0007t0005g0225 |
4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763775 | ||||||
chr16:763775 | A | C | 1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.179+84A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763775 | |||||||
chr16:763776 | G | GCATCCCA others(126): Show |
1 | a0012c0017t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.179+91_179+92insAT others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763776 | ||||||
chr16:763780 | C | CCCATCCC others(125): Show |
1 | a0002c0002t0002g0323 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.179+91_179+92insAT others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr16 | 763780 | ||||||
chr16:763783 | C | A | 3 | a0008c0010t0002g0013 a0008c0010t0002g0053 a0008c0010t0002g0054 |
4 | HG01891.hp2 HG02055.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+92C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763783 | |||||||
chr16:763891 | G | A | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.180-132G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763891 | |||||||
chr16:763900 | G | C | 15 | a0001c0001t0005g0217 a0002c0003t0004g0021 a0002c0003t0004g0207 others(12): Show |
16 | HG01943.hp2 HG01952.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.180-123G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763900 | |||||||
chr16:763917 | C | T | 1 | a0020c0038t0001g0276 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.180-106C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763917 | |||||||
chr16:763955 | T | C | 17 | a0001c0021t0001g0264 a0002c0003t0002g0254 a0002c0003t0002g0262 others(14): Show |
17 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.180-68T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763955 | |||||||
chr16:763975 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-48T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763975 | |||||||
chr16:763977 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-46G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763977 | |||||||
chr16:763978 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-45C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763978 | |||||||
chr16:763980 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-43G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763980 | |||||||
chr16:763981 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-42G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763981 | |||||||
chr16:763983 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-40G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763983 | |||||||
chr16:763984 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-39A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763984 | |||||||
chr16:763985 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-38G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763985 | |||||||
chr16:763987 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-36G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763987 | |||||||
chr16:763988 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.180-35G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 5/17 | chr16 | 763988 | |||||||
chr16:764243 | C | T | 17 | a0001c0021t0001g0264 a0002c0003t0002g0254 a0002c0003t0002g0262 others(14): Show |
17 | HG00423.hp2 HG00642.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.300+100C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764243 | |||||||
chr16:764275 | C | T | 9 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(6): Show |
10 | HG01099.hp1 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+132C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764275 | |||||||
chr16:764295 | A | G | 103 | a0001c0001t0001g0075 a0001c0001t0001g0235 a0001c0001t0001g0236 others(100): Show |
120 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.300+152A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764295 | |||||||
chr16:764307 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0219 others(74): Show |
92 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.300+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764307 | |||||||
chr16:764354 | T | A | 66 | a0001c0009t0001g0024 a0001c0009t0001g0289 a0001c0009t0001g0290 others(63): Show |
78 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.300+211T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764354 | |||||||
chr16:764374 | C | A | 1 | a0002c0024t0002g0282 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300+231C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764374 | |||||||
chr16:764494 | A | G | 131 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(128): Show |
150 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.301-153A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764494 | |||||||
chr16:764524 | C | T | 8 | a0001c0001t0001g0008 a0002c0003t0002g0241 a0002c0003t0002g0242 others(5): Show |
9 | HG01109.hp2 HG02109.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.301-123C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764524 | |||||||
chr16:764607 | C | T | 1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.301-40C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764607 | |||||||
chr16:764617 | C | T | 3 | a0001c0021t0001g0264 a0015c0022t0001g0029 a0015c0022t0001g0030 |
3 | HG01099.hp1 HG01361.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.301-30C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 6/17 | chr16 | 764617 | |||||||
chr16:764742 | T | A | 1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.380+16T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764742 | |||||||
chr16:764749 | AC | A | 29 | a0001c0001t0001g0177 a0002c0015t0003g0249 a0002c0015t0003g0250 others(26): Show |
31 | HG00609.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.380+30delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr16 | 764749 | ||||||
chr16:764754 | C | T | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.380+28C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764754 | |||||||
chr16:764756 | C | A | 3 | a0007c0007t0001g0052 a0007c0007t0005g0020 a0007c0007t0005g0225 |
4 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+30C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 7/17 | chr16 | 764756 | |||||||
chr16:765100 | C | G | 1 | a0002c0033t0003g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.511-10C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 8/17 | chr16 | 765100 | |||||||
chr16:765350 | T | C | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.704+47T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765350 | |||||||
chr16:765370 | T | C | 177 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0219 others(174): Show |
208 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.704+67T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765370 | |||||||
chr16:765379 | T | C | 178 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0219 others(175): Show |
209 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.704+76T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765379 | |||||||
chr16:765411 | A | T | 1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.704+108A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765411 | |||||||
chr16:765413 | C | A | 107 | a0001c0001t0001g0008 a0001c0001t0001g0218 a0001c0001t0001g0219 others(104): Show |
126 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.704+110C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765413 | |||||||
chr16:765416 | C | T | 1 | a0006c0008t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.705-111C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 9/17 | chr16 | 765416 | |||||||
chr16:765628 | A | G | 340 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(337): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.795+11A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 10/17 | chr16 | 765628 | |||||||
chr16:765808 | C | T | 1 | a0002c0002t0002g0278 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.895+18C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 765808 | |||||||
chr16:765989 | A | T | 1 | a0006c0011t0001g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.896-70A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 765989 | |||||||
chr16:766012 | G | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.896-47G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766012 | |||||||
chr16:766020 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG00423.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.896-39C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766020 | |||||||
chr16:766032 | C | G | 2 | a0005c0005t0001g0036 a0005c0005t0001g0050 |
2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.896-27C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 11/17 | chr16 | 766032 | |||||||
chr16:766287 | C | T | 22 | a0001c0021t0001g0175 a0001c0021t0001g0264 a0004c0006t0001g0179 others(19): Show |
22 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1075-48C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766287 | |||||||
chr16:766294 | T | G | 175 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0218 others(172): Show |
206 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(203): Show |
intron_variant | MODIFIER | c.1075-41T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766294 | |||||||
chr16:766306 | A | G | 1 | a0002c0033t0003g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1075-29A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 12/17 | chr16 | 766306 | |||||||
chr16:766499 | C | T | 8 | a0002c0003t0002g0254 a0002c0003t0004g0208 a0002c0003t0004g0209 others(5): Show |
8 | HG01934.hp2 HG01943.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1230+9C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766499 | |||||||
chr16:766500 | C | T | 19 | a0002c0003t0002g0247 a0002c0015t0003g0071 a0003c0004t0003g0002 others(16): Show |
27 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1230+10C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766500 | |||||||
chr16:766506 | G | T | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+16G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766506 | |||||||
chr16:766550 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1230+60G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766550 | |||||||
chr16:766618 | A | C | 1 | a0006c0011t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1231-50A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 13/17 | chr16 | 766618 | |||||||
chr16:766847 | G | A | 1 | a0002c0002t0002g0288 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1373+37G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 14/17 | chr16 | 766847 | |||||||
chr16:766874 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1374-11C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 14/17 | chr16 | 766874 | |||||||
chr16:767016 | AGCCAGGG others(8): Show |
A | 109 | a0001c0001t0001g0246 a0002c0002t0002g0001 a0002c0002t0002g0010 others(106): Show |
130 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.1501+12_1501+26del others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr16 | 767016 | ||||||
chr16:767024 | A | T | 1 | a0009c0030t0002g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1501+12A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767024 | |||||||
chr16:767025 | GTCCCTGG others(7): Show |
G | 1 | a0009c0030t0002g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1501+14_1501+27del others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767025 | |||||||
chr16:767071 | C | A | 1 | a0002c0002t0002g0056 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1501+59C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767071 | |||||||
chr16:767176 | G | A | 2 | a0001c0021t0001g0264 a0004c0006t0001g0234 |
2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1501+164G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767176 | |||||||
chr16:767190 | C | T | 9 | a0008c0010t0002g0013 a0008c0010t0002g0038 a0008c0010t0002g0053 others(6): Show |
10 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1501+178C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767190 | |||||||
chr16:767213 | G | A | 103 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0218 others(100): Show |
122 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.1502-163G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767213 | |||||||
chr16:767237 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1502-139C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767237 | |||||||
chr16:767238 | G | C | 1 | a0001c0001t0001g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1502-138G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767238 | |||||||
chr16:767241 | T | C | 91 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0246 others(88): Show |
108 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(105): Show |
intron_variant | MODIFIER | c.1502-135T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767241 | |||||||
chr16:767262 | ATCCCTAA others(9): Show |
A | 1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1502-113_1502-98de others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767262 | |||||||
chr16:767339 | G | T | 87 | a0001c0001t0001g0246 a0002c0002t0002g0001 a0002c0002t0002g0010 others(84): Show |
104 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1502-37G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767339 | |||||||
chr16:767364 | C | G | 1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1502-12C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767364 | |||||||
chr16:767369 | C | T | 1 | a0002c0003t0004g0207 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.1502-7C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 15/17 | chr16 | 767369 | |||||||
chr16:767481 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1596+11C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767481 | |||||||
chr16:767484 | G | A | 4 | a0002c0003t0004g0207 a0011c0013t0006g0019 a0011c0013t0007g0205 others(1): Show |
5 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+14G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767484 | |||||||
chr16:767493 | C | T | 16 | a0001c0001t0001g0246 a0002c0003t0002g0254 a0002c0003t0004g0021 others(13): Show |
17 | HG00738.hp1 HG01934.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+23C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767493 | |||||||
chr16:767495 | T | TGTGGAGG others(39): Show |
1 | a0005c0005t0009g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+33_1596+78dup others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | ||||||
chr16:767495 | T | TGTGGAGG others(35): Show |
5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+32_1596+33ins others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | ||||||
chr16:767495 | T | TGTGGGGG others(34): Show |
1 | a0003c0004t0003g0266 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596+29_1596+30ins others(41): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | ||||||
chr16:767495 | T | TGTGGGGG others(35): Show |
1 | a0003c0004t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+29_1596+30ins others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767495 | ||||||
chr16:767502 | G | GGGGGGGC others(36): Show |
1 | a0003c0004t0003g0271 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1596+32_1596+33ins others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767502 | |||||||
chr16:767503 | A | G | 2 | a0003c0004t0003g0263 a0003c0004t0003g0271 |
2 | HG00423.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1596+33A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767503 | |||||||
chr16:767509 | C | CCGTGGAG others(24): Show |
2 | a0005c0005t0001g0034 a0005c0005t0001g0042 |
2 | NA18995.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+48_1596+78dup others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767509 | ||||||
chr16:767509 | C | G | 11 | a0001c0001t0001g0339 a0001c0001t0001g0340 a0002c0015t0003g0071 others(8): Show |
15 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+39C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767509 | |||||||
chr16:767510 | C | A | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+40C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767510 | |||||||
chr16:767515 | A | AGGAGCCC others(4): Show |
1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+49_1596+50ins others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767515 | ||||||
chr16:767525 | A | C | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+55A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767525 | |||||||
chr16:767525 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+55A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767525 | |||||||
chr16:767527 | T | C | 8 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(5): Show |
12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+57T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767527 | |||||||
chr16:767527 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+57T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767527 | |||||||
chr16:767528 | G | GGGGGGGT others(4): Show |
1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+60_1596+61ins others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767528 | ||||||
chr16:767534 | A | AGGGGCGT others(137): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+70_1596+71ins others(144): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767534 | ||||||
chr16:767540 | G | A | 3 | a0012c0017t0001g0082 a0012c0017t0001g0083 a0012c0017t0001g0184 |
3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1596+70G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767540 | |||||||
chr16:767540 | G | GCGTGGAG others(296): Show |
1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(303): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | ||||||
chr16:767540 | G | GCGTGGAG others(355): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | ||||||
chr16:767540 | G | GCGTGGAG others(242): Show |
1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(249): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | ||||||
chr16:767540 | G | GCGTGGAG others(302): Show |
1 | a0001c0001t0001g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(309): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767540 | ||||||
chr16:767541 | C | A | 8 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(5): Show |
12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+71C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767541 | |||||||
chr16:767541 | C | T | 20 | a0001c0021t0001g0175 a0001c0021t0001g0264 a0004c0006t0001g0179 others(17): Show |
20 | HG00558.hp1 HG00642.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1596+71C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767541 | |||||||
chr16:767542 | G | A | 1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1596+72G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767542 | |||||||
chr16:767542 | G | GC | 8 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(5): Show |
12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+72_1596+73ins others(1): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767542 | |||||||
chr16:767543 | T | G | 8 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(5): Show |
12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+73T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767543 | |||||||
chr16:767546 | A | AG | 48 | a0001c0001t0001g0061 a0001c0001t0001g0066 a0001c0001t0001g0076 others(45): Show |
57 | HG00642.hp1 HG00673.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.1596+83dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | ||||||
chr16:767546 | A | AGGAGGGG others(109): Show |
1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+78_1596+79ins others(116): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | ||||||
chr16:767546 | A | AGGGGGCC others(214): Show |
1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+81_1596+82ins others(221): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | ||||||
chr16:767546 | A | AGGGGGGA others(94): Show |
1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+82_1596+83ins others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | ||||||
chr16:767546 | A | AGGGGGGG others(590): Show |
1 | a0002c0002t0002g0296 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(597): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767546 | ||||||
chr16:767547 | G | GGGGGGGG others(392): Show |
1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767547 | ||||||
chr16:767547 | G | GGGGGGGG others(602): Show |
1 | a0002c0003t0004g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(609): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767547 | ||||||
chr16:767548 | G | GGGGGGGC others(208): Show |
1 | a0003c0004t0003g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(215): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767548 | ||||||
chr16:767549 | G | A | 10 | a0001c0001t0001g0084 a0002c0015t0003g0071 a0002c0015t0003g0172 others(7): Show |
14 | HG00423.hp2 HG00639.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+79G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767549 | |||||||
chr16:767549 | G | GGGGGGCG others(97): Show |
4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | HG02723.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(104): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767549 | ||||||
chr16:767549 | G | GGGGGGCG others(82): Show |
3 | a0011c0013t0006g0019 a0011c0013t0007g0205 a0011c0013t0007g0206 |
4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(89): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767549 | ||||||
chr16:767552 | G | GGCCAGTG others(125): Show |
1 | a0002c0002t0002g0294 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+84_1596+85ins others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGCCAGT others(127): Show |
1 | a0002c0002t0002g0297 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGCGAGT others(85): Show |
4 | a0004c0006t0001g0331 a0004c0006t0001g0335 a0004c0020t0001g0287 others(1): Show |
4 | HG00558.hp1 HG02602.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGCGAGT others(426): Show |
1 | a0001c0001t0001g0333 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(433): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGCGAGT others(112): Show |
1 | a0003c0004t0003g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(119): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGGCCAG others(128): Show |
1 | a0002c0002t0002g0316 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(135): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767552 | G | GGGGCGAG others(86): Show |
1 | a0004c0006t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767552 | ||||||
chr16:767553 | G | GGCCAGTG others(8): Show |
43 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0025 others(40): Show |
54 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | |||||||
chr16:767553 | G | GGCGAGTG others(8): Show |
37 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0001c0021t0001g0175 others(34): Show |
40 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | |||||||
chr16:767553 | G | GGGCCAGT others(9): Show |
7 | a0002c0002t0002g0195 a0002c0002t0002g0317 a0002c0002t0002g0318 others(4): Show |
7 | HG01109.hp1 HG01978.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | |||||||
chr16:767553 | G | GGGCGAGT others(9): Show |
2 | a0006c0008t0001g0035 a0008c0010t0002g0054 |
2 | HG02055.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1596+83_1596+84ins others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | |||||||
chr16:767553 | G | GGTGAGTG others(8): Show |
1 | a0002c0003t0004g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+83_1596+84ins others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767553 | |||||||
chr16:767554 | C | G | 5 | a0002c0003t0004g0216 a0003c0004t0003g0269 a0003c0004t0003g0337 others(2): Show |
5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+84C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767554 | |||||||
chr16:767555 | G | C | 105 | a0001c0001t0001g0164 a0001c0001t0001g0238 a0001c0001t0001g0246 others(102): Show |
119 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.1596+85G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767555 | |||||||
chr16:767556 | T | A | 42 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0084 others(39): Show |
53 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1596+86T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | |||||||
chr16:767556 | T | C | 23 | a0001c0001t0001g0086 a0001c0001t0001g0235 a0001c0001t0001g0236 others(20): Show |
28 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+86T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | |||||||
chr16:767556 | T | G | 95 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0001c0021t0001g0175 others(92): Show |
109 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1596+86T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767556 | |||||||
chr16:767557 | G | C | 1 | a0002c0003t0004g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1596+87G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767557 | |||||||
chr16:767558 | T | A | 12 | a0001c0001t0001g0333 a0002c0003t0004g0212 a0002c0003t0004g0216 others(9): Show |
12 | HG00558.hp1 HG01952.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+88T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | |||||||
chr16:767558 | T | C | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+88T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | |||||||
chr16:767558 | T | G | 7 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0085 others(4): Show |
7 | HG00280.hp1 HG02015.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+88T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767558 | |||||||
chr16:767558 | T | TG | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0088 others(8): Show |
11 | HG00642.hp2 HG01175.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+95dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767558 | ||||||
chr16:767559 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0085 |
3 | HG00280.hp1 HG02083.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1596+89G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767559 | |||||||
chr16:767559 | G | GGAGGGGG others(71): Show |
1 | a0001c0001t0001g0086 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+90_1596+91ins others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767559 | ||||||
chr16:767560 | G | GA | 14 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(11): Show |
19 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+90_1596+91ins others(1): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | |||||||
chr16:767560 | G | GAGGAGCC others(385): Show |
1 | a0002c0003t0004g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1596+90_1596+91ins others(392): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | |||||||
chr16:767560 | G | T | 5 | a0002c0003t0004g0216 a0003c0004t0003g0269 a0003c0004t0003g0337 others(2): Show |
5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+90G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767560 | |||||||
chr16:767561 | G | A | 135 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(132): Show |
160 | HG00099.hp2 HG00558.hp1 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.1596+91G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767561 | |||||||
chr16:767561 | G | GAGGAGGG others(147): Show |
1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1596+91_1596+92ins others(154): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767561 | |||||||
chr16:767561 | G | GGGGGCGC others(16): Show |
1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1596+95_1596+96ins others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767561 | ||||||
chr16:767563 | G | A | 5 | a0002c0003t0004g0216 a0003c0004t0003g0269 a0003c0004t0003g0337 others(2): Show |
5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+93G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767563 | |||||||
chr16:767564 | G | A | 39 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(36): Show |
50 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1596+94G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767564 | |||||||
chr16:767565 | GT | G | 40 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(37): Show |
51 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.1596+96delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767565 | |||||||
chr16:767566 | T | A | 5 | a0002c0003t0004g0216 a0003c0004t0003g0269 a0003c0004t0003g0337 others(2): Show |
5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+96T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | |||||||
chr16:767566 | T | C | 110 | a0001c0001t0001g0084 a0001c0001t0001g0157 a0001c0001t0001g0158 others(107): Show |
124 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.1596+96T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | |||||||
chr16:767566 | T | G | 2 | a0001c0001t0001g0277 a0002c0003t0004g0215 |
2 | HG01433.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+96T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767566 | |||||||
chr16:767566 | T | TGCGTGGA others(8): Show |
4 | a0001c0001t0001g0106 a0001c0001t0001g0120 a0001c0034t0001g0204 others(1): Show |
4 | HG00099.hp1 HG02015.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+121_1596+135d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | ||||||
chr16:767566 | T | TGCGTGGA others(405): Show |
1 | a0001c0001t0001g0005 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1596+135_1596+136i others(414): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | ||||||
chr16:767566 | T | TGCGTGGA others(390): Show |
1 | a0001c0001t0001g0005 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1596+163_1596+164i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | ||||||
chr16:767566 | T | TGCGTGGA others(954): Show |
1 | a0005c0005t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(963): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | ||||||
chr16:767566 | T | TGCGTGGA others(399): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+120_1596+121i others(408): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767566 | ||||||
chr16:767567 | G | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(36): Show |
50 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.1596+97G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767567 | |||||||
chr16:767567 | G | GC | 5 | a0002c0003t0004g0216 a0003c0004t0003g0269 a0003c0004t0003g0337 others(2): Show |
5 | HG02004.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+98dupC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767567 | ||||||
chr16:767568 | C | A | 2 | a0003c0004t0003g0263 a0004c0006t0001g0256 |
2 | HG00423.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1596+98C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767568 | |||||||
chr16:767569 | G | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(41): Show |
55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+99G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767569 | |||||||
chr16:767570 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(41): Show |
55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+100T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767570 | |||||||
chr16:767570 | T | G | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+100T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767570 | |||||||
chr16:767573 | A | AGGAGCCC others(4): Show |
1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+107_1596+108i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767573 | ||||||
chr16:767573 | A | T | 44 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(41): Show |
55 | HG00642.hp1 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.1596+103A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767573 | |||||||
chr16:767574 | G | GGGGGGAG others(54): Show |
1 | a0020c0038t0001g0276 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1596+105_1596+106i others(63): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767574 | ||||||
chr16:767575 | GA | G | 5 | a0002c0002t0002g0294 a0002c0002t0002g0297 a0002c0002t0002g0316 others(2): Show |
5 | HG02015.hp2 HG02132.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+106delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767575 | |||||||
chr16:767576 | A | AGGGGCGC others(445): Show |
1 | a0019c0044t0001g0043 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(454): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767576 | ||||||
chr16:767576 | A | AGGGGCGT others(7): Show |
1 | a0001c0001t0001g0138 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1596+112_1596+113i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767576 | ||||||
chr16:767576 | A | T | 3 | a0001c0037t0001g0087 a0012c0017t0001g0184 a0020c0038t0001g0276 |
3 | HG01099.hp2 HG01123.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1596+106A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767576 | |||||||
chr16:767580 | G | GCGCGTGG others(61): Show |
1 | a0002c0002t0002g0296 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767580 | ||||||
chr16:767581 | C | CGCGTGGA others(100): Show |
1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | ||||||
chr16:767581 | C | CGCGTGGA others(16): Show |
6 | a0001c0001t0001g0061 a0001c0001t0001g0159 a0001c0001t0001g0160 others(3): Show |
6 | HG01169.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+120_1596+121i others(25): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | ||||||
chr16:767581 | C | CGCGTGGA others(165): Show |
1 | a0001c0001t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(174): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | ||||||
chr16:767581 | C | CGCGTGGA others(164): Show |
1 | a0001c0001t0001g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(173): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | ||||||
chr16:767581 | C | CGCGTGGA others(163): Show |
1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767581 | ||||||
chr16:767581 | C | G | 3 | a0001c0037t0001g0087 a0012c0017t0001g0184 a0020c0038t0001g0276 |
3 | HG01099.hp2 HG01123.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.1596+111C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767581 | |||||||
chr16:767582 | G | A | 3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG02723.hp2 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+112G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767582 | |||||||
chr16:767582 | G | C | 4 | a0006c0011t0001g0022 a0006c0011t0001g0231 a0006c0011t0001g0232 others(1): Show |
5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+112G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767582 | |||||||
chr16:767583 | C | CGTGGAGG others(186): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(195): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767583 | ||||||
chr16:767583 | C | CGTGGAGG others(588): Show |
1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1596+120_1596+121i others(597): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767583 | ||||||
chr16:767585 | T | TGGAGGAG others(9): Show |
1 | a0001c0001t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1596+127_1596+128i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767585 | ||||||
chr16:767587 | GA | G | 14 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(11): Show |
19 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+118delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767587 | |||||||
chr16:767588 | A | G | 1 | a0002c0015t0003g0071 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1596+118A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767588 | |||||||
chr16:767590 | G | GGGGCCGT others(111): Show |
1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767590 | |||||||
chr16:767590 | G | GGGGCCGT others(1421): Show |
1 | a0002c0003t0001g0156 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1596+120_1596+121i others(1430): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767590 | |||||||
chr16:767591 | A | AGGAGGGG others(21): Show |
1 | a0001c0001t0001g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+123_1596+124i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | ||||||
chr16:767591 | A | AGGAGGGG others(121): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+123_1596+124i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | ||||||
chr16:767591 | A | AGGAGGGG others(162): Show |
1 | a0001c0001t0001g0086 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+123_1596+124i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767591 | ||||||
chr16:767591 | A | G | 23 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0235 others(20): Show |
28 | HG00639.hp1 HG00735.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+121A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767591 | |||||||
chr16:767596 | C | CGAGCGGG others(53): Show |
4 | a0006c0008t0001g0011 a0006c0008t0001g0032 a0006c0008t0001g0224 others(1): Show |
4 | HG02451.hp2 HG03139.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+127_1596+128i others(62): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767596 | ||||||
chr16:767596 | C | G | 3 | a0001c0001t0001g0177 a0002c0003t0001g0156 a0015c0022t0001g0029 |
3 | HG00735.hp2 HG01099.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1596+126C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767596 | |||||||
chr16:767596 | C | T | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+126C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767596 | |||||||
chr16:767596 | CGCGTGGA others(5): Show |
C | 1 | a0006c0011t0001g0230 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+128_1596+139d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767596 | ||||||
chr16:767597 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
5 | NA18953.hp1 NA19002.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+127G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767597 | |||||||
chr16:767597 | G | GAGCGGGA others(9): Show |
3 | a0006c0008t0001g0023 a0006c0008t0001g0035 a0006c0008t0001g0252 |
4 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+127_1596+128i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767597 | |||||||
chr16:767598 | C | A | 68 | a0001c0001t0001g0238 a0001c0021t0001g0175 a0002c0002t0002g0001 others(65): Show |
80 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.1596+128C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | |||||||
chr16:767598 | C | CATGGGGG others(3): Show |
1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+128_1596+129i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | |||||||
chr16:767598 | C | CGTGGAGG others(132): Show |
1 | a0002c0002t0002g0294 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+138_1596+139i others(141): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767598 | ||||||
chr16:767598 | C | CGTGGGGG others(3): Show |
1 | a0001c0001t0001g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1596+132_1596+133i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767598 | ||||||
chr16:767598 | C | G | 2 | a0002c0015t0003g0250 a0014c0045t0003g0039 |
2 | HG03579.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1596+128C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | |||||||
chr16:767598 | C | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG01099.hp1 HG02897.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+128C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767598 | |||||||
chr16:767599 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+129G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767599 | |||||||
chr16:767599 | G | GC | 63 | a0001c0001t0001g0238 a0001c0021t0001g0175 a0002c0002t0002g0001 others(60): Show |
74 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1596+129_1596+130i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767599 | |||||||
chr16:767600 | T | A | 2 | a0002c0015t0003g0250 a0014c0045t0003g0039 |
2 | HG03579.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1596+130T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767600 | |||||||
chr16:767600 | T | G | 63 | a0001c0001t0001g0238 a0001c0021t0001g0175 a0002c0002t0002g0001 others(60): Show |
74 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1596+130T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767600 | |||||||
chr16:767600 | T | TGGA | 29 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0219 others(26): Show |
36 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.1596+133_1596+135d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767600 | ||||||
chr16:767600 | TGGAGGG | T | 4 | a0006c0011t0001g0022 a0006c0011t0001g0231 a0006c0011t0001g0232 others(1): Show |
5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+133_1596+138d others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767600 | ||||||
chr16:767603 | A | AG | 8 | a0001c0001t0001g0065 a0001c0001t0001g0077 a0001c0001t0001g0154 others(5): Show |
8 | HG01952.hp2 HG02056.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+139dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767603 | ||||||
chr16:767604 | GGGGGGAG others(1): Show |
G | 5 | a0001c0001t0001g0164 a0007c0007t0001g0052 a0007c0007t0005g0020 others(2): Show |
6 | HG01070.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+136_1596+143d others(10): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767604 | ||||||
chr16:767605 | G | GA | 90 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0088 others(87): Show |
106 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | |||||||
chr16:767605 | G | GAGGA | 5 | a0004c0006t0001g0220 a0004c0006t0001g0331 a0004c0006t0001g0335 others(2): Show |
5 | HG00558.hp1 HG02602.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | |||||||
chr16:767605 | G | GAGGGGCG others(41): Show |
7 | a0002c0002t0002g0298 a0008c0010t0002g0013 a0008c0010t0002g0038 others(4): Show |
8 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+135_1596+136i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | |||||||
chr16:767605 | G | GAGGGGCG others(72): Show |
1 | a0014c0023t0002g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1596+135_1596+136i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767605 | |||||||
chr16:767606 | G | A | 9 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(6): Show |
9 | HG02055.hp2 HG02155.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+136G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767606 | |||||||
chr16:767608 | G | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0219 others(28): Show |
38 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596+138G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767608 | |||||||
chr16:767609 | G | C | 13 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0149 others(10): Show |
13 | HG01123.hp1 HG01169.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+139G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767609 | |||||||
chr16:767610 | A | C | 148 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0064 others(145): Show |
170 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.1596+140A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767610 | |||||||
chr16:767610 | A | G | 1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+140A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767610 | |||||||
chr16:767611 | G | A | 61 | a0001c0001t0001g0238 a0001c0021t0001g0175 a0002c0002t0002g0001 others(58): Show |
72 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1596+141G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767611 | |||||||
chr16:767611 | GC | G | 4 | a0006c0011t0001g0022 a0006c0011t0001g0231 a0006c0011t0001g0232 others(1): Show |
5 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+142delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767611 | |||||||
chr16:767612 | C | CGGGAG | 18 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0219 others(15): Show |
21 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+143_1596+144i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767612 | ||||||
chr16:767612 | C | T | 20 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0086 others(17): Show |
22 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+142C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767612 | |||||||
chr16:767613 | G | A | 6 | a0003c0004t0003g0223 a0004c0006t0001g0220 a0004c0006t0001g0331 others(3): Show |
6 | HG00558.hp1 HG02602.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+143G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | |||||||
chr16:767613 | G | GAGCGGGA others(46): Show |
1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+143_1596+144i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | |||||||
chr16:767613 | G | GGGA | 11 | a0002c0003t0002g0241 a0002c0003t0002g0242 a0002c0003t0002g0243 others(8): Show |
15 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+143_1596+144i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | |||||||
chr16:767613 | GTGGGGGG others(3): Show |
G | 1 | a0006c0011t0001g0230 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1596+144_1596+153d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767613 | |||||||
chr16:767614 | T | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(25): Show |
33 | HG00642.hp1 HG01069.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1596+144T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | |||||||
chr16:767614 | T | C | 1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+144T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | |||||||
chr16:767614 | T | G | 12 | a0002c0003t0002g0241 a0002c0003t0002g0242 a0002c0003t0002g0243 others(9): Show |
16 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+144T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767614 | |||||||
chr16:767614 | T | TG | 21 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0149 others(18): Show |
21 | HG00558.hp1 HG01123.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1596+150dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAC | 10 | a0002c0002t0002g0298 a0002c0003t0004g0210 a0002c0003t0004g0211 others(7): Show |
11 | HG01891.hp2 HG01978.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+146_1596+147i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGAG others(198): Show |
1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGAG others(40): Show |
2 | a0003c0004t0003g0266 a0003c0004t0003g0280 |
2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGAG others(106): Show |
1 | a0011c0013t0006g0019 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGAG others(108): Show |
2 | a0011c0013t0007g0205 a0011c0013t0007g0206 |
2 | HG02257.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(117): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(8): Show |
1 | a0001c0001t0001g0096 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1596+146_1596+147i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(351): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0097 |
3 | HG02257.hp1 HG03130.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1596+146_1596+147i others(360): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(352): Show |
1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(361): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(425): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(434): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(273): Show |
1 | a0002c0003t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(282): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(486): Show |
1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+146_1596+147i others(495): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGAGGGG others(384): Show |
1 | a0023c0040t0001g0168 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+146_1596+147i others(393): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGGGGGC others(521): Show |
1 | a0001c0001t0001g0116 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(530): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGGGGGC others(492): Show |
1 | a0005c0005t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(501): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767614 | T | TGGGGGGC others(557): Show |
1 | a0005c0005t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(566): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767614 | ||||||
chr16:767616 | G | A | 11 | a0002c0003t0002g0241 a0002c0003t0002g0242 a0002c0003t0002g0243 others(8): Show |
15 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+146G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767616 | |||||||
chr16:767616 | G | GAGGA | 71 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0001c0021t0001g0175 others(68): Show |
86 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1596+146_1596+147i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767616 | |||||||
chr16:767617 | G | A | 14 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0177 others(11): Show |
18 | HG00639.hp1 HG01891.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+147G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767617 | |||||||
chr16:767617 | G | C | 8 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(5): Show |
8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+147G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767617 | |||||||
chr16:767619 | G | A | 8 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(5): Show |
8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+149G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | C | 39 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0078 others(36): Show |
46 | HG00642.hp1 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.1596+149G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | GAGGAGGG others(148): Show |
2 | a0002c0002t0002g0297 a0002c0002t0002g0316 |
2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+149_1596+150i others(157): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | GAGGGGCG others(80): Show |
6 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(3): Show |
10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+149_1596+150i others(89): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | GCGTGGAG others(112): Show |
1 | a0001c0001t0001g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+149_1596+150i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | GGCGTGGA others(344): Show |
1 | a0001c0001t0001g0197 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1596+167_1596+168i others(353): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(217): Show |
2 | a0001c0001t0001g0149 a0001c0037t0001g0087 |
2 | HG02129.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1596+176_1596+177i others(226): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(314): Show |
1 | a0009c0012t0001g0201 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1596+191_1596+192i others(323): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(324): Show |
1 | a0001c0001t0001g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(333): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(290): Show |
1 | a0001c0001t0001g0336 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(299): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(1370): Show |
1 | a0001c0001t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1379): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(275): Show |
1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(284): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(382): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(391): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(149): Show |
1 | a0001c0001t0001g0277 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(158): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(1105): Show |
1 | a0001c0001t0001g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1114): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(1745): Show |
1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1754): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(321): Show |
1 | a0001c0001t0001g0115 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(330): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(335): Show |
1 | a0001c0009t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(344): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(782): Show |
1 | a0001c0001t0001g0075 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(791): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(338): Show |
1 | a0001c0001t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(294): Show |
1 | a0001c0001t0001g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(303): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(358): Show |
1 | a0005c0005t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(367): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(363): Show |
1 | a0005c0005t0009g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(372): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(518): Show |
1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(527): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(336): Show |
1 | a0001c0001t0001g0122 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(345): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(337): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0198 |
2 | HG02129.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(352): Show |
1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(361): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(604): Show |
1 | a0022c0036t0001g0126 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(613): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(337): Show |
1 | a0001c0001t0001g0016 | 2 | NA18940.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(338): Show |
1 | a0012c0017t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(1350): Show |
1 | a0001c0001t0001g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1359): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(493): Show |
2 | a0001c0001t0001g0128 a0001c0001t0005g0217 |
2 | HG01975.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(502): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(821): Show |
1 | a0024c0029t0001g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(830): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(919): Show |
1 | a0001c0001t0001g0332 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(928): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(620): Show |
1 | a0001c0001t0001g0094 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(629): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(2451): Show |
1 | a0001c0001t0001g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(2460): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(319): Show |
1 | a0009c0012t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(328): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(362): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(371): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(732): Show |
1 | a0001c0001t0001g0062 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(741): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(336): Show |
1 | a0001c0001t0001g0133 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(345): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(342): Show |
1 | a0009c0012t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(351): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(610): Show |
1 | a0001c0001t0001g0074 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(619): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(385): Show |
1 | a0001c0001t0001g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(394): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(505): Show |
1 | a0001c0001t0001g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(514): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(590): Show |
1 | a0001c0001t0001g0136 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(599): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(474): Show |
1 | a0001c0001t0001g0138 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(483): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(210): Show |
1 | a0004c0016t0001g0139 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(219): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(495): Show |
1 | a0001c0009t0001g0291 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(504): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(502): Show |
1 | a0001c0009t0001g0293 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(511): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(346): Show |
1 | a0001c0001t0001g0140 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(355): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(497): Show |
1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(506): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(389): Show |
1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(398): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(420): Show |
1 | a0001c0001t0001g0171 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(429): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(428): Show |
1 | a0018c0046t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(437): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(366): Show |
1 | a0021c0025t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(140): Show |
1 | a0005c0005t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(149): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(301): Show |
1 | a0001c0001t0008g0144 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(310): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(1390): Show |
1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+170_1596+171i others(1399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(270): Show |
1 | a0001c0001t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(279): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(364): Show |
1 | a0001c0001t0001g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(373): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(299): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+165_1596+166i others(308): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(371): Show |
1 | a0001c0001t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(380): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(340): Show |
1 | a0001c0001t0001g0145 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1596+163_1596+164i others(349): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(338): Show |
1 | a0001c0001t0001g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(347): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(353): Show |
1 | a0001c0001t0001g0326 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(147): Show |
1 | a0001c0001t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1596+158_1596+159i others(156): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGCGTGGA others(425): Show |
1 | a0005c0005t0001g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1596+158_1596+159i others(434): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGGCGTGG others(39): Show |
1 | a0001c0001t0001g0334 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(48): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGGGCGCA others(169): Show |
1 | a0002c0003t0004g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(178): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGGTGTGG others(59): Show |
1 | a0003c0004t0003g0222 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596+150_1596+151i others(68): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGGTGTGG others(72): Show |
1 | a0001c0001t0001g0163 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1596+150_1596+151i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GGGTGTGG others(58): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+150_1596+151i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | G | GTGTGTGG others(48): Show |
2 | a0001c0001t0001g0067 a0001c0001t0001g0155 |
2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1596+149_1596+150i others(57): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | G | T | 12 | a0002c0002t0002g0298 a0002c0003t0004g0210 a0002c0003t0004g0211 others(9): Show |
13 | HG01891.hp2 HG01978.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+149G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767619 | |||||||
chr16:767619 | GGCGTGGA others(8): Show |
G | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1596+174_1596+188d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | GGCGTGGA others(127): Show |
G | 2 | a0001c0001t0001g0340 a0010c0014t0001g0006 |
4 | HG00140.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+174_1596+307d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767619 | GGCGTGGA others(314): Show |
G | 1 | a0001c0009t0001g0290 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1596+174_1597-415d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767619 | ||||||
chr16:767620 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0021t0001g0264 others(4): Show |
8 | HG01109.hp2 HG01361.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+150G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | |||||||
chr16:767620 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1596+150G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | |||||||
chr16:767620 | G | GCGTGGAG others(475): Show |
1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(484): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767620 | ||||||
chr16:767620 | G | GGGCGCAT others(91): Show |
1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1596+150_1596+151i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767620 | |||||||
chr16:767621 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0002c0003t0004g0212 |
3 | HG01952.hp2 HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+151C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767621 | |||||||
chr16:767621 | C | T | 9 | a0001c0001t0001g0178 a0003c0004t0003g0223 a0003c0004t0003g0266 others(6): Show |
9 | HG00558.hp1 HG02486.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+151C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767621 | |||||||
chr16:767622 | G | GAGC | 83 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0001c0021t0001g0175 others(80): Show |
102 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.1596+152_1596+153i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767622 | |||||||
chr16:767622 | G | GTGGAGGA others(337): Show |
1 | a0001c0001t0001g0084 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(346): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767622 | ||||||
chr16:767622 | GT | G | 8 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(5): Show |
8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+153delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767622 | |||||||
chr16:767623 | T | A | 1 | a0004c0016t0001g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+153T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | |||||||
chr16:767623 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0002c0003t0004g0212 |
3 | HG01952.hp2 HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+153T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | |||||||
chr16:767623 | T | G | 85 | a0001c0001t0001g0072 a0001c0001t0001g0238 a0001c0001t0001g0246 others(82): Show |
104 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.1596+153T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767623 | |||||||
chr16:767624 | G | C | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+154G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767624 | |||||||
chr16:767625 | G | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0153 |
2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+155G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767625 | |||||||
chr16:767626 | A | C | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+156A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767626 | |||||||
chr16:767626 | AGG | A | 4 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0227 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+157_1596+158d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767626 | |||||||
chr16:767627 | G | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0153 |
2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+157G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767627 | |||||||
chr16:767627 | GGA | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0177 others(6): Show |
10 | HG01069.hp2 HG01071.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+159_1596+160d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767627 | ||||||
chr16:767627 | GGAGGGGC others(71): Show |
G | 1 | a0012c0017t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1596+159_1596+236d others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767627 | ||||||
chr16:767628 | G | T | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+158G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767628 | |||||||
chr16:767628 | GA | G | 13 | a0002c0002t0002g0296 a0003c0004t0003g0223 a0003c0004t0003g0263 others(10): Show |
13 | HG00423.hp2 HG00558.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+159delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767628 | |||||||
chr16:767629 | A | AGGGGCGC others(374): Show |
1 | a0001c0001t0001g0105 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(383): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(604): Show |
1 | a0001c0001t0001g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(613): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(83): Show |
1 | a0001c0001t0001g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(481): Show |
1 | a0001c0034t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(490): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(420): Show |
1 | a0005c0005t0001g0036 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(429): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(548): Show |
1 | a0005c0005t0001g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(557): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(349): Show |
1 | a0005c0005t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(358): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(496): Show |
1 | a0001c0001t0001g0004 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(505): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(470): Show |
1 | a0012c0017t0001g0082 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(479): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(626): Show |
1 | a0001c0001t0001g0005 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(635): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGC others(551): Show |
1 | a0010c0014t0001g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(560): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGCGT others(681): Show |
1 | a0005c0005t0001g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(690): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | AGGGGTGC others(17): Show |
1 | a0001c0001t0001g0146 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767629 | ||||||
chr16:767629 | A | C | 4 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0227 others(1): Show |
5 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+159A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | |||||||
chr16:767629 | A | G | 10 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0001c0001t0001g0219 others(7): Show |
11 | HG01099.hp1 HG01952.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+159A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | |||||||
chr16:767629 | A | T | 1 | a0001c0001t0001g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1596+159A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767629 | |||||||
chr16:767632 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+162G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767632 | |||||||
chr16:767633 | G | GCGCGTGG others(166): Show |
3 | a0001c0001t0001g0093 a0001c0001t0001g0199 a0009c0012t0001g0325 |
3 | NA19002.hp1 NA19083.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | ||||||
chr16:767633 | G | GCGCGTGG others(732): Show |
1 | a0001c0001t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(741): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | ||||||
chr16:767633 | G | GCGCGTGG others(166): Show |
1 | a0001c0001t0001g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | ||||||
chr16:767633 | G | GCGCGTGG others(138): Show |
1 | a0001c0009t0001g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | ||||||
chr16:767633 | G | GCGCGTGG others(168): Show |
1 | a0001c0001t0001g0324 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(177): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767633 | ||||||
chr16:767633 | G | GTGCGTGG others(166): Show |
1 | a0001c0039t0001g0147 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+163_1596+164i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767633 | |||||||
chr16:767633 | G | T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0152 a0001c0001t0001g0177 others(1): Show |
4 | HG02083.hp2 HG02602.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+163G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767633 | |||||||
chr16:767634 | C | CGAGCGGG others(38): Show |
1 | a0001c0001t0001g0246 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(47): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGAGCGGG others(22): Show |
3 | a0002c0003t0002g0241 a0002c0003t0002g0242 a0002c0003t0004g0207 |
3 | HG02647.hp1 HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1596+165_1596+166i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(6): Show |
6 | a0002c0002t0002g0010 a0002c0002t0002g0059 a0002c0002t0002g0301 others(3): Show |
8 | HG00733.hp2 HG01109.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+171_1596+172i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(138): Show |
2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+176_1596+177i others(147): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(269): Show |
1 | a0001c0001t0001g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596+176_1596+177i others(278): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(17): Show |
5 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(2): Show |
5 | HG03492.hp1 HG03710.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+173_1596+174i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(591): Show |
1 | a0005c0005t0001g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(600): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(363): Show |
1 | a0001c0001t0001g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(372): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(286): Show |
1 | a0001c0001t0001g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(295): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(518): Show |
1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(527): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(492): Show |
1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(501): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(307): Show |
1 | a0001c0001t0001g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(316): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(444): Show |
1 | a0001c0001t0001g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(453): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(1853): Show |
1 | a0001c0001t0001g0130 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(1862): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(513): Show |
1 | a0002c0003t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(522): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(537): Show |
1 | a0001c0001t0001g0081 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(546): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(353): Show |
1 | a0001c0001t0001g0077 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(362): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(16): Show |
1 | a0001c0009t0001g0024 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(25): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGCGTGGA others(111): Show |
1 | a0001c0001t0001g0165 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | CGTGTGGA others(253): Show |
1 | a0001c0001t0001g0162 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1596+165_1596+166i others(262): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767634 | ||||||
chr16:767634 | C | G | 5 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0146 others(2): Show |
5 | HG00558.hp2 HG01952.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+164C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767634 | |||||||
chr16:767634 | C | T | 9 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0227 others(6): Show |
11 | HG01069.hp2 HG01071.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+164C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767634 | |||||||
chr16:767635 | G | A | 13 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(10): Show |
17 | HG01099.hp1 HG02055.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+165G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767635 | |||||||
chr16:767636 | C | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0164 others(14): Show |
20 | HG01070.hp1 HG01109.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1596+166C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | |||||||
chr16:767636 | C | CATGGGGG others(3): Show |
1 | a0004c0016t0001g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+166_1596+167i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | |||||||
chr16:767636 | C | CGTGGAGG others(163): Show |
1 | a0001c0001t0010g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767636 | ||||||
chr16:767636 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+166C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | |||||||
chr16:767636 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0001g0159 others(3): Show |
6 | HG00609.hp1 HG02145.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+166C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767636 | |||||||
chr16:767637 | G | GC | 16 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0021t0001g0264 others(13): Show |
19 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+167_1596+168i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767637 | |||||||
chr16:767638 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+168T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767638 | |||||||
chr16:767638 | T | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0021t0001g0264 others(13): Show |
19 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+168T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767638 | |||||||
chr16:767639 | GGA | G | 6 | a0008c0010t0002g0013 a0008c0010t0002g0038 a0008c0010t0002g0053 others(3): Show |
7 | HG01891.hp2 HG02559.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+171_1596+172d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767639 | ||||||
chr16:767640 | GA | G | 5 | a0002c0003t0004g0208 a0002c0003t0004g0210 a0006c0011t0001g0230 others(2): Show |
5 | HG01978.hp1 HG02055.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+171delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767640 | |||||||
chr16:767641 | A | AGGGGGCC others(225): Show |
1 | a0001c0001t0001g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(234): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767641 | ||||||
chr16:767641 | A | AGGGGGCC others(242): Show |
1 | a0001c0001t0001g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(251): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767641 | ||||||
chr16:767641 | A | G | 1 | a0002c0003t0004g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+171A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767641 | |||||||
chr16:767641 | AGG | A | 45 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0026 others(42): Show |
54 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+172_1596+173d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767641 | |||||||
chr16:767642 | G | GGGGGCCG others(3): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(125): Show |
1 | a0001c0001t0001g0118 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(360): Show |
1 | a0001c0001t0001g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(369): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(1467): Show |
1 | a0001c0001t0001g0017 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1596+173_1596+174i others(1476): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(111): Show |
1 | a0001c0001t0001g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(286): Show |
1 | a0001c0001t0001g0170 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(295): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGCCG others(383): Show |
1 | a0001c0001t0001g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(392): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | G | GGGGGGCC others(47): Show |
1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1596+173_1596+174i others(56): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767642 | GGA | G | 14 | a0001c0001t0001g0238 a0002c0002t0002g0298 a0002c0015t0003g0249 others(11): Show |
18 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+174_1596+175d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767642 | ||||||
chr16:767643 | G | GGGGCCGT others(45): Show |
1 | a0005c0005t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+173_1596+174i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767643 | |||||||
chr16:767643 | GA | G | 16 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0096 others(13): Show |
16 | HG00544.hp2 HG00609.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+174delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767643 | |||||||
chr16:767644 | A | AGGAGGGG others(20): Show |
1 | a0002c0002t0002g0296 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+176_1596+177i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767644 | ||||||
chr16:767644 | A | AGGAGGGG others(224): Show |
1 | a0002c0003t0004g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1596+176_1596+177i others(233): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767644 | ||||||
chr16:767644 | A | C | 45 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0026 others(42): Show |
54 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1596+174A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767644 | |||||||
chr16:767644 | A | G | 30 | a0001c0001t0001g0017 a0001c0001t0001g0065 a0001c0001t0001g0090 others(27): Show |
32 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.1596+174A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767644 | |||||||
chr16:767648 | G | C | 5 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0193 others(2): Show |
5 | HG00544.hp2 HG01081.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+178G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767648 | |||||||
chr16:767649 | C | CGTGTGGG others(5): Show |
1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+180_1596+181i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767649 | ||||||
chr16:767649 | C | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0005c0005t0001g0034 others(1): Show |
4 | NA18966.hp1 NA18995.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+179C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767649 | |||||||
chr16:767649 | C | T | 57 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0001c0001t0001g0238 others(54): Show |
70 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1596+179C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767649 | |||||||
chr16:767649 | CGCGTGGA others(5): Show |
C | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+181_1596+192d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767649 | ||||||
chr16:767650 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0007c0007t0001g0052 others(3): Show |
7 | HG02280.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+180G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767650 | |||||||
chr16:767651 | C | A | 10 | a0001c0001t0001g0218 a0002c0002t0002g0284 a0002c0003t0002g0247 others(7): Show |
14 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+181C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767651 | |||||||
chr16:767651 | C | CGTGGGGG others(3): Show |
2 | a0002c0002t0002g0297 a0002c0002t0002g0316 |
2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+185_1596+186i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767651 | ||||||
chr16:767651 | C | T | 13 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0001g0100 others(10): Show |
13 | HG00544.hp2 HG00558.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+181C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767651 | |||||||
chr16:767652 | G | A | 2 | a0001c0001t0001g0237 a0004c0016t0001g0258 |
2 | HG03195.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1596+182G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767652 | |||||||
chr16:767652 | G | GC | 7 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0007c0007t0001g0007 others(4): Show |
11 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+182_1596+183i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767652 | |||||||
chr16:767653 | T | G | 7 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0007c0007t0001g0007 others(4): Show |
11 | HG02055.hp1 HG02155.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+183T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767653 | |||||||
chr16:767654 | GGAGGGGG others(6): Show |
G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0193 |
3 | HG00544.hp2 HG01081.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1596+186_1596+198d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767654 | ||||||
chr16:767654 | GGAGGGGG others(125): Show |
G | 1 | a0001c0001t0001g0272 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1596+186_1596+317d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767654 | ||||||
chr16:767655 | GA | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
8 | HG01981.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+186delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767655 | |||||||
chr16:767655 | GAGGGGGG others(124): Show |
G | 1 | a0002c0003t0001g0089 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1596+186_1596+316d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767655 | |||||||
chr16:767656 | A | ACGGGGTG others(7): Show |
1 | a0002c0003t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1596+186_1596+187i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767656 | |||||||
chr16:767656 | A | AG | 9 | a0001c0001t0001g0075 a0001c0001t0001g0095 a0001c0001t0001g0104 others(6): Show |
9 | HG00408.hp1 HG01175.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+192dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767656 | ||||||
chr16:767656 | A | G | 22 | a0001c0001t0001g0106 a0001c0001t0001g0219 a0001c0001t0001g0237 others(19): Show |
26 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+186A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767656 | |||||||
chr16:767657 | G | A | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+187G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | |||||||
chr16:767657 | G | C | 1 | a0002c0002t0002g0060 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1596+187G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | |||||||
chr16:767657 | G | T | 1 | a0005c0005t0001g0050 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1596+187G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767657 | |||||||
chr16:767657 | GGGGGGAG others(3): Show |
G | 3 | a0006c0011t0001g0230 a0007c0007t0001g0052 a0015c0022t0001g0030 |
3 | HG02280.hp2 HG02615.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+202d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767657 | ||||||
chr16:767657 | GGGGGGAG others(122): Show |
G | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+321d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767657 | ||||||
chr16:767658 | G | A | 1 | a0002c0003t0002g0243 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1596+188G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | |||||||
chr16:767658 | G | C | 1 | a0008c0010t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1596+188G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | |||||||
chr16:767658 | G | GA | 80 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0108 others(77): Show |
98 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596+188_1596+189i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | |||||||
chr16:767658 | G | GAGGA | 9 | a0001c0001t0001g0339 a0002c0002t0002g0298 a0004c0006t0001g0220 others(6): Show |
9 | HG00558.hp1 HG00642.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+188_1596+189i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767658 | |||||||
chr16:767658 | GGGGGAGC others(40): Show |
G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0153 |
2 | HG03927.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1596+193_1596+239d others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767658 | ||||||
chr16:767659 | G | A | 1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+189G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767659 | |||||||
chr16:767660 | G | GTCGCGT | 3 | a0003c0004t0003g0223 a0003c0004t0003g0266 a0003c0004t0003g0280 |
3 | HG02486.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1596+190_1596+191i others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767660 | |||||||
chr16:767662 | G | C | 18 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0093 others(15): Show |
19 | HG00099.hp1 HG01952.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+192G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767662 | |||||||
chr16:767662 | G | T | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+192G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767662 | |||||||
chr16:767663 | A | C | 183 | a0001c0001t0001g0008 a0001c0001t0001g0051 a0001c0001t0001g0078 others(180): Show |
213 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(210): Show |
intron_variant | MODIFIER | c.1596+193A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | |||||||
chr16:767663 | A | G | 2 | a0001c0001t0001g0237 a0005c0005t0001g0050 |
2 | HG03195.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1596+193A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | |||||||
chr16:767663 | A | T | 2 | a0001c0001t0001g0109 a0008c0010t0002g0251 |
2 | HG03209.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1596+193A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767663 | |||||||
chr16:767664 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1596+194G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767664 | |||||||
chr16:767664 | GC | G | 4 | a0002c0002t0002g0060 a0003c0004t0003g0223 a0003c0004t0003g0266 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+195delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767664 | |||||||
chr16:767665 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+195C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767665 | |||||||
chr16:767665 | C | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0090 others(16): Show |
20 | HG00099.hp1 HG02040.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596+195C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767665 | |||||||
chr16:767666 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0001g0159 others(11): Show |
14 | HG00558.hp1 HG00609.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+196G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767666 | |||||||
chr16:767666 | GTGGGGGG others(3): Show |
G | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+197_1596+206d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767666 | |||||||
chr16:767667 | T | A | 5 | a0001c0001t0001g0072 a0002c0002t0002g0060 a0003c0004t0003g0223 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+197T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767667 | |||||||
chr16:767667 | T | G | 2 | a0001c0001t0001g0237 a0004c0006t0001g0335 |
2 | HG03195.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1596+197T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767667 | |||||||
chr16:767667 | T | TG | 30 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0093 others(27): Show |
34 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596+203dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | ||||||
chr16:767667 | T | TGGAG | 9 | a0001c0021t0001g0264 a0006c0011t0001g0022 a0006c0011t0001g0231 others(6): Show |
14 | HG01361.hp1 HG01981.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | ||||||
chr16:767667 | T | TGGAGG | 27 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0219 others(24): Show |
32 | HG00733.hp2 HG00738.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | ||||||
chr16:767667 | T | TGGAGGAG others(40): Show |
1 | a0001c0001t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+199_1596+200i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767667 | ||||||
chr16:767668 | G | GGA | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767668 | ||||||
chr16:767668 | GGGGGGCG others(57): Show |
G | 1 | a0001c0001t0001g0164 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1596+199_1596+262d others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767668 | |||||||
chr16:767668 | GGGGGGCG others(111): Show |
G | 1 | a0001c0001t0001g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1596+204_1596+321d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767668 | ||||||
chr16:767669 | G | GAGGA | 12 | a0004c0006t0001g0234 a0004c0006t0001g0256 a0008c0010t0002g0013 others(9): Show |
13 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+199_1596+200i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767669 | |||||||
chr16:767670 | G | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0203 a0002c0002t0002g0296 others(2): Show |
5 | HG01346.hp2 HG02056.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+200G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767670 | |||||||
chr16:767671 | G | A | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+201G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767671 | |||||||
chr16:767672 | G | C | 40 | a0001c0001t0001g0008 a0001c0001t0001g0072 a0001c0001t0001g0078 others(37): Show |
45 | HG00733.hp2 HG00738.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1596+202G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | |||||||
chr16:767672 | G | GCGCGTGG others(75): Show |
1 | a0001c0001t0001g0150 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1596+202_1596+203i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | |||||||
chr16:767672 | G | GGCGGCGT others(50): Show |
1 | a0001c0001t0001g0197 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1596+205_1596+206i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGCGTGGA others(8): Show |
3 | a0005c0005t0001g0036 a0005c0005t0001g0040 a0019c0044t0001g0043 |
3 | HG00609.hp2 HG00738.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1596+212_1596+226d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGCGTGGA others(64): Show |
1 | a0001c0001t0001g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1596+230_1596+231i others(73): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGCGTGA others(57): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGCGTGG others(248): Show |
1 | a0001c0001t0001g0281 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(257): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGCGTGG others(8): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGCGTGG others(91): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0159 a0001c0001t0001g0160 |
3 | HG00609.hp1 HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGGCGCA others(21): Show |
1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGGGC | 44 | a0001c0001t0001g0238 a0002c0002t0002g0001 a0002c0002t0002g0025 others(41): Show |
57 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.1596+203_1596+204i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(34): Show |
3 | a0004c0006t0001g0220 a0004c0006t0001g0331 a0004c0020t0001g0287 |
3 | HG00558.hp1 HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(314): Show |
1 | a0016c0027t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1596+203_1596+204i others(323): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(58): Show |
1 | a0001c0001t0001g0162 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(87): Show |
2 | a0001c0001t0001g0123 a0001c0001t0010g0137 |
2 | HG02027.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1596+203_1596+204i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(63): Show |
1 | a0001c0001t0001g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(72): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | GGGTGTGG others(219): Show |
1 | a0001c0001t0001g0086 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1596+203_1596+204i others(228): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767672 | ||||||
chr16:767672 | G | T | 15 | a0001c0001t0001g0109 a0002c0002t0002g0284 a0002c0003t0002g0247 others(12): Show |
20 | HG01981.hp1 HG02055.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596+202G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767672 | |||||||
chr16:767674 | C | A | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+204C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | |||||||
chr16:767674 | C | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+204C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | |||||||
chr16:767674 | C | T | 19 | a0001c0001t0001g0107 a0001c0001t0001g0154 a0001c0001t0001g0178 others(16): Show |
24 | HG00639.hp1 HG00642.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.1596+204C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767674 | |||||||
chr16:767676 | T | A | 3 | a0003c0004t0003g0263 a0004c0006t0001g0234 a0004c0006t0001g0256 |
3 | HG00423.hp2 HG04204.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1596+206T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | |||||||
chr16:767676 | T | C | 17 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0112 others(14): Show |
18 | HG00558.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+206T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | |||||||
chr16:767676 | T | G | 12 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(9): Show |
12 | HG01884.hp1 HG02071.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+206T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767676 | |||||||
chr16:767678 | G | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+208G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767678 | |||||||
chr16:767678 | G | T | 9 | a0001c0001t0001g0108 a0008c0010t0002g0013 a0008c0010t0002g0038 others(6): Show |
10 | HG01891.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+208G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767678 | |||||||
chr16:767679 | A | AGGGGGGC others(14): Show |
1 | a0002c0002t0002g0294 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1596+211_1596+212i others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767679 | ||||||
chr16:767679 | A | C | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+209A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767679 | |||||||
chr16:767679 | A | G | 10 | a0001c0001t0001g0108 a0008c0010t0002g0013 a0008c0010t0002g0038 others(7): Show |
11 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+209A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767679 | |||||||
chr16:767680 | G | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG00558.hp2 HG03492.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+210G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767680 | |||||||
chr16:767680 | GGAGGGGC others(18): Show |
G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0193 |
2 | HG00544.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1596+212_1596+236d others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767680 | ||||||
chr16:767681 | G | C | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+211G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767681 | |||||||
chr16:767681 | GA | G | 75 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(72): Show |
93 | HG00099.hp2 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1596+212delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767681 | |||||||
chr16:767682 | A | AGGGGCGC others(6): Show |
2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+223_1596+224i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767682 | ||||||
chr16:767682 | A | ATG | 11 | a0001c0021t0001g0175 a0004c0006t0001g0179 a0004c0006t0001g0183 others(8): Show |
11 | HG02071.hp2 HG02080.hp2 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+212_1596+213i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767682 | |||||||
chr16:767682 | A | G | 16 | a0001c0001t0001g0108 a0002c0002t0002g0187 a0002c0002t0002g0283 others(13): Show |
17 | HG01891.hp2 HG02015.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+212A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767682 | |||||||
chr16:767687 | C | G | 18 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0113 others(15): Show |
18 | HG00558.hp2 HG02071.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+217C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767687 | |||||||
chr16:767687 | C | T | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+217C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767687 | |||||||
chr16:767688 | G | A | 1 | a0015c0022t0001g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1596+218G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767688 | |||||||
chr16:767689 | C | CATGGGGG others(4): Show |
1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+219_1596+220i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | |||||||
chr16:767689 | C | CATGGGGG others(3): Show |
1 | a0004c0006t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1596+219_1596+220i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | |||||||
chr16:767689 | C | CGTGGGGG others(3): Show |
1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+223_1596+224i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767689 | ||||||
chr16:767689 | C | T | 13 | a0001c0001t0001g0051 a0001c0001t0001g0106 a0001c0021t0001g0175 others(10): Show |
13 | HG00099.hp1 HG02071.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+219C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767689 | |||||||
chr16:767690 | G | A | 2 | a0001c0001t0001g0108 a0003c0004t0003g0263 |
2 | HG00423.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+220G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767690 | |||||||
chr16:767691 | TGGAGGGG others(20): Show |
T | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+227_1596+253d others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767691 | ||||||
chr16:767692 | G | GGGAGGAG others(8): Show |
1 | a0001c0001t0001g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1596+223_1596+224i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767692 | ||||||
chr16:767692 | GGA | G | 8 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(5): Show |
13 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+224_1596+225d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767692 | ||||||
chr16:767694 | A | G | 7 | a0001c0001t0001g0108 a0002c0002t0002g0284 a0002c0003t0002g0247 others(4): Show |
7 | HG00423.hp2 HG02155.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+224A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767694 | |||||||
chr16:767694 | AGGGGGGA others(4): Show |
A | 6 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(3): Show |
6 | HG02523.hp2 HG03579.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+231_1596+241d others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767694 | ||||||
chr16:767694 | AGGGGGGA others(42): Show |
A | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+227_1596+275d others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767694 | ||||||
chr16:767695 | G | GGAGGAGG others(7): Show |
1 | a0002c0003t0004g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+226_1596+227i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | ||||||
chr16:767695 | G | GGAGGAGG others(112): Show |
1 | a0002c0003t0004g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+226_1596+227i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | ||||||
chr16:767695 | GGGGGGAG others(3): Show |
G | 1 | a0001c0001t0001g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+231_1596+240d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767695 | ||||||
chr16:767696 | G | GA | 64 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0078 others(61): Show |
78 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1596+226_1596+227i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767696 | |||||||
chr16:767696 | G | T | 7 | a0001c0001t0001g0219 a0006c0008t0001g0011 a0006c0008t0001g0023 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+226G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767696 | |||||||
chr16:767696 | GGGGGAGT others(30): Show |
G | 1 | a0017c0019t0002g0286 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1596+231_1596+267d others(39): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767696 | ||||||
chr16:767697 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+227G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767697 | |||||||
chr16:767697 | G | T | 1 | a0003c0004t0003g0270 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1596+227G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767697 | |||||||
chr16:767699 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0238 a0003c0004t0003g0270 |
3 | HG02717.hp1 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+229G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | |||||||
chr16:767699 | G | GC | 20 | a0001c0001t0001g0170 a0001c0001t0001g0246 a0002c0002t0002g0010 others(17): Show |
23 | HG00738.hp1 HG01109.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+229_1596+230i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | |||||||
chr16:767699 | G | GCACGTGG others(22): Show |
1 | a0002c0002t0002g0298 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1596+229_1596+230i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | |||||||
chr16:767699 | G | GT | 5 | a0002c0003t0004g0021 a0002c0003t0004g0207 a0002c0003t0004g0226 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+229_1596+230i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | |||||||
chr16:767699 | G | T | 9 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(6): Show |
14 | HG00423.hp2 HG00639.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+229G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767699 | |||||||
chr16:767700 | G | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0015 others(107): Show |
116 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1596+230G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767700 | |||||||
chr16:767700 | G | GCGCGTGG others(928): Show |
1 | a0001c0001t0001g0103 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1596+230_1596+231i others(937): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767700 | |||||||
chr16:767701 | A | ACGTG | 7 | a0001c0001t0001g0219 a0006c0008t0001g0011 a0006c0008t0001g0023 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+231_1596+232i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | |||||||
chr16:767701 | A | C | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(263): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.1596+231A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | |||||||
chr16:767701 | A | G | 3 | a0001c0001t0001g0170 a0002c0003t0004g0210 a0002c0003t0004g0212 |
3 | HG01952.hp2 HG01978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1596+231A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | |||||||
chr16:767701 | A | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0112 others(8): Show |
11 | HG00423.hp2 HG00558.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+231A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767701 | |||||||
chr16:767703 | T | A | 7 | a0001c0001t0001g0219 a0006c0008t0001g0011 a0006c0008t0001g0023 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+233T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | |||||||
chr16:767703 | T | C | 151 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(148): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1596+233T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | |||||||
chr16:767703 | T | G | 3 | a0001c0001t0001g0108 a0003c0004t0003g0263 a0003c0004t0003g0270 |
3 | HG00423.hp2 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1596+233T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767703 | |||||||
chr16:767703 | T | TG | 5 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0002t0002g0298 others(2): Show |
5 | HG02630.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+234dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767703 | ||||||
chr16:767703 | T | TGGA | 25 | a0001c0001t0001g0238 a0001c0001t0001g0246 a0002c0002t0002g0010 others(22): Show |
28 | HG00738.hp1 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1596+234_1596+235i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767703 | ||||||
chr16:767704 | G | A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0155 a0001c0021t0001g0264 others(3): Show |
6 | HG00423.hp2 HG01361.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+234G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767704 | |||||||
chr16:767704 | G | GGAGGAGC others(111): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+234_1596+235i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767704 | |||||||
chr16:767705 | T | A | 5 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0002t0002g0298 others(2): Show |
5 | HG02630.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+235T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767705 | |||||||
chr16:767705 | T | G | 47 | a0001c0001t0001g0108 a0001c0001t0001g0219 a0001c0001t0001g0238 others(44): Show |
56 | HG00423.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1596+235T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767705 | |||||||
chr16:767705 | T | TGGA | 59 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0112 others(56): Show |
77 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | ||||||
chr16:767705 | T | TGGAGGGG others(21): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0115 a0001c0001t0001g0125 others(4): Show |
7 | HG00639.hp2 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | ||||||
chr16:767705 | T | TGGAGGGG others(317): Show |
1 | a0005c0005t0001g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(326): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | ||||||
chr16:767705 | T | TGGAGGGG others(127): Show |
1 | a0005c0005t0001g0196 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | ||||||
chr16:767705 | TG | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0092 others(10): Show |
13 | HG00280.hp2 HG00642.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+242delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767705 | ||||||
chr16:767706 | G | A | 46 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0001c0001t0001g0219 others(43): Show |
55 | HG00639.hp1 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1596+236G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767706 | |||||||
chr16:767706 | G | C | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+236G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767706 | |||||||
chr16:767706 | G | GGAGGA | 23 | a0001c0001t0001g0080 a0001c0001t0001g0113 a0001c0001t0001g0114 others(20): Show |
23 | HG00558.hp2 HG01934.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+237_1596+238i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | ||||||
chr16:767706 | G | GGAGGAGG others(26): Show |
1 | a0006c0008t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(35): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | ||||||
chr16:767706 | G | GGAGGGGG others(75): Show |
1 | a0005c0005t0001g0046 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1596+237_1596+238i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | ||||||
chr16:767706 | G | GGGGGGGC others(162): Show |
1 | a0001c0001t0001g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | ||||||
chr16:767706 | G | GGGGGGGC others(45): Show |
1 | a0001c0001t0001g0198 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767706 | ||||||
chr16:767708 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0112 others(9): Show |
17 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596+238G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767708 | |||||||
chr16:767710 | G | T | 1 | a0004c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596+240G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767710 | |||||||
chr16:767711 | G | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0080 others(131): Show |
151 | HG00099.hp2 HG00423.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1596+241G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | |||||||
chr16:767711 | G | GCGTGGAG others(167): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+241_1596+242i others(176): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | |||||||
chr16:767711 | G | GCGTGGAG others(456): Show |
1 | a0020c0038t0001g0276 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1596+241_1596+242i others(465): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | |||||||
chr16:767711 | G | GCGTGGAG others(6): Show |
1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+241_1596+242i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | |||||||
chr16:767711 | G | GGAGTGTG others(515): Show |
1 | a0001c0001t0001g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(524): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGCGTG others(33): Show |
2 | a0002c0003t0004g0214 a0002c0003t0004g0215 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+244_1596+245i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGGTGG others(8): Show |
1 | a0001c0001t0001g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+244_1596+245i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(8): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0104 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(46): Show |
1 | a0001c0001t0001g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(99): Show |
1 | a0009c0012t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(553): Show |
1 | a0001c0009t0001g0024 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(562): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(552): Show |
1 | a0001c0009t0001g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(561): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(366): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(74): Show |
2 | a0004c0016t0001g0139 a0004c0016t0001g0257 |
2 | HG03834.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(784): Show |
1 | a0001c0001t0001g0014 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(793): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(688): Show |
1 | a0001c0001t0001g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(697): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(405): Show |
1 | a0001c0001t0001g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(414): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(351): Show |
1 | a0001c0001t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(360): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(432): Show |
1 | a0001c0001t0001g0004 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(441): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(373): Show |
1 | a0001c0001t0001g0004 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(382): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(7): Show |
61 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
63 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+250_1596+251i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(498): Show |
1 | a0001c0001t0001g0336 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(507): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(155): Show |
1 | a0001c0001t0008g0144 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(164): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(49): Show |
1 | a0001c0001t0001g0134 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(102): Show |
1 | a0001c0037t0001g0087 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(111): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(179): Show |
1 | a0001c0001t0001g0149 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(188): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGCGTGGA others(8): Show |
1 | a0010c0014t0001g0102 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(33): Show |
1 | a0001c0009t0001g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(20): Show |
1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(156): Show |
1 | a0001c0001t0001g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(20): Show |
1 | a0001c0001t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(35): Show |
1 | a0001c0001t0001g0118 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(44): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(156): Show |
1 | a0001c0001t0001g0004 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(238): Show |
1 | a0001c0001t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(247): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(156): Show |
1 | a0024c0029t0001g0129 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(165): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(34): Show |
1 | a0001c0034t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(36): Show |
2 | a0001c0001t0001g0105 a0012c0017t0001g0082 |
2 | HG01256.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1596+242_1596+243i others(45): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGCAT others(73): Show |
1 | a0001c0001t0001g0081 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(82): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGTGG others(8): Show |
2 | a0001c0001t0001g0095 a0021c0025t0001g0167 |
2 | HG01175.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1596+242_1596+243i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGGCGTGG others(11): Show |
1 | a0023c0040t0001g0168 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(20): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGCGTG others(498): Show |
1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(507): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(21): Show |
1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(125): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(245): Show |
1 | a0001c0001t0001g0130 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(254): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(163): Show |
1 | a0002c0003t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(161): Show |
1 | a0001c0001t0001g0005 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(170): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(313): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+242_1596+243i others(322): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | GGTGTGGA others(763): Show |
1 | a0001c0001t0001g0155 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1596+242_1596+243i others(772): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767711 | G | T | 7 | a0001c0001t0001g0108 a0002c0002t0002g0229 a0002c0002t0002g0299 others(4): Show |
7 | HG02300.hp2 HG02523.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+241G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767711 | |||||||
chr16:767711 | GGCGTGGA others(139): Show |
G | 1 | a0001c0001t0001g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1596+254_1596+399d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767711 | ||||||
chr16:767712 | G | GCGTGGAG others(7): Show |
1 | a0001c0001t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767712 | ||||||
chr16:767713 | C | A | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+243C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | |||||||
chr16:767713 | C | G | 3 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0003c0004t0003g0222 |
3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+243C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | |||||||
chr16:767713 | C | T | 13 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0150 others(10): Show |
13 | HG00558.hp1 HG02083.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+243C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767713 | |||||||
chr16:767714 | GT | G | 14 | a0001c0001t0001g0112 a0002c0003t0004g0211 a0002c0015t0003g0071 others(11): Show |
23 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+245delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767714 | |||||||
chr16:767715 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0008c0010t0002g0013 others(2): Show |
6 | HG01109.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+245T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767715 | |||||||
chr16:767715 | T | C | 3 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0003c0004t0003g0222 |
3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+245T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767715 | |||||||
chr16:767715 | TGGA | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0002c0002t0002g0229 others(4): Show |
7 | HG02523.hp2 NA18943.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+254_1596+256d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767715 | ||||||
chr16:767716 | G | C | 14 | a0001c0001t0001g0112 a0002c0003t0004g0211 a0002c0015t0003g0071 others(11): Show |
23 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+246G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767716 | |||||||
chr16:767716 | G | GC | 3 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0003c0004t0003g0222 |
3 | HG03225.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+246_1596+247i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767716 | |||||||
chr16:767717 | G | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+247G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767717 | |||||||
chr16:767718 | A | AGGAGGGG others(5): Show |
2 | a0005c0005t0001g0040 a0009c0012t0001g0325 |
2 | HG00738.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(4): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0154 a0019c0044t0001g0043 |
3 | HG00609.hp2 HG02145.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1596+250_1596+251i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(61): Show |
1 | a0001c0009t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(216): Show |
2 | a0004c0006t0001g0220 a0004c0020t0001g0287 |
2 | HG00558.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1596+250_1596+251i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(217): Show |
1 | a0004c0006t0001g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(226): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(27): Show |
1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1596+250_1596+251i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | AGGGGGGC others(53): Show |
1 | a0001c0039t0001g0147 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(62): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767718 | ||||||
chr16:767718 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+248A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767718 | |||||||
chr16:767718 | A | T | 18 | a0001c0001t0001g0112 a0002c0002t0002g0284 a0002c0003t0002g0247 others(15): Show |
27 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1596+248A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767718 | |||||||
chr16:767719 | G | GGGGGGCG others(149): Show |
1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(158): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767719 | ||||||
chr16:767720 | G | GGGGGCGC others(220): Show |
1 | a0001c0001t0001g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(229): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | |||||||
chr16:767720 | G | GGGGGCGC others(69): Show |
1 | a0001c0001t0001g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+250_1596+251i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | |||||||
chr16:767720 | GAGGA | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0003c0004t0003g0223 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+251_1596+254d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767720 | |||||||
chr16:767721 | A | AGGGGCGC others(2): Show |
10 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0122 others(7): Show |
10 | HG00280.hp2 HG00642.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+253_1596+254i others(11): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(100): Show |
1 | a0005c0005t0001g0036 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(85): Show |
1 | a0001c0001t0001g0326 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+253_1596+254i others(94): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(102): Show |
1 | a0001c0001t0001g0140 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(111): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(17): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0275 |
2 | HG01361.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(236): Show |
1 | a0001c0001t0001g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(245): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | AGGGGCGC others(33): Show |
1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767721 | ||||||
chr16:767721 | A | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0127 others(5): Show |
8 | HG01952.hp2 HG02683.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+251A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767721 | |||||||
chr16:767721 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596+251A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767721 | |||||||
chr16:767722 | G | GGGCGCGT others(3): Show |
1 | a0001c0001t0001g0090 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1596+253_1596+254i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | ||||||
chr16:767722 | G | GGGGCGCG others(4): Show |
10 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0119 others(7): Show |
10 | HG00609.hp1 HG02056.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+253_1596+254i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | ||||||
chr16:767722 | G | GGGGCGCG others(18): Show |
2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+253_1596+254i others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767722 | ||||||
chr16:767724 | A | G | 37 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0093 others(34): Show |
42 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1596+254A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767724 | |||||||
chr16:767725 | G | C | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+255G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767725 | |||||||
chr16:767727 | G | C | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+257G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767727 | |||||||
chr16:767728 | G | GGC | 14 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0122 others(11): Show |
14 | HG00280.hp2 HG00597.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+258_1596+259i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767728 | |||||||
chr16:767729 | C | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1596+259C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767729 | |||||||
chr16:767729 | C | T | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+259C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767729 | |||||||
chr16:767730 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+260G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767730 | |||||||
chr16:767731 | C | A | 4 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 others(1): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+261C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767731 | C | CGTGGAGG others(60): Show |
1 | a0019c0044t0001g0043 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1596+261_1596+262i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767731 | C | CGTGGAGG others(106): Show |
1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+261_1596+262i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767731 | C | G | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+261C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767731 | C | T | 28 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0088 others(25): Show |
33 | HG00280.hp2 HG00597.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1596+261C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767731 | CATGGGGG others(3): Show |
C | 2 | a0002c0002t0002g0284 a0002c0003t0002g0247 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+262_1596+271d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767731 | |||||||
chr16:767732 | A | G | 72 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0085 others(69): Show |
82 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1596+262A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767732 | |||||||
chr16:767733 | T | C | 4 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 others(1): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+263T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767733 | |||||||
chr16:767733 | T | G | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+263T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767733 | |||||||
chr16:767733 | T | TGGAGGGG others(85): Show |
1 | a0001c0001t0001g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1596+265_1596+266i others(94): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767733 | ||||||
chr16:767734 | G | GGAGGGGG others(6): Show |
1 | a0005c0005t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+265_1596+266i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767734 | ||||||
chr16:767736 | G | A | 1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1596+266G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767736 | |||||||
chr16:767737 | G | A | 4 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 others(1): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+267G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767737 | |||||||
chr16:767739 | G | C | 6 | a0001c0039t0001g0147 a0004c0006t0001g0220 a0004c0006t0001g0331 others(3): Show |
6 | HG00558.hp1 HG02155.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+269G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767739 | |||||||
chr16:767739 | G | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0001g0203 others(3): Show |
6 | HG02056.hp1 HG02486.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+269G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767739 | |||||||
chr16:767741 | T | C | 45 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0073 others(42): Show |
45 | HG00280.hp2 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1596+271T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767741 | |||||||
chr16:767741 | T | G | 2 | a0002c0003t0004g0208 a0002c0003t0004g0211 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+271T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767741 | |||||||
chr16:767741 | T | TGC | 10 | a0001c0001t0001g0090 a0001c0001t0001g0164 a0001c0001t0001g0237 others(7): Show |
15 | HG00639.hp1 HG01070.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596+272_1596+273i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | ||||||
chr16:767741 | T | TGTGGAGG others(71): Show |
1 | a0001c0001t0001g0061 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1596+283_1596+284i others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | ||||||
chr16:767741 | T | TGTGGAGG others(60): Show |
1 | a0005c0005t0001g0047 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1596+290_1596+356d others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | ||||||
chr16:767741 | T | TGTGGAGG others(99): Show |
2 | a0001c0001t0001g0110 a0001c0034t0001g0204 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1596+345_1596+346i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767741 | ||||||
chr16:767742 | G | C | 2 | a0002c0003t0004g0208 a0002c0003t0004g0211 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+272G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767742 | |||||||
chr16:767743 | T | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+273T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767743 | |||||||
chr16:767743 | T | C | 2 | a0002c0003t0004g0208 a0002c0003t0004g0211 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+273T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767743 | |||||||
chr16:767745 | G | C | 1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+275G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767745 | |||||||
chr16:767746 | A | AGGGGGGC others(122): Show |
1 | a0008c0010t0002g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | ||||||
chr16:767746 | A | AGGGGGGC others(135): Show |
1 | a0001c0001t0001g0096 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(144): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | ||||||
chr16:767746 | A | AGGGGGGT others(58): Show |
2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+282_1596+283i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767746 | ||||||
chr16:767746 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0177 a0001c0001t0001g0203 others(1): Show |
4 | HG02056.hp1 HG02300.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+276A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767746 | |||||||
chr16:767746 | A | T | 1 | a0002c0003t0004g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1596+276A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767746 | |||||||
chr16:767747 | G | GGGGGGCG others(329): Show |
1 | a0004c0006t0001g0261 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(338): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767747 | ||||||
chr16:767747 | G | T | 1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+277G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767747 | |||||||
chr16:767748 | G | A | 4 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 others(1): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+278G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | |||||||
chr16:767748 | G | GA | 20 | a0001c0001t0001g0090 a0001c0001t0001g0164 a0001c0001t0001g0237 others(17): Show |
25 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+278_1596+279i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | |||||||
chr16:767748 | G | GGGGCACG others(48): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0203 |
2 | HG02056.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1596+281_1596+282i others(57): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCAC others(49): Show |
1 | a0001c0001t0001g0177 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1596+283_1596+284i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(125): Show |
1 | a0005c0005t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+295_1596+296i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(289): Show |
1 | a0001c0001t0001g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+299_1596+300i others(298): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(165): Show |
1 | a0001c0001t0001g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(174): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(162): Show |
1 | a0009c0012t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(189): Show |
1 | a0001c0001t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(198): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(361): Show |
1 | a0004c0016t0001g0139 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(370): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(136): Show |
1 | a0001c0001t0001g0130 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(190): Show |
1 | a0001c0009t0001g0292 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(199): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(136): Show |
2 | a0008c0010t0002g0013 a0008c0010t0002g0055 |
3 | HG01891.hp2 HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(137): Show |
1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(137): Show |
2 | a0006c0008t0001g0023 a0006c0008t0001g0252 |
3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(146): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(136): Show |
1 | a0001c0001t0001g0159 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(145): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(400): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(409): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(162): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(171): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(198): Show |
1 | a0001c0001t0001g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(57): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0131 |
2 | HG00597.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1596+289_1596+290i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGCGC others(72): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0170 |
2 | NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1596+289_1596+290i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | GGGGGTGC others(8): Show |
1 | a0001c0001t0001g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+282_1596+283i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767748 | G | T | 1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1596+278G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767748 | |||||||
chr16:767748 | GGGGGCGC others(8): Show |
G | 5 | a0001c0001t0001g0065 a0002c0002t0002g0283 a0002c0002t0002g0315 others(2): Show |
5 | HG02074.hp2 HG02080.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+293_1596+307d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767748 | ||||||
chr16:767749 | G | GGGGCGCG others(50): Show |
1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767749 | ||||||
chr16:767751 | G | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0007c0007t0001g0052 others(1): Show |
5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+281G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767751 | |||||||
chr16:767752 | G | GCGCGTGG others(19): Show |
1 | a0002c0003t0004g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1596+295_1596+296i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(19): Show |
32 | a0001c0001t0001g0105 a0001c0001t0001g0113 a0001c0001t0001g0118 others(29): Show |
33 | HG00558.hp2 HG00738.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(115): Show |
4 | a0002c0002t0002g0186 a0002c0002t0002g0307 a0002c0002t0002g0308 others(1): Show |
4 | HG00733.hp2 NA18940.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(274): Show |
1 | a0002c0002t0002g0309 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(283): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(159): Show |
1 | a0002c0003t0004g0228 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(168): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(20): Show |
1 | a0001c0001t0001g0114 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767752 | G | GCGCGTGG others(6): Show |
1 | a0005c0043t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767752 | ||||||
chr16:767753 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0007c0007t0001g0052 others(1): Show |
5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+283C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | |||||||
chr16:767753 | C | CGCGTGGA others(96): Show |
1 | a0001c0001t0001g0238 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(105): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGA others(132): Show |
1 | a0001c0001t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(141): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGA others(121): Show |
1 | a0002c0003t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGA others(121): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGA others(43): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGA others(108): Show |
1 | a0004c0016t0001g0257 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(117): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGG others(390): Show |
1 | a0001c0001t0001g0324 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGG others(42): Show |
1 | a0005c0005t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+289_1596+290i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGG others(219): Show |
1 | a0001c0001t0001g0093 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+289_1596+290i others(228): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | CGCGTGGG others(230): Show |
1 | a0009c0012t0001g0325 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1596+289_1596+290i others(239): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767753 | ||||||
chr16:767753 | C | G | 2 | a0002c0003t0004g0208 a0002c0003t0004g0211 |
2 | HG02293.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1596+283C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | |||||||
chr16:767753 | C | T | 6 | a0001c0001t0001g0101 a0001c0001t0001g0135 a0001c0001t0001g0218 others(3): Show |
6 | HG01099.hp1 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+283C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767753 | |||||||
chr16:767754 | G | A | 4 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 others(1): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+284G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767754 | |||||||
chr16:767754 | G | GCGTGGAG others(6): Show |
3 | a0001c0001t0001g0104 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | NA18952.hp1 NA19010.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1596+292_1596+293i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767754 | ||||||
chr16:767755 | C | A | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+285C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767755 | |||||||
chr16:767755 | C | CGTGGAGG others(18): Show |
1 | a0002c0003t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+287_1596+311d others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | ||||||
chr16:767755 | C | CGTGGAGG others(75): Show |
1 | a0002c0003t0002g0262 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | ||||||
chr16:767755 | C | CGTGGAGG others(19): Show |
1 | a0004c0020t0001g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767755 | ||||||
chr16:767756 | G | A | 1 | a0002c0003t0004g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+286G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767756 | |||||||
chr16:767756 | G | GTGGAGGG others(63): Show |
1 | a0001c0001t0001g0274 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(72): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767756 | ||||||
chr16:767756 | GT | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0007c0007t0001g0052 others(1): Show |
5 | HG01109.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+287delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767756 | |||||||
chr16:767757 | T | TGGA | 3 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 |
3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+293_1596+295d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767757 | ||||||
chr16:767757 | TGGAGGAG others(50): Show |
T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1596+290_1596+346d others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767757 | ||||||
chr16:767760 | A | AGGGGGCA others(3): Show |
5 | a0002c0002t0002g0027 a0002c0002t0002g0056 a0002c0002t0002g0321 others(2): Show |
5 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | ||||||
chr16:767760 | A | AGGGGGCA others(176): Show |
1 | a0002c0002t0002g0190 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(185): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | ||||||
chr16:767760 | A | AGGGGGCA others(81): Show |
1 | a0008c0010t0002g0251 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(90): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | ||||||
chr16:767760 | A | AGGGGGGC others(40): Show |
1 | a0014c0023t0002g0037 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767760 | ||||||
chr16:767760 | A | G | 3 | a0001c0001t0001g0160 a0003c0004t0003g0222 a0005c0005t0001g0034 |
3 | HG02886.hp2 NA19089.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+290A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767760 | |||||||
chr16:767760 | A | T | 2 | a0002c0003t0004g0210 a0004c0006t0001g0335 |
2 | HG01978.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1596+290A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767760 | |||||||
chr16:767761 | G | GGGGGCAC others(99): Show |
1 | a0002c0002t0002g0296 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1596+292_1596+293i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | ||||||
chr16:767761 | G | GGGGGCAC others(74): Show |
24 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0060 others(21): Show |
32 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | ||||||
chr16:767761 | G | GGGGGCAC others(88): Show |
1 | a0002c0002t0002g0312 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | ||||||
chr16:767761 | G | GGGGGCAC others(44): Show |
3 | a0002c0002t0002g0026 a0002c0002t0002g0313 a0002c0002t0002g0314 |
4 | HG01069.hp1 HG01192.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | ||||||
chr16:767761 | GGA | G | 22 | a0001c0001t0001g0076 a0001c0001t0001g0219 a0001c0021t0001g0264 others(19): Show |
27 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1596+293_1596+294d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767761 | ||||||
chr16:767762 | G | GGGGCACG others(60): Show |
1 | a0002c0002t0002g0278 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1596+292_1596+293i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | |||||||
chr16:767762 | G | GGGGCGCG others(4): Show |
4 | a0002c0003t0004g0214 a0002c0003t0004g0215 a0002c0015t0003g0249 others(1): Show |
4 | HG02109.hp1 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+292_1596+293i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | |||||||
chr16:767762 | GA | G | 3 | a0002c0002t0002g0010 a0002c0002t0002g0301 a0003c0004t0003g0269 |
5 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+293delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767762 | |||||||
chr16:767763 | A | AGGAGGGG others(20): Show |
3 | a0001c0001t0001g0061 a0001c0001t0001g0112 a0001c0001t0001g0162 |
3 | HG01169.hp1 HG03490.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1596+295_1596+296i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767763 | A | AGGCACGT others(79): Show |
1 | a0002c0003t0004g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1596+295_1596+296i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767763 | A | AGGGGCGC others(7): Show |
1 | a0001c0001t0001g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1596+298_1596+311d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767763 | A | AGGGGCGC others(409): Show |
1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(418): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767763 | A | AGGGGCGC others(8): Show |
1 | a0005c0005t0009g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596+297_1596+311d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767763 | A | G | 49 | a0001c0001t0001g0160 a0001c0001t0001g0333 a0001c0001t0001g0334 others(46): Show |
58 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1596+293A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767763 | |||||||
chr16:767763 | AGGGGCGC others(58): Show |
A | 1 | a0012c0017t0001g0184 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1596+301_1596+365d others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767763 | ||||||
chr16:767767 | G | GT | 5 | a0002c0002t0002g0027 a0002c0002t0002g0056 a0002c0002t0002g0321 others(2): Show |
5 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+297_1596+298i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767767 | |||||||
chr16:767768 | C | CGCGTGGA others(21): Show |
1 | a0002c0003t0001g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1596+307_1596+308i others(30): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767768 | ||||||
chr16:767768 | C | G | 2 | a0002c0002t0002g0278 a0029c0042t0002g0244 |
2 | HG04199.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1596+298C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767768 | |||||||
chr16:767768 | C | T | 1 | a0004c0006t0001g0220 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1596+298C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767768 | |||||||
chr16:767769 | G | A | 20 | a0001c0001t0001g0076 a0001c0001t0001g0160 a0001c0001t0001g0219 others(17): Show |
21 | HG01361.hp1 HG01981.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1596+299G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767769 | |||||||
chr16:767769 | GCGTGGA | G | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+300_1596+305d others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767769 | |||||||
chr16:767770 | C | A | 4 | a0002c0003t0004g0227 a0007c0007t0001g0007 a0007c0007t0001g0239 others(1): Show |
6 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+300C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767770 | |||||||
chr16:767770 | C | T | 5 | a0002c0002t0002g0278 a0003c0004t0003g0223 a0003c0004t0003g0266 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+300C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767770 | |||||||
chr16:767771 | G | A | 3 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 |
3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+301G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767771 | |||||||
chr16:767771 | G | GC | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+301_1596+302i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767771 | |||||||
chr16:767772 | T | G | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+302T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767772 | |||||||
chr16:767775 | A | G | 5 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 others(2): Show |
5 | HG02027.hp1 HG02818.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+305A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767775 | |||||||
chr16:767775 | AG | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0145 a0002c0002t0002g0229 others(5): Show |
8 | HG00408.hp1 HG00733.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+311delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767775 | ||||||
chr16:767775 | AGGGGGGA others(69): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1596+311_1596+386d others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767775 | ||||||
chr16:767776 | G | A | 3 | a0002c0003t0004g0208 a0002c0003t0004g0211 a0013c0018t0001g0009 |
5 | HG02293.hp2 HG02300.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+306G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767776 | |||||||
chr16:767776 | GGGGGGAG others(3): Show |
G | 15 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0219 others(12): Show |
17 | HG01109.hp2 HG01361.hp1 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596+312_1596+321d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767776 | ||||||
chr16:767777 | G | GA | 10 | a0002c0002t0002g0010 a0002c0002t0002g0027 a0002c0002t0002g0056 others(7): Show |
14 | HG00099.hp2 HG02004.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596+307_1596+308i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767777 | |||||||
chr16:767777 | G | GAGGA | 6 | a0004c0006t0001g0220 a0004c0006t0001g0261 a0004c0006t0001g0331 others(3): Show |
6 | HG00558.hp1 HG00642.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+307_1596+308i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767777 | |||||||
chr16:767778 | G | A | 3 | a0002c0002t0002g0284 a0002c0003t0002g0247 a0007c0007t0001g0052 |
3 | HG02280.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+308G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767778 | |||||||
chr16:767778 | G | C | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+308G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767778 | |||||||
chr16:767778 | G | GGTCGCGT others(280): Show |
1 | a0004c0016t0001g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1596+309_1596+310i others(289): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767778 | ||||||
chr16:767779 | G | GGGGCGAG others(4): Show |
1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+311_1596+312i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767779 | ||||||
chr16:767779 | G | GT | 3 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 |
3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+309_1596+310i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767779 | |||||||
chr16:767779 | G | GTCGCGT | 12 | a0002c0002t0002g0316 a0002c0015t0003g0249 a0002c0015t0003g0250 others(9): Show |
16 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+309_1596+310i others(8): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767779 | |||||||
chr16:767781 | G | C | 54 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(51): Show |
66 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1596+311G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | |||||||
chr16:767781 | G | GGCGTGTG others(8): Show |
1 | a0002c0003t0004g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1596+311_1596+312i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | |||||||
chr16:767781 | G | T | 3 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 |
3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+311G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | |||||||
chr16:767781 | GA | G | 3 | a0002c0002t0002g0190 a0003c0004t0003g0222 a0008c0010t0002g0251 |
3 | HG03209.hp2 NA18941.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+312delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767781 | |||||||
chr16:767782 | A | C | 91 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0095 others(88): Show |
97 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1596+312A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | |||||||
chr16:767782 | A | G | 6 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 others(3): Show |
6 | HG01978.hp1 HG02027.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+312A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | |||||||
chr16:767782 | A | T | 4 | a0003c0004t0003g0280 a0007c0007t0001g0007 a0007c0007t0001g0239 others(1): Show |
6 | HG02055.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+312A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | |||||||
chr16:767782 | AG | A | 34 | a0001c0001t0001g0112 a0002c0002t0002g0001 a0002c0002t0002g0025 others(31): Show |
43 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1596+313delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767782 | |||||||
chr16:767782 | AGCGTGGG others(31): Show |
A | 1 | a0001c0001t0001g0153 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1596+323_1596+360d others(40): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767782 | ||||||
chr16:767783 | G | A | 2 | a0002c0002t0002g0187 a0029c0042t0002g0244 |
2 | NA18990.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1596+313G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767783 | |||||||
chr16:767783 | GC | G | 16 | a0002c0002t0002g0316 a0002c0015t0003g0249 a0002c0015t0003g0250 others(13): Show |
22 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+314delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767783 | |||||||
chr16:767784 | C | A | 3 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 |
3 | HG02027.hp1 NA18999.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1596+314C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767784 | |||||||
chr16:767784 | C | T | 17 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(14): Show |
19 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+314C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767784 | |||||||
chr16:767785 | G | A | 4 | a0004c0006t0001g0220 a0004c0020t0001g0287 a0015c0022t0001g0029 others(1): Show |
4 | HG00558.hp1 HG01099.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+315G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767785 | |||||||
chr16:767786 | T | A | 19 | a0002c0002t0002g0284 a0002c0002t0002g0316 a0002c0003t0002g0247 others(16): Show |
25 | HG01106.hp2 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+316T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767786 | |||||||
chr16:767786 | T | G | 5 | a0001c0001t0010g0137 a0001c0009t0001g0291 a0001c0009t0001g0293 others(2): Show |
5 | HG00642.hp1 HG02027.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+316T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767786 | |||||||
chr16:767786 | T | TG | 48 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0104 others(45): Show |
56 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1596+322dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGAGGGG others(8): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+318_1596+319i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(7): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(310): Show |
1 | a0001c0009t0001g0289 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(319): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(111): Show |
1 | a0002c0003t0002g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(109): Show |
1 | a0002c0003t0004g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(118): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(70): Show |
1 | a0001c0001t0001g0246 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(79): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGGG others(221): Show |
1 | a0001c0001t0001g0273 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(230): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGGGGGTG others(19): Show |
1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+321_1596+322i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767786 | T | TGTGGGGG others(9): Show |
1 | a0002c0003t0004g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1596+317_1596+318i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767786 | ||||||
chr16:767787 | G | GGA | 10 | a0002c0002t0002g0027 a0002c0002t0002g0229 a0002c0002t0002g0299 others(7): Show |
10 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+318_1596+319i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767787 | ||||||
chr16:767789 | G | A | 41 | a0001c0001t0001g0112 a0002c0002t0002g0001 a0002c0002t0002g0025 others(38): Show |
52 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1596+319G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767789 | |||||||
chr16:767789 | G | C | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+319G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767789 | |||||||
chr16:767790 | G | A | 6 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(3): Show |
6 | HG02155.hp2 HG02523.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+320G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | |||||||
chr16:767790 | G | C | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+320G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | |||||||
chr16:767790 | G | T | 12 | a0001c0001t0001g0219 a0001c0021t0001g0264 a0002c0002t0002g0059 others(9): Show |
13 | HG01361.hp1 HG01981.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+320G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767790 | |||||||
chr16:767791 | G | A | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+321G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | |||||||
chr16:767791 | G | C | 36 | a0001c0001t0001g0219 a0001c0001t0010g0137 a0001c0009t0001g0291 others(33): Show |
43 | HG01106.hp2 HG01361.hp1 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.1596+321G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | |||||||
chr16:767791 | G | GGCGTGGA others(442): Show |
1 | a0001c0001t0001g0117 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(451): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGCGTGGA others(88): Show |
2 | a0001c0001t0001g0177 a0001c0009t0001g0292 |
2 | HG02040.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1596+348_1596+349i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGCGTGGA others(89): Show |
1 | a0001c0001t0001g0108 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(98): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGCGTGGA others(142): Show |
1 | a0001c0001t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1596+349_1597-412d others(151): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGCGAGT others(74): Show |
1 | a0014c0023t0013g0279 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(83): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGCGCAT others(34): Show |
1 | a0002c0003t0004g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(43): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGGCGCA others(22): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGGCGCG others(78): Show |
1 | a0002c0002t0002g0056 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(87): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGGGCGC others(105): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(114): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGGGCGC others(283): Show |
1 | a0001c0001t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(292): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTC | 36 | a0001c0001t0001g0112 a0002c0002t0002g0001 a0002c0002t0002g0025 others(33): Show |
45 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1596+322_1596+323i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGCGT others(121): Show |
1 | a0001c0001t0001g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(83): Show |
1 | a0002c0003t0004g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(125): Show |
1 | a0002c0002t0002g0297 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(82): Show |
1 | a0002c0002t0002g0309 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(91): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(126): Show |
1 | a0002c0002t0002g0186 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(135): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(125): Show |
2 | a0002c0002t0002g0307 a0002c0002t0002g0308 |
2 | NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(134): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(84): Show |
2 | a0002c0003t0004g0021 a0002c0003t0004g0228 |
3 | HG02818.hp1 HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(123): Show |
1 | a0002c0003t0004g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(173): Show |
1 | a0002c0003t0004g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(182): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(216): Show |
1 | a0008c0010t0002g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(204): Show |
1 | a0005c0043t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(213): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(235): Show |
3 | a0001c0021t0001g0175 a0004c0006t0001g0245 a0030c0031t0001g0176 |
3 | HG03669.hp1 HG04204.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1596+322_1596+323i others(244): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(266): Show |
1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(275): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(312): Show |
1 | a0027c0032t0001g0327 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(321): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(296): Show |
1 | a0004c0006t0001g0255 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1596+322_1596+323i others(305): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(58): Show |
1 | a0006c0008t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(67): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GGGTGTGG others(248): Show |
1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1596+322_1596+323i others(257): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767791 | ||||||
chr16:767791 | G | GTGCGTGG others(227): Show |
3 | a0006c0008t0001g0011 a0006c0008t0001g0032 a0026c0041t0001g0011 |
3 | HG02451.hp2 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1596+321_1596+322i others(236): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | |||||||
chr16:767791 | G | GTGCGTGG others(228): Show |
1 | a0006c0008t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596+321_1596+322i others(237): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | |||||||
chr16:767791 | G | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0003c0004t0003g0222 others(7): Show |
14 | HG01109.hp2 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+321G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767791 | |||||||
chr16:767793 | C | A | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+323C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | |||||||
chr16:767793 | C | CGCGTG | 4 | a0002c0002t0002g0027 a0002c0002t0002g0321 a0002c0002t0012g0027 others(1): Show |
4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+324_1596+325i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767793 | ||||||
chr16:767793 | C | G | 5 | a0002c0002t0002g0322 a0003c0004t0003g0265 a0007c0007t0001g0007 others(2): Show |
7 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+323C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | |||||||
chr16:767793 | C | T | 16 | a0001c0001t0001g0273 a0001c0009t0001g0289 a0002c0003t0002g0241 others(13): Show |
16 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1596+323C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767793 | |||||||
chr16:767794 | G | A | 2 | a0002c0002t0002g0284 a0002c0003t0002g0247 |
2 | HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+324G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767794 | |||||||
chr16:767794 | G | GCGTGGAG others(175): Show |
1 | a0002c0002t0002g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1596+324_1596+325i others(184): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767794 | |||||||
chr16:767795 | T | A | 4 | a0002c0002t0002g0027 a0002c0002t0002g0321 a0002c0002t0012g0027 others(1): Show |
4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+325T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | |||||||
chr16:767795 | T | C | 1 | a0002c0002t0002g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+325T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | |||||||
chr16:767795 | T | G | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+325T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767795 | |||||||
chr16:767796 | G | GC | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+326_1596+327i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767796 | |||||||
chr16:767797 | G | C | 1 | a0002c0002t0002g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+327G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767797 | |||||||
chr16:767798 | A | C | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+328A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | |||||||
chr16:767798 | A | T | 4 | a0001c0001t0001g0095 a0007c0007t0001g0007 a0007c0007t0001g0239 others(1): Show |
6 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+328A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | |||||||
chr16:767798 | AGG | A | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+329_1596+330d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767798 | |||||||
chr16:767799 | G | T | 1 | a0002c0002t0002g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+329G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767799 | |||||||
chr16:767800 | G | C | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+330G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767800 | |||||||
chr16:767800 | GA | G | 18 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0001g0219 others(15): Show |
18 | HG00423.hp2 HG00558.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+331delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767800 | |||||||
chr16:767801 | A | AGGGGCGC others(129): Show |
1 | a0022c0036t0001g0126 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1596+348_1596+349i others(138): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767801 | ||||||
chr16:767801 | A | AGGGGGCG others(75): Show |
1 | a0001c0001t0001g0324 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1596+335_1596+336i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767801 | ||||||
chr16:767801 | A | ATG | 5 | a0002c0002t0002g0229 a0002c0002t0002g0299 a0002c0002t0002g0300 others(2): Show |
5 | HG02155.hp2 HG02523.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+331_1596+332i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | |||||||
chr16:767801 | A | C | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+331A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | |||||||
chr16:767801 | A | G | 17 | a0001c0001t0001g0068 a0001c0001t0001g0095 a0001c0001t0001g0273 others(14): Show |
18 | HG00423.hp1 HG02132.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+331A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767801 | |||||||
chr16:767806 | C | CGCGTGGA others(731): Show |
1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1596+345_1596+346i others(740): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | ||||||
chr16:767806 | C | CGCGTGGA others(17): Show |
1 | a0001c0001t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1596+348_1596+349i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | ||||||
chr16:767806 | C | CGCGTGGA others(195): Show |
1 | a0023c0040t0001g0168 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(204): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | ||||||
chr16:767806 | C | CGCGTGGA others(30): Show |
1 | a0005c0005t0001g0044 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1596+362_1596+363i others(39): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767806 | ||||||
chr16:767806 | C | G | 8 | a0002c0002t0002g0229 a0002c0002t0002g0284 a0002c0002t0002g0299 others(5): Show |
8 | HG02155.hp2 HG02523.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+336C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767806 | |||||||
chr16:767806 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0161 a0002c0003t0004g0227 others(1): Show |
6 | HG02451.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+336C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767806 | |||||||
chr16:767808 | C | A | 5 | a0002c0003t0004g0209 a0006c0008t0001g0011 a0006c0008t0001g0032 others(2): Show |
5 | HG01943.hp2 HG02451.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+338C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | |||||||
chr16:767808 | C | CATGGGGG others(3): Show |
4 | a0002c0002t0002g0027 a0002c0002t0002g0321 a0002c0002t0012g0027 others(1): Show |
4 | HG00099.hp2 HG02004.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+338_1596+339i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | |||||||
chr16:767808 | C | CGTGGAGG others(98): Show |
1 | a0001c0001t0001g0073 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | ||||||
chr16:767808 | C | CGTGGAGG others(8): Show |
1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1596+349_1596+350i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | ||||||
chr16:767808 | C | CGTGGAGG others(23): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1596+349_1596+350i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | ||||||
chr16:767808 | C | CGTGGAGG others(192): Show |
1 | a0008c0010t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1596+349_1596+350i others(201): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | ||||||
chr16:767808 | C | CGTGGGGG others(3): Show |
1 | a0004c0006t0001g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1596+342_1596+343i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767808 | ||||||
chr16:767808 | C | T | 16 | a0001c0001t0001g0088 a0001c0001t0001g0152 a0001c0001t0001g0202 others(13): Show |
18 | HG00140.hp1 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+338C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767808 | |||||||
chr16:767809 | G | A | 2 | a0002c0003t0002g0241 a0002c0003t0002g0243 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1596+339G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767809 | |||||||
chr16:767810 | T | C | 1 | a0006c0008t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+340T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767810 | |||||||
chr16:767810 | TGGAG | T | 5 | a0001c0001t0001g0219 a0003c0004t0003g0263 a0004c0006t0001g0234 others(2): Show |
5 | HG00423.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+343_1596+346d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767810 | ||||||
chr16:767812 | G | GGGGTGCG others(1): Show |
4 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0004c0006t0001g0179 others(1): Show |
4 | HG02080.hp2 HG02647.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+342_1596+343i others(10): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767812 | |||||||
chr16:767813 | A | AG | 14 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0166 others(11): Show |
15 | HG00408.hp1 HG01169.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596+349dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | ||||||
chr16:767813 | A | AGGGGGGG others(166): Show |
1 | a0009c0012t0001g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1596+349_1596+350i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | ||||||
chr16:767813 | A | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0002c0003t0002g0241 others(7): Show |
13 | HG01109.hp2 HG02055.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+343A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767813 | |||||||
chr16:767813 | AG | A | 6 | a0002c0002t0002g0191 a0002c0002t0002g0283 a0002c0002t0002g0310 others(3): Show |
6 | HG00733.hp2 HG02080.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+349delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767813 | ||||||
chr16:767815 | G | C | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+345G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | |||||||
chr16:767815 | G | GA | 19 | a0001c0001t0001g0161 a0003c0004t0003g0002 a0003c0004t0003g0222 others(16): Show |
23 | HG00558.hp1 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+345_1596+346i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | |||||||
chr16:767815 | G | GAGGA | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0008g0144 others(2): Show |
7 | HG00423.hp1 HG01192.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+345_1596+346i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | |||||||
chr16:767815 | G | GAGGGGCG others(69): Show |
1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+345_1596+346i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | |||||||
chr16:767815 | G | GAGGGGCG others(171): Show |
1 | a0004c0006t0001g0335 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596+345_1596+346i others(180): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767815 | |||||||
chr16:767815 | G | GGGGCCGT others(75): Show |
1 | a0009c0012t0001g0325 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1596+348_1596+349i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | ||||||
chr16:767815 | G | GGGGCGCG others(7): Show |
6 | a0001c0021t0001g0175 a0004c0006t0001g0183 a0004c0006t0001g0256 others(3): Show |
6 | HG03669.hp1 HG04184.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+348_1596+349i others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | ||||||
chr16:767815 | G | GGGGGCGC others(50): Show |
1 | a0001c0001t0001g0017 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | ||||||
chr16:767815 | G | GGGGGCGC others(189): Show |
1 | a0001c0001t0001g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(198): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767815 | ||||||
chr16:767818 | G | A | 3 | a0007c0007t0001g0007 a0007c0007t0001g0239 a0007c0007t0001g0240 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+348G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767818 | |||||||
chr16:767819 | G | C | 23 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0070 others(20): Show |
24 | HG00597.hp1 HG00597.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+349G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767819 | |||||||
chr16:767820 | C | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0080 a0001c0001t0001g0324 others(10): Show |
13 | HG02040.hp1 HG02486.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+350C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767820 | |||||||
chr16:767820 | C | CGCGTGGG others(288): Show |
1 | a0001c0001t0001g0180 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596+372_1596+373i others(297): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767820 | ||||||
chr16:767820 | C | T | 9 | a0001c0001t0001g0092 a0001c0001t0001g0219 a0002c0002t0002g0316 others(6): Show |
9 | HG00423.hp2 HG02132.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+350C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767820 | |||||||
chr16:767821 | G | A | 2 | a0004c0006t0001g0179 a0004c0006t0001g0260 |
2 | HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596+351G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767821 | |||||||
chr16:767822 | C | CGTGGGGG others(28): Show |
1 | a0001c0001t0001g0146 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | ||||||
chr16:767822 | C | CGTGGGGG others(27): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | ||||||
chr16:767822 | C | CGTGGGGG others(3): Show |
1 | a0001c0001t0001g0104 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1596+359_1596+360i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767822 | ||||||
chr16:767822 | C | T | 24 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0070 others(21): Show |
25 | HG00597.hp1 HG00597.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.1596+352C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767822 | |||||||
chr16:767823 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0008g0144 others(2): Show |
7 | HG00423.hp1 HG01192.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+353G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767823 | |||||||
chr16:767823 | GTGGGGGG others(6): Show |
G | 2 | a0002c0003t0004g0214 a0002c0003t0004g0215 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1596+362_1596+374d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767823 | ||||||
chr16:767824 | T | G | 1 | a0002c0002t0002g0316 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596+354T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767824 | |||||||
chr16:767824 | T | TGGGGGGG others(163): Show |
1 | a0001c0001t0001g0339 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1596+362_1596+363i others(172): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767824 | ||||||
chr16:767825 | G | A | 2 | a0001c0001t0001g0106 a0002c0002t0002g0316 |
2 | HG00099.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1596+355G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767825 | |||||||
chr16:767825 | G | GGAGGA | 19 | a0001c0001t0001g0161 a0001c0021t0001g0175 a0002c0002t0002g0191 others(16): Show |
19 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+356_1596+357i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGAGGAGG others(255): Show |
1 | a0016c0027t0001g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(264): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGAGGAGG others(71): Show |
1 | a0004c0006t0001g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1596+356_1596+357i others(80): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGAGGGGG others(112): Show |
1 | a0008c0010t0002g0013 | 2 | HG01891.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGAGGGGG others(115): Show |
1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGAGGGGG others(57): Show |
1 | a0008c0010t0002g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1596+356_1596+357i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767825 | G | GGGGGGGT others(26): Show |
1 | a0029c0042t0002g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(35): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767825 | ||||||
chr16:767826 | G | GA | 27 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0333 others(24): Show |
37 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1596+356_1596+357i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767826 | |||||||
chr16:767826 | G | GAGGGGGG others(9): Show |
3 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0016c0028t0001g0221 |
3 | HG01884.hp1 HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1596+356_1596+357i others(18): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767826 | |||||||
chr16:767826 | G | GGGGGGCG others(4): Show |
1 | a0001c0039t0001g0147 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | ||||||
chr16:767826 | G | GGGGGGGT others(5): Show |
4 | a0001c0021t0001g0264 a0002c0002t0002g0195 a0002c0015t0003g0249 others(1): Show |
4 | HG01361.hp1 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+362_1596+363i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | ||||||
chr16:767826 | G | GGGGGGGT others(29): Show |
1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1596+362_1596+363i others(38): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | ||||||
chr16:767826 | G | GGGGGGTG others(4): Show |
37 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0026 others(34): Show |
46 | HG00621.hp1 HG00621.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | ||||||
chr16:767826 | G | GGGGGGTG others(28): Show |
2 | a0003c0004t0003g0028 a0003c0004t0003g0337 |
3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767826 | ||||||
chr16:767827 | G | A | 15 | a0002c0002t0002g0027 a0002c0002t0002g0229 a0002c0002t0002g0284 others(12): Show |
16 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.1596+357G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767827 | |||||||
chr16:767827 | G | GGGGGTGT others(3): Show |
2 | a0002c0002t0002g0294 a0002c0002t0002g0323 |
2 | NA18953.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | ||||||
chr16:767827 | G | GGGGGTGT others(14): Show |
1 | a0002c0002t0002g0307 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(23): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | ||||||
chr16:767827 | G | GGGGGTGT others(188): Show |
1 | a0002c0002t0002g0304 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(197): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767827 | ||||||
chr16:767828 | G | A | 23 | a0001c0001t0001g0106 a0001c0001t0001g0161 a0001c0021t0001g0175 others(20): Show |
23 | HG00099.hp1 HG00558.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596+358G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767828 | |||||||
chr16:767828 | G | GGGGCGTG others(5): Show |
2 | a0001c0001t0001g0326 a0004c0016t0001g0257 |
2 | HG00597.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(23): Show |
1 | a0001c0001t0001g0093 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(175): Show |
1 | a0001c0001t0001g0066 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(184): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(22): Show |
7 | a0001c0001t0001g0090 a0001c0001t0001g0109 a0001c0001t0001g0130 others(4): Show |
7 | HG02056.hp1 HG02155.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(250): Show |
1 | a0001c0001t0001g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(259): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(117): Show |
1 | a0001c0001t0001g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(126): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(201): Show |
1 | a0001c0001t0001g0091 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(210): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(79): Show |
1 | a0005c0005t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(292): Show |
1 | a0009c0012t0001g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(301): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(124): Show |
1 | a0001c0001t0001g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(133): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGCGTG others(79): Show |
1 | a0001c0001t0008g0144 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGTGTG others(37): Show |
1 | a0001c0001t0001g0067 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGTGTG others(75): Show |
1 | a0001c0001t0001g0068 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1596+361_1596+362i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGTGTG others(76): Show |
1 | a0002c0002t0002g0010 | 3 | HG02922.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(85): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGGTGTG others(154): Show |
1 | a0001c0001t0001g0118 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596+361_1596+362i others(163): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGGTGTGG others(46): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1596+360_1596+361i others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767828 | G | GGTGCGTG others(278): Show |
1 | a0004c0006t0001g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1596+359_1596+360i others(287): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767828 | ||||||
chr16:767830 | GGGCGCAT others(35): Show |
G | 1 | a0006c0011t0001g0233 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1596+362_1596+403d others(44): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767830 | ||||||
chr16:767831 | G | C | 2 | a0001c0001t0001g0080 a0005c0005t0001g0034 |
2 | HG03492.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+361G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | |||||||
chr16:767831 | G | GA | 1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | |||||||
chr16:767831 | G | GC | 8 | a0001c0001t0001g0113 a0001c0001t0001g0246 a0002c0003t0001g0099 others(5): Show |
9 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | |||||||
chr16:767831 | G | GT | 6 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0006c0011t0001g0022 others(3): Show |
7 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+361_1596+362i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | |||||||
chr16:767831 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+361G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767831 | |||||||
chr16:767832 | G | C | 9 | a0005c0005t0001g0012 a0005c0005t0001g0031 a0005c0005t0001g0040 others(6): Show |
11 | HG00738.hp2 HG01243.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+362G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767832 | |||||||
chr16:767833 | C | A | 3 | a0002c0003t0004g0227 a0003c0004t0003g0222 a0009c0012t0001g0325 |
3 | HG03130.hp2 NA19083.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1596+363C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767833 | |||||||
chr16:767833 | C | T | 29 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0112 others(26): Show |
31 | HG00609.hp2 HG00639.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1596+363C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767833 | |||||||
chr16:767834 | G | A | 24 | a0001c0001t0001g0005 a0001c0001t0001g0092 a0001c0001t0001g0104 others(21): Show |
24 | HG00099.hp2 HG00558.hp2 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.1596+364G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767834 | |||||||
chr16:767835 | C | G | 20 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0112 others(17): Show |
22 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596+365C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767835 | |||||||
chr16:767835 | C | T | 8 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0002c0033t0003g0253 others(5): Show |
9 | HG00738.hp2 HG02080.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+365C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767835 | |||||||
chr16:767836 | A | G | 73 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0092 others(70): Show |
86 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1596+366A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767836 | |||||||
chr16:767837 | T | G | 22 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0112 others(19): Show |
25 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+367T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767837 | |||||||
chr16:767837 | T | TG | 33 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0062 others(30): Show |
35 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.1596+374dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | ||||||
chr16:767837 | T | TGGA | 10 | a0001c0001t0001g0092 a0003c0004t0003g0028 a0003c0004t0003g0263 others(7): Show |
11 | HG00423.hp2 HG01884.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | ||||||
chr16:767837 | T | TGGGGGTG others(4): Show |
1 | a0002c0002t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1596+372_1596+373i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | ||||||
chr16:767837 | T | TGGGGGTG others(5): Show |
4 | a0002c0002t0002g0194 a0002c0002t0002g0318 a0002c0002t0002g0328 others(1): Show |
4 | HG00621.hp1 HG00621.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+372_1596+373i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767837 | ||||||
chr16:767838 | G | GA | 7 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0246 others(4): Show |
7 | HG00738.hp1 HG01257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+368_1596+369i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767838 | |||||||
chr16:767838 | G | GGAGGA | 7 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0326 others(4): Show |
8 | HG00597.hp2 HG01109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(7): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767838 | ||||||
chr16:767839 | G | GA | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+369_1596+370i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767839 | |||||||
chr16:767840 | G | A | 13 | a0002c0002t0002g0027 a0002c0002t0002g0229 a0002c0002t0002g0284 others(10): Show |
13 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596+370G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767840 | |||||||
chr16:767841 | G | C | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+371G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767841 | |||||||
chr16:767843 | G | A | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+373G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | |||||||
chr16:767843 | G | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0080 others(31): Show |
39 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1596+373G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | |||||||
chr16:767843 | G | GGTC | 12 | a0002c0002t0002g0027 a0002c0002t0002g0229 a0002c0002t0002g0284 others(9): Show |
12 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+374_1596+375i others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767843 | ||||||
chr16:767843 | G | T | 40 | a0001c0001t0001g0324 a0001c0021t0001g0264 a0002c0002t0002g0001 others(37): Show |
49 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1596+373G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767843 | |||||||
chr16:767844 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596+374G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767844 | |||||||
chr16:767845 | C | G | 4 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0002c0033t0003g0253 others(1): Show |
4 | HG02647.hp1 HG03486.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+375C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767845 | |||||||
chr16:767845 | C | T | 36 | a0001c0001t0001g0070 a0001c0001t0001g0090 a0001c0001t0001g0093 others(33): Show |
41 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1596+375C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767845 | |||||||
chr16:767846 | G | C | 7 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0002c0015t0003g0071 others(4): Show |
11 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.1596+376G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767846 | |||||||
chr16:767846 | GT | G | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+377delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767846 | |||||||
chr16:767847 | T | C | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0333 others(5): Show |
8 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+377T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767847 | |||||||
chr16:767847 | T | G | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+377T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767847 | |||||||
chr16:767847 | TGGAG | T | 5 | a0001c0001t0001g0114 a0006c0011t0001g0022 a0006c0011t0001g0230 others(2): Show |
6 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+380_1596+383d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767847 | ||||||
chr16:767848 | G | C | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+378G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767848 | |||||||
chr16:767848 | GGA | G | 31 | a0001c0001t0001g0095 a0001c0001t0001g0333 a0001c0001t0001g0334 others(28): Show |
40 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1596+380_1596+381d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767848 | ||||||
chr16:767849 | G | C | 6 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0003t0002g0241 others(3): Show |
6 | HG02647.hp1 HG02723.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+379G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | |||||||
chr16:767849 | G | GGGGTGTG others(141): Show |
1 | a0001c0001t0001g0112 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1596+379_1596+380i others(150): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | |||||||
chr16:767849 | G | T | 18 | a0001c0001t0001g0092 a0001c0001t0001g0104 a0001c0001t0001g0146 others(15): Show |
19 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596+379G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | |||||||
chr16:767849 | GA | G | 6 | a0001c0021t0001g0264 a0002c0002t0002g0188 a0002c0002t0002g0301 others(3): Show |
6 | HG01192.hp1 HG01361.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+380delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767849 | |||||||
chr16:767850 | A | AG | 10 | a0001c0001t0001g0094 a0001c0001t0001g0174 a0001c0001t0001g0246 others(7): Show |
10 | HG00738.hp1 HG01106.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+386dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | AGGAGGAG others(72): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | AGGAGGGG others(97): Show |
1 | a0011c0013t0007g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(106): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | AGGAGGGG others(98): Show |
1 | a0011c0013t0006g0019 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1596+382_1596+383i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | AGGAGGGG others(98): Show |
1 | a0011c0013t0007g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1596+382_1596+383i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | AGGGGGGC others(44): Show |
4 | a0003c0004t0003g0002 a0003c0004t0003g0268 a0003c0004t0003g0269 others(1): Show |
7 | HG01106.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+386_1596+387i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767850 | A | G | 25 | a0001c0001t0001g0092 a0001c0001t0001g0104 a0001c0001t0001g0113 others(22): Show |
26 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+380A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767850 | |||||||
chr16:767850 | A | T | 6 | a0002c0002t0002g0294 a0002c0015t0003g0071 a0002c0015t0003g0172 others(3): Show |
10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+380A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767850 | |||||||
chr16:767850 | AG | A | 5 | a0006c0008t0001g0248 a0007c0007t0001g0007 a0007c0007t0001g0239 others(2): Show |
9 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+386delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767850 | ||||||
chr16:767851 | G | GGAGGGGC others(186): Show |
2 | a0004c0006t0001g0179 a0004c0006t0001g0260 |
2 | HG02080.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596+382_1596+383i others(195): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGCGCGT others(3): Show |
1 | a0002c0002t0002g0303 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1596+383_1596+384i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGGCGCG others(4): Show |
1 | a0002c0002t0002g0313 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1596+384_1596+385i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGGGCCG others(3): Show |
2 | a0001c0001t0001g0080 a0005c0005t0001g0034 |
2 | HG03492.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1596+385_1596+386i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGGGGAG others(3): Show |
1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+386_1596+387i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGGGGCG others(45): Show |
1 | a0001c0001t0001g0093 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1596+386_1596+387i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGGGGGCG others(72): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+386_1596+387i others(81): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | GGTGTGTG others(121): Show |
1 | a0001c0001t0001g0113 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767851 | ||||||
chr16:767851 | G | T | 10 | a0001c0001t0001g0095 a0001c0001t0001g0112 a0001c0001t0001g0235 others(7): Show |
10 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+381G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767851 | |||||||
chr16:767852 | G | GA | 22 | a0001c0001t0001g0324 a0002c0002t0002g0027 a0002c0002t0002g0229 others(19): Show |
23 | HG00099.hp2 HG02004.hp2 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+382_1596+383i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | |||||||
chr16:767852 | G | GAGGAGGG others(45): Show |
1 | a0002c0003t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | |||||||
chr16:767852 | G | GAGGGGCG others(166): Show |
1 | a0005c0005t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596+382_1596+383i others(175): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767852 | |||||||
chr16:767852 | G | GGGGGCGC others(92): Show |
1 | a0001c0001t0001g0124 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1596+386_1596+387i others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767852 | ||||||
chr16:767852 | GGGGGTGC others(8): Show |
G | 1 | a0005c0005t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1596+387_1596+401d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767852 | ||||||
chr16:767853 | G | GAGGCGCG others(197): Show |
1 | a0006c0008t0001g0023 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1596+383_1596+384i others(206): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | |||||||
chr16:767853 | G | GAGGCGCG others(198): Show |
1 | a0006c0008t0001g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1596+383_1596+384i others(207): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | |||||||
chr16:767853 | G | T | 1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1596+383G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767853 | |||||||
chr16:767856 | G | C | 1 | a0003c0004t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+386G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | |||||||
chr16:767856 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1596+386G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | |||||||
chr16:767856 | GT | G | 4 | a0002c0015t0003g0172 a0003c0004t0003g0003 a0003c0004t0003g0270 others(1): Show |
8 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+387delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767856 | |||||||
chr16:767857 | T | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0326 |
2 | HG00597.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1596+387T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | |||||||
chr16:767857 | T | C | 119 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0076 others(116): Show |
138 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.1596+387T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | |||||||
chr16:767857 | T | G | 24 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0112 others(21): Show |
24 | HG00621.hp1 HG00621.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+387T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767857 | |||||||
chr16:767857 | T | TGCGTGGA others(8): Show |
1 | a0001c0001t0001g0178 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1596+400_1596+414d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | ||||||
chr16:767857 | T | TGCGTGGA others(61): Show |
1 | a0002c0003t0004g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | ||||||
chr16:767857 | TGCGTGGA others(8): Show |
T | 2 | a0001c0001t0001g0277 a0020c0038t0001g0276 |
2 | HG01099.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1596+400_1596+414d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767857 | ||||||
chr16:767858 | G | A | 3 | a0001c0021t0001g0264 a0007c0007t0005g0020 a0007c0007t0005g0225 |
4 | HG01361.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+388G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767858 | |||||||
chr16:767859 | C | A | 1 | a0006c0008t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1596+389C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767859 | |||||||
chr16:767859 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0114 |
2 | NA18939.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596+389C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767859 | |||||||
chr16:767861 | TG | T | 4 | a0002c0002t0002g0303 a0002c0002t0002g0318 a0002c0002t0002g0328 others(1): Show |
4 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+393delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767861 | ||||||
chr16:767863 | G | T | 2 | a0002c0002t0002g0194 a0002c0002t0002g0313 |
2 | HG01256.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1596+393G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767863 | |||||||
chr16:767863 | GAGGAGGG others(51): Show |
G | 4 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(1): Show |
5 | HG02258.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+394_1596+451d others(60): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767863 | |||||||
chr16:767864 | A | AGGGGGCA others(3): Show |
1 | a0002c0002t0002g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | ||||||
chr16:767864 | A | AGGGGGCA others(79): Show |
1 | a0002c0002t0002g0310 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(88): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | ||||||
chr16:767864 | A | AGGGGGCA others(106): Show |
1 | a0002c0002t0002g0010 | 3 | HG02922.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1596+396_1596+397i others(115): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | ||||||
chr16:767864 | A | AGGGGGCA others(202): Show |
1 | a0002c0003t0002g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1596+396_1596+397i others(211): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | ||||||
chr16:767864 | A | AGGGGGGG others(5): Show |
32 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0026 others(29): Show |
41 | HG01069.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1596+396_1596+397i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767864 | ||||||
chr16:767864 | A | G | 3 | a0001c0001t0001g0107 a0002c0002t0002g0194 a0002c0002t0002g0313 |
3 | HG01256.hp1 HG01257.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1596+394A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767864 | |||||||
chr16:767864 | A | T | 4 | a0002c0002t0002g0303 a0002c0002t0002g0318 a0002c0002t0002g0328 others(1): Show |
4 | HG00621.hp1 HG00621.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+394A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767864 | |||||||
chr16:767865 | G | GGGCGTGG others(40): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596+396_1596+397i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | ||||||
chr16:767865 | G | GGGGGCAC others(178): Show |
1 | a0001c0001t0001g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1596+396_1596+397i others(187): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | ||||||
chr16:767865 | G | GGGGGCAC others(299): Show |
1 | a0001c0001t0001g0161 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1596+396_1596+397i others(308): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | ||||||
chr16:767865 | GGA | G | 17 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0008g0144 others(14): Show |
17 | HG00099.hp2 HG01192.hp2 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+397_1596+398d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767865 | ||||||
chr16:767866 | GA | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0112 others(7): Show |
10 | HG00738.hp2 HG02486.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+397delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767866 | |||||||
chr16:767867 | A | AGGGGCGC others(114): Show |
1 | a0018c0046t0001g0143 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1597-451_1597-331d others(123): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | AGGGGCGC others(236): Show |
1 | a0005c0005t0001g0042 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1597-453_1597-452i others(245): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | AGGGGCGC others(31): Show |
1 | a0001c0001t0001g0170 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(40): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | AGGGGCGC others(84): Show |
1 | a0005c0005t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(93): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | AGGGGCGC others(191): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1596+411_1596+412i others(200): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | AGGGGGCG others(24): Show |
1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+401_1596+402i others(33): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767867 | ||||||
chr16:767867 | A | G | 57 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0001c0001t0001g0114 others(54): Show |
69 | HG00621.hp1 HG00621.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.1596+397A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767867 | |||||||
chr16:767872 | C | G | 1 | a0003c0004t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+402C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767872 | |||||||
chr16:767873 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0237 a0001c0001t0001g0238 others(2): Show |
5 | HG02165.hp2 HG02717.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+403G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767873 | |||||||
chr16:767874 | C | A | 8 | a0001c0001t0001g0104 a0001c0001t0001g0246 a0002c0003t0004g0209 others(5): Show |
9 | HG00738.hp1 HG01943.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596+404C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767874 | |||||||
chr16:767874 | C | T | 7 | a0001c0021t0001g0264 a0002c0003t0002g0242 a0002c0015t0003g0249 others(4): Show |
7 | HG01361.hp1 HG01981.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596+404C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767874 | |||||||
chr16:767876 | T | C | 7 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(4): Show |
12 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+406T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767876 | |||||||
chr16:767876 | TGGA | T | 14 | a0001c0001t0001g0146 a0001c0001t0001g0219 a0002c0033t0003g0253 others(11): Show |
18 | HG00423.hp2 HG00558.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+415_1596+417d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767876 | ||||||
chr16:767877 | GGA | G | 3 | a0001c0001t0001g0104 a0007c0007t0005g0020 a0007c0007t0005g0225 |
4 | HG02717.hp2 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+409_1596+410d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767877 | ||||||
chr16:767879 | A | AGGAGGGG others(139): Show |
1 | a0004c0020t0001g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(148): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | ||||||
chr16:767879 | A | AGGAGGGG others(5): Show |
1 | a0011c0013t0007g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | ||||||
chr16:767879 | A | T | 3 | a0001c0021t0001g0264 a0002c0015t0003g0249 a0002c0015t0003g0250 |
3 | HG01361.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596+409A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767879 | |||||||
chr16:767879 | AGGAGGAG others(143): Show |
A | 1 | a0007c0007t0001g0052 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1596+412_1597-348d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767879 | ||||||
chr16:767880 | G | GGGGGGGG others(276): Show |
1 | a0002c0003t0004g0226 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(285): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | ||||||
chr16:767880 | G | GGGGGGGG others(275): Show |
1 | a0002c0003t0004g0228 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(284): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | ||||||
chr16:767880 | G | GGGGGGGG others(390): Show |
1 | a0002c0003t0004g0021 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(399): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | ||||||
chr16:767880 | G | GGGGGGGG others(393): Show |
1 | a0002c0003t0004g0021 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(402): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767880 | ||||||
chr16:767881 | G | GGGGGAGC others(40): Show |
1 | a0001c0001t0001g0109 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1596+411_1596+412i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | |||||||
chr16:767881 | G | GGGGGGGC others(18): Show |
4 | a0002c0003t0004g0210 a0002c0003t0004g0211 a0002c0003t0004g0213 others(1): Show |
4 | HG01978.hp1 HG02004.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+411_1596+412i others(27): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | |||||||
chr16:767881 | G | GGGGGGGG others(19): Show |
1 | a0002c0003t0002g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596+411_1596+412i others(28): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | |||||||
chr16:767881 | GAGGA | G | 20 | a0001c0001t0001g0076 a0001c0001t0001g0114 a0001c0001t0001g0237 others(17): Show |
24 | HG00639.hp1 HG01891.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596+412_1596+415d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767881 | |||||||
chr16:767882 | A | AGGGGCGC others(17): Show |
1 | a0001c0001t0011g0200 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1596+414_1596+415i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | ||||||
chr16:767882 | A | AGGGGCGC others(40): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1596+414_1596+415i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | ||||||
chr16:767882 | A | G | 12 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0246 others(9): Show |
12 | HG00597.hp2 HG00738.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+412A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767882 | |||||||
chr16:767882 | A | T | 5 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0227 others(2): Show |
6 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596+412A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767882 | |||||||
chr16:767882 | AGGAGGGG others(20): Show |
A | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1596+415_1596+441d others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767882 | ||||||
chr16:767883 | G | GGGGCGCG others(4): Show |
4 | a0004c0006t0001g0234 a0011c0013t0006g0019 a0011c0013t0007g0205 others(1): Show |
5 | HG01243.hp2 HG02257.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+414_1596+415i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767883 | ||||||
chr16:767883 | G | GGGGCGCG others(107): Show |
1 | a0002c0002t0002g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1596+414_1596+415i others(116): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767883 | ||||||
chr16:767885 | A | C | 1 | a0002c0002t0002g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1596+415A>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | |||||||
chr16:767885 | A | G | 28 | a0001c0001t0001g0109 a0001c0001t0001g0124 a0001c0001t0001g0246 others(25): Show |
30 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1596+415A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | |||||||
chr16:767885 | A | T | 2 | a0001c0001t0001g0326 a0002c0002t0002g0311 |
2 | HG00597.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+415A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767885 | |||||||
chr16:767886 | G | C | 1 | a0002c0002t0002g0311 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1596+416G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767886 | |||||||
chr16:767887 | G | T | 1 | a0002c0002t0002g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1596+417G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767887 | |||||||
chr16:767888 | G | C | 2 | a0002c0002t0002g0311 a0003c0004t0003g0267 |
2 | HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+418G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767888 | |||||||
chr16:767889 | G | C | 10 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0039t0001g0147 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+419G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767889 | |||||||
chr16:767889 | G | GGC | 5 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0003c0004t0003g0222 others(2): Show |
5 | HG02630.hp2 NA18952.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+419_1596+420i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767889 | |||||||
chr16:767890 | C | A | 7 | a0002c0002t0002g0191 a0004c0006t0001g0234 a0011c0013t0006g0019 others(4): Show |
8 | HG01243.hp2 HG02165.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+420C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | |||||||
chr16:767890 | C | G | 1 | a0001c0001t0001g0326 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596+420C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | |||||||
chr16:767890 | C | T | 1 | a0002c0002t0002g0311 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1596+420C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767890 | |||||||
chr16:767892 | C | A | 3 | a0008c0010t0002g0251 a0014c0023t0002g0037 a0014c0023t0013g0279 |
3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+422C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | |||||||
chr16:767892 | C | G | 3 | a0002c0002t0002g0191 a0002c0002t0002g0311 a0003c0004t0003g0267 |
3 | HG02165.hp2 HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+422C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | |||||||
chr16:767892 | C | T | 10 | a0001c0001t0001g0114 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG02280.hp1 HG02647.hp1 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1596+422C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | |||||||
chr16:767892 | CATGGGGG others(3): Show |
C | 1 | a0001c0001t0001g0219 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596+423_1596+432d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767892 | |||||||
chr16:767893 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0104 a0001c0001t0001g0114 others(50): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+423A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767893 | |||||||
chr16:767894 | T | G | 2 | a0002c0002t0002g0311 a0003c0004t0003g0267 |
2 | HG02258.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1596+424T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767894 | |||||||
chr16:767894 | T | TG | 12 | a0001c0001t0001g0150 a0001c0001t0001g0162 a0001c0001t0001g0169 others(9): Show |
12 | HG01169.hp1 HG01496.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+431dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767894 | ||||||
chr16:767896 | G | GA | 2 | a0003c0004t0003g0002 a0003c0004t0003g0263 |
3 | HG00423.hp2 HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1596+426_1596+427i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767896 | |||||||
chr16:767897 | G | A | 12 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0002 others(9): Show |
18 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596+427G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767897 | |||||||
chr16:767900 | G | C | 10 | a0001c0001t0001g0146 a0001c0001t0001g0326 a0001c0021t0001g0264 others(7): Show |
10 | HG00558.hp2 HG00597.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+430G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767900 | |||||||
chr16:767900 | G | T | 3 | a0006c0011t0001g0233 a0007c0007t0005g0020 a0007c0007t0005g0225 |
4 | HG01981.hp1 HG02717.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+430G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767900 | |||||||
chr16:767902 | T | A | 1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+432T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | |||||||
chr16:767902 | T | C | 44 | a0001c0001t0001g0076 a0001c0001t0001g0104 a0001c0001t0001g0146 others(41): Show |
50 | HG00558.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1596+432T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | |||||||
chr16:767902 | T | G | 8 | a0003c0004t0003g0002 a0003c0004t0003g0028 a0003c0004t0003g0263 others(5): Show |
12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+432T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767902 | |||||||
chr16:767902 | T | TGTGGAGG others(7): Show |
1 | a0005c0043t0001g0049 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1596+443_1597-453d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767902 | ||||||
chr16:767904 | T | A | 8 | a0003c0004t0003g0002 a0003c0004t0003g0028 a0003c0004t0003g0263 others(5): Show |
12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+434T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767904 | |||||||
chr16:767904 | T | C | 3 | a0008c0010t0002g0251 a0014c0023t0002g0037 a0014c0023t0013g0279 |
3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+434T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767904 | |||||||
chr16:767906 | G | C | 8 | a0003c0004t0003g0002 a0003c0004t0003g0028 a0003c0004t0003g0263 others(5): Show |
11 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+436G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767906 | |||||||
chr16:767906 | G | T | 4 | a0001c0001t0001g0104 a0008c0010t0002g0251 a0014c0023t0002g0037 others(1): Show |
4 | HG02622.hp2 HG03209.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+436G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767906 | |||||||
chr16:767907 | A | AG | 22 | a0001c0001t0001g0015 a0001c0001t0001g0065 a0001c0001t0001g0070 others(19): Show |
26 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1596+443dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | ||||||
chr16:767907 | A | AGGGGGGC others(366): Show |
1 | a0021c0025t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1596+453_1596+454i others(375): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | ||||||
chr16:767907 | A | AGGGGGGC others(104): Show |
1 | a0001c0001t0001g0004 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1597-453_1597-452i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | ||||||
chr16:767907 | A | G | 12 | a0001c0001t0001g0104 a0003c0004t0003g0002 a0003c0004t0003g0028 others(9): Show |
15 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596+437A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767907 | |||||||
chr16:767907 | A | T | 1 | a0003c0004t0003g0002 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1596+437A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767907 | |||||||
chr16:767907 | AG | A | 6 | a0001c0001t0001g0066 a0001c0001t0001g0169 a0002c0003t0004g0213 others(3): Show |
7 | HG01243.hp2 HG02257.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+443delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767907 | ||||||
chr16:767908 | G | T | 8 | a0003c0004t0003g0002 a0003c0004t0003g0028 a0003c0004t0003g0263 others(5): Show |
11 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596+438G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767908 | |||||||
chr16:767908 | GGGGGGCG others(6): Show |
G | 2 | a0002c0002t0002g0320 a0005c0005t0001g0048 |
2 | HG01978.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1596+445_1597-452d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767908 | ||||||
chr16:767909 | G | GA | 17 | a0001c0001t0001g0076 a0001c0001t0001g0114 a0001c0001t0001g0146 others(14): Show |
17 | HG00558.hp2 HG01952.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596+439_1596+440i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767909 | |||||||
chr16:767912 | G | C | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+442G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767912 | |||||||
chr16:767913 | G | C | 1 | a0003c0004t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1596+443G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767913 | |||||||
chr16:767914 | C | A | 3 | a0001c0021t0001g0264 a0002c0015t0003g0249 a0002c0015t0003g0250 |
3 | HG01361.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596+444C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | |||||||
chr16:767914 | C | CGCGTGGG others(3): Show |
3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0015c0022t0001g0030 |
3 | HG02717.hp1 HG03195.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1596+450_1596+451i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767914 | ||||||
chr16:767914 | C | G | 8 | a0003c0004t0003g0002 a0003c0004t0003g0028 a0003c0004t0003g0263 others(5): Show |
12 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596+444C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | |||||||
chr16:767914 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0134 a0001c0001t0001g0246 others(2): Show |
5 | HG00738.hp1 HG01981.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+444C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767914 | |||||||
chr16:767916 | C | A | 1 | a0016c0028t0001g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596+446C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767916 | |||||||
chr16:767916 | C | CGTGGAGG others(150): Show |
1 | a0002c0002t0002g0317 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1597-453_1597-452i others(159): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767916 | ||||||
chr16:767916 | C | T | 4 | a0002c0003t0002g0262 a0007c0007t0005g0020 a0007c0007t0005g0225 others(1): Show |
5 | HG02717.hp2 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596+446C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767916 | |||||||
chr16:767916 | CGTGGAGG others(100): Show |
C | 1 | a0001c0001t0001g0272 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1597-452_1597-346d others(2): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767916 | ||||||
chr16:767917 | G | A | 3 | a0008c0010t0002g0251 a0014c0023t0002g0037 a0014c0023t0013g0279 |
3 | HG02622.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1596+447G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767917 | |||||||
chr16:767917 | GT | G | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1596+448delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767917 | |||||||
chr16:767918 | T | C | 4 | a0003c0004t0003g0222 a0003c0004t0003g0223 a0003c0004t0003g0266 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+448T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767918 | |||||||
chr16:767921 | A | AG | 7 | a0003c0004t0003g0222 a0003c0004t0003g0223 a0003c0004t0003g0266 others(4): Show |
7 | HG02486.hp2 HG02818.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-453dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767921 | ||||||
chr16:767921 | A | AGG | 13 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(10): Show |
17 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.1597-454_1597-453d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767921 | ||||||
chr16:767921 | A | G | 17 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0021t0001g0264 others(14): Show |
19 | HG01361.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1596+451A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767921 | |||||||
chr16:767922 | G | GGA | 24 | a0001c0001t0001g0080 a0001c0001t0001g0104 a0001c0001t0001g0107 others(21): Show |
28 | HG00423.hp2 HG00597.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1596+453_1596+454i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767922 | ||||||
chr16:767924 | G | A | 1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1596+454G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767924 | |||||||
chr16:767925 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1597-454G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767925 | |||||||
chr16:767925 | GGCA | G | 8 | a0001c0021t0001g0264 a0002c0002t0002g0191 a0002c0002t0002g0311 others(5): Show |
8 | HG01361.hp1 HG02109.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1597-453_1597-451d others(5): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767925 | |||||||
chr16:767926 | GCACGTGG others(6): Show |
G | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1597-451_1597-439d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767926 | ||||||
chr16:767927 | C | CGCATGGG others(3): Show |
1 | a0008c0010t0002g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1597-452_1597-451i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | |||||||
chr16:767927 | C | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0146 others(3): Show |
7 | HG00558.hp2 HG01952.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-452C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | |||||||
chr16:767927 | CA | C | 4 | a0002c0003t0002g0242 a0011c0013t0006g0019 a0011c0013t0007g0205 others(1): Show |
5 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-451delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767927 | |||||||
chr16:767928 | A | ACGTGGAG others(112): Show |
1 | a0004c0016t0001g0139 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1597-443_1597-442i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767928 | ||||||
chr16:767928 | A | AG | 5 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0146 others(2): Show |
5 | HG00558.hp2 HG01952.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-451_1597-450i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | |||||||
chr16:767928 | A | AGCGTGGG others(295): Show |
1 | a0005c0005t0001g0012 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1597-451_1597-450i others(304): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | |||||||
chr16:767928 | A | G | 65 | a0001c0001t0001g0080 a0001c0001t0001g0104 a0001c0001t0001g0107 others(62): Show |
76 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1597-451A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767928 | |||||||
chr16:767929 | C | A | 9 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(6): Show |
13 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-450C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767929 | |||||||
chr16:767929 | C | T | 2 | a0002c0002t0002g0191 a0002c0002t0002g0311 |
2 | HG02165.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-450C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767929 | |||||||
chr16:767930 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1597-449G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767930 | |||||||
chr16:767932 | G | GGGGGGGC others(100): Show |
2 | a0008c0010t0002g0013 a0008c0010t0002g0053 |
3 | HG01891.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1597-446_1597-445i others(109): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767932 | ||||||
chr16:767932 | G | GGGGGGGC others(101): Show |
1 | a0008c0010t0002g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1597-446_1597-445i others(110): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767932 | ||||||
chr16:767933 | GA | G | 3 | a0011c0013t0006g0019 a0011c0013t0007g0205 a0011c0013t0007g0206 |
4 | HG01243.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-445delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767933 | |||||||
chr16:767934 | A | AG | 28 | a0001c0001t0001g0066 a0001c0001t0001g0219 a0001c0001t0001g0333 others(25): Show |
38 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1597-441dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGG | 9 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0002c0015t0003g0071 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-442_1597-441d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGAGGAG others(88): Show |
1 | a0025c0035t0001g0181 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1597-443_1597-442i others(97): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGAGGGG others(113): Show |
1 | a0001c0001t0001g0104 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1597-443_1597-442i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGAGGGG others(230): Show |
1 | a0001c0001t0001g0113 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1597-443_1597-442i others(239): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGGGGGA others(4): Show |
2 | a0002c0003t0004g0213 a0002c0033t0003g0253 |
2 | HG02273.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGGGGGA others(87): Show |
1 | a0001c0001t0001g0080 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGGGGGG others(168): Show |
1 | a0002c0003t0004g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(177): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | AGGGGGGG others(290): Show |
1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1597-441_1597-440i others(299): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767934 | A | G | 12 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0114 others(9): Show |
13 | HG00558.hp2 HG01257.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1597-445A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767934 | |||||||
chr16:767934 | A | T | 1 | a0002c0003t0002g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1597-445A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767934 | |||||||
chr16:767934 | AGGGGTCG others(3): Show |
A | 5 | a0006c0008t0001g0011 a0006c0008t0001g0032 a0006c0008t0001g0035 others(2): Show |
5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-442_1597-433d others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767934 | ||||||
chr16:767935 | G | GGA | 5 | a0001c0001t0001g0246 a0001c0021t0001g0264 a0002c0015t0003g0249 others(2): Show |
5 | HG00738.hp1 HG01361.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-443_1597-442i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGCCG others(62): Show |
1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(71): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGGAG others(3): Show |
3 | a0001c0001t0001g0112 a0001c0039t0001g0147 a0004c0016t0001g0257 |
3 | HG03834.hp1 NA18939.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGGCG others(121): Show |
2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG02723.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGGGA others(4): Show |
1 | a0001c0001t0001g0326 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGGGC others(45): Show |
1 | a0015c0022t0001g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1597-441_1597-440i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767935 | G | GGGGGGGT others(60): Show |
2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1597-441_1597-440i others(69): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767935 | ||||||
chr16:767936 | GGGTC | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0114 a0001c0001t0001g0146 others(1): Show |
4 | HG00558.hp2 HG03669.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-441_1597-438d others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767936 | ||||||
chr16:767939 | T | A | 1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-440T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | |||||||
chr16:767939 | T | C | 5 | a0003c0004t0003g0222 a0003c0004t0003g0223 a0003c0004t0003g0265 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-440T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | |||||||
chr16:767939 | T | G | 80 | a0001c0001t0001g0080 a0001c0001t0001g0095 a0001c0001t0001g0104 others(77): Show |
94 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1597-440T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | |||||||
chr16:767939 | T | TCGCGTGG others(496): Show |
1 | a0001c0001t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(505): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767939 | ||||||
chr16:767939 | T | TCGCGTGG others(214): Show |
1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(223): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767939 | ||||||
chr16:767939 | T | TGTGGAGG others(4): Show |
2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18952.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1597-440_1597-439i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767939 | |||||||
chr16:767940 | C | CCGCGTGG others(4): Show |
1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-439_1597-438i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | |||||||
chr16:767940 | C | CGCGTGGA others(121): Show |
1 | a0002c0002t0002g0278 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(130): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | ||||||
chr16:767940 | C | CGCGTGGA others(17): Show |
2 | a0002c0003t0002g0254 a0002c0003t0004g0211 |
2 | HG01934.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | ||||||
chr16:767940 | C | CGCGTGGA others(180): Show |
1 | a0002c0003t0004g0214 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(189): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767940 | ||||||
chr16:767940 | C | G | 22 | a0001c0001t0001g0112 a0001c0001t0001g0235 a0001c0001t0001g0236 others(19): Show |
24 | HG00597.hp2 HG01243.hp2 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597-439C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | |||||||
chr16:767940 | C | T | 6 | a0001c0001t0001g0080 a0002c0003t0004g0215 a0005c0005t0001g0012 others(3): Show |
7 | HG02622.hp2 HG03209.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-439C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767940 | |||||||
chr16:767941 | G | A | 1 | a0002c0002t0002g0191 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1597-438G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767941 | |||||||
chr16:767941 | G | GCGTGGAG others(191): Show |
1 | a0004c0006t0001g0255 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(200): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767941 | ||||||
chr16:767942 | C | A | 4 | a0002c0003t0002g0241 a0002c0003t0002g0243 a0003c0004t0003g0267 others(1): Show |
4 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-437C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767942 | |||||||
chr16:767942 | C | CGTGGAGG others(69): Show |
1 | a0004c0006t0001g0179 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1597-418_1597-417i others(78): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767942 | ||||||
chr16:767942 | C | CGTGGAGG others(115): Show |
1 | a0002c0003t0004g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767942 | ||||||
chr16:767942 | C | G | 1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-437C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767942 | |||||||
chr16:767943 | G | A | 2 | a0002c0002t0002g0191 a0002c0002t0002g0311 |
2 | HG02165.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-436G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767943 | |||||||
chr16:767944 | T | C | 1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-435T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767944 | |||||||
chr16:767944 | TG | T | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-433delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767944 | ||||||
chr16:767945 | GGA | G | 6 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(3): Show |
10 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-432_1597-431d others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767945 | ||||||
chr16:767946 | G | C | 1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-433G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767946 | |||||||
chr16:767947 | A | AGGGGGGA others(99): Show |
1 | a0002c0003t0004g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767947 | ||||||
chr16:767947 | A | T | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-432A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767947 | |||||||
chr16:767948 | G | GGGGGGAG others(59): Show |
3 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0228 |
4 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-430_1597-429i others(68): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGAG others(113): Show |
1 | a0002c0003t0004g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGCG others(111): Show |
1 | a0004c0006t0001g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGCG others(94): Show |
1 | a0004c0006t0001g0260 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1597-430_1597-429i others(103): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGCG others(109): Show |
7 | a0004c0006t0001g0220 a0004c0006t0001g0245 a0004c0006t0001g0259 others(4): Show |
7 | HG00558.hp1 HG03927.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-430_1597-429i others(118): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGCG others(123): Show |
2 | a0027c0032t0001g0327 a0030c0031t0001g0176 |
2 | NA18950.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(132): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGCG others(110): Show |
2 | a0004c0006t0001g0261 a0004c0016t0001g0258 |
2 | HG00642.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1597-430_1597-429i others(119): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | GGGGGGGC others(111): Show |
1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(120): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767948 | ||||||
chr16:767948 | G | T | 1 | a0005c0005t0001g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1597-431G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767948 | |||||||
chr16:767949 | G | GGGGGAGC others(87): Show |
1 | a0002c0003t0004g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1597-430_1597-429i others(96): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767949 | |||||||
chr16:767949 | GA | G | 19 | a0001c0021t0001g0175 a0002c0003t0002g0241 a0002c0003t0002g0243 others(16): Show |
23 | HG00423.hp2 HG01106.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1597-429delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767949 | |||||||
chr16:767950 | A | AGGGGCGC others(281): Show |
1 | a0001c0001t0001g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(290): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767950 | ||||||
chr16:767950 | A | AGGGGCGC others(41): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0057 |
2 | HG00280.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1597-412_1597-411i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767950 | ||||||
chr16:767950 | A | G | 42 | a0001c0001t0001g0107 a0001c0001t0001g0219 a0001c0001t0001g0246 others(39): Show |
48 | HG00558.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1597-429A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767950 | |||||||
chr16:767955 | C | A | 1 | a0002c0003t0004g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1597-424C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | |||||||
chr16:767955 | C | G | 2 | a0001c0001t0001g0197 a0005c0005t0001g0034 |
2 | NA18949.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1597-424C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | |||||||
chr16:767955 | C | T | 1 | a0002c0002t0002g0311 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1597-424C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767955 | |||||||
chr16:767955 | CGCGTGGA others(17): Show |
C | 1 | a0002c0003t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1597-411_1597-388d others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767955 | ||||||
chr16:767956 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1597-423G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767956 | |||||||
chr16:767957 | C | A | 2 | a0001c0001t0001g0246 a0016c0028t0001g0221 |
2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1597-422C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767957 | |||||||
chr16:767957 | C | CGTGGGGG others(3): Show |
3 | a0001c0021t0001g0175 a0007c0007t0001g0007 a0007c0007t0001g0239 |
5 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-418_1597-417i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767957 | ||||||
chr16:767958 | G | A | 14 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(11): Show |
18 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1597-421G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767958 | |||||||
chr16:767959 | T | C | 1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-420T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767959 | |||||||
chr16:767961 | G | GGGGGGCG others(83): Show |
1 | a0002c0003t0004g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1597-418_1597-417i others(92): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | |||||||
chr16:767961 | G | GGGGGGTG others(40): Show |
2 | a0007c0007t0001g0240 a0013c0018t0001g0009 |
4 | HG02451.hp1 HG02572.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-418_1597-417i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | |||||||
chr16:767961 | GA | G | 4 | a0001c0001t0001g0107 a0002c0003t0002g0241 a0002c0003t0002g0243 others(1): Show |
4 | HG01257.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-417delA | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767961 | |||||||
chr16:767962 | A | AG | 13 | a0001c0001t0001g0162 a0001c0001t0001g0174 a0001c0001t0001g0336 others(10): Show |
14 | HG01169.hp1 HG01175.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597-412dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | ||||||
chr16:767962 | A | AGGGGGGC others(15): Show |
1 | a0002c0002t0002g0322 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(24): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | ||||||
chr16:767962 | A | AGGGGGGG others(40): Show |
1 | a0002c0002t0002g0329 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1597-412_1597-411i others(49): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | ||||||
chr16:767962 | A | AGGGGGGG others(49): Show |
1 | a0011c0013t0007g0205 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1597-412_1597-411i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767962 | ||||||
chr16:767962 | A | G | 15 | a0002c0002t0002g0311 a0002c0003t0004g0209 a0002c0003t0004g0227 others(12): Show |
21 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1597-417A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767962 | |||||||
chr16:767964 | G | GAGGA | 9 | a0001c0001t0001g0080 a0002c0003t0004g0207 a0008c0010t0002g0013 others(6): Show |
10 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-415_1597-414i others(6): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767964 | |||||||
chr16:767966 | G | C | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-413G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767966 | |||||||
chr16:767967 | G | T | 5 | a0006c0008t0001g0011 a0006c0008t0001g0032 a0006c0008t0001g0035 others(2): Show |
5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-412G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767967 | |||||||
chr16:767968 | C | CG | 6 | a0002c0002t0002g0311 a0002c0003t0004g0021 a0002c0003t0004g0210 others(3): Show |
7 | HG01978.hp1 HG02004.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-411_1597-410i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | |||||||
chr16:767968 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0080 others(105): Show |
128 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.1597-411C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | |||||||
chr16:767968 | C | T | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-411C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | |||||||
chr16:767968 | CCGTGTGG others(46): Show |
C | 2 | a0007c0007t0005g0020 a0007c0007t0005g0225 |
3 | HG02717.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1597-410_1597-358d others(55): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767968 | |||||||
chr16:767969 | C | A | 8 | a0001c0021t0001g0264 a0002c0003t0002g0254 a0002c0003t0004g0211 others(5): Show |
9 | HG01361.hp1 HG01934.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-410C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | |||||||
chr16:767969 | C | CGCGTGGG others(27): Show |
1 | a0002c0002t0002g0320 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1597-409_1597-408i others(36): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767969 | ||||||
chr16:767969 | C | G | 6 | a0002c0003t0004g0209 a0002c0015t0003g0071 a0002c0015t0003g0172 others(3): Show |
10 | HG00639.hp1 HG01891.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-410C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | |||||||
chr16:767969 | C | T | 5 | a0006c0008t0001g0011 a0006c0008t0001g0032 a0006c0008t0001g0035 others(2): Show |
5 | HG02451.hp2 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-410C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767969 | |||||||
chr16:767970 | G | T | 1 | a0002c0003t0004g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1597-409G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767970 | |||||||
chr16:767971 | T | A | 10 | a0002c0003t0004g0212 a0002c0015t0003g0071 a0002c0015t0003g0172 others(7): Show |
14 | HG00639.hp1 HG01891.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1597-408T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | |||||||
chr16:767971 | T | C | 99 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0080 others(96): Show |
121 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1597-408T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | |||||||
chr16:767971 | T | G | 6 | a0002c0003t0004g0209 a0006c0008t0001g0011 a0006c0008t0001g0032 others(3): Show |
6 | HG01943.hp2 HG02451.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-408T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767971 | |||||||
chr16:767972 | G | A | 21 | a0001c0001t0001g0080 a0002c0003t0002g0241 a0002c0003t0002g0243 others(18): Show |
24 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1597-407G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767972 | G | GGA | 5 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-407_1597-406i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767972 | G | GGGGGGGC others(3): Show |
3 | a0002c0003t0004g0021 a0002c0003t0004g0226 a0002c0003t0004g0228 |
4 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-407_1597-406i others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767972 | G | GGGGGGGC others(4): Show |
1 | a0002c0003t0004g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-407_1597-406i others(13): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767972 | G | GGGGGGGC others(98): Show |
1 | a0002c0003t0004g0213 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1597-407_1597-406i others(107): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767972 | G | GTGGGGGG others(6): Show |
2 | a0001c0001t0001g0246 a0001c0039t0001g0147 |
2 | HG00738.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1597-399_1597-398i others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767972 | ||||||
chr16:767972 | G | GTGGGGGG others(369): Show |
1 | a0002c0003t0004g0208 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1597-399_1597-398i others(378): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767972 | ||||||
chr16:767972 | GT | G | 5 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-406delT | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767972 | |||||||
chr16:767973 | T | A | 2 | a0002c0002t0002g0311 a0002c0003t0004g0209 |
2 | HG01943.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-406T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767973 | |||||||
chr16:767973 | T | G | 12 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(9): Show |
12 | HG01978.hp1 HG02004.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1597-406T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767973 | |||||||
chr16:767973 | T | TGGAGGGG others(62): Show |
1 | a0014c0045t0003g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-404_1597-403i others(71): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | T | TGGAGGGG others(32): Show |
1 | a0003c0004t0003g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1597-404_1597-403i others(41): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | T | TGGAGGGG others(33): Show |
3 | a0003c0004t0003g0222 a0003c0004t0003g0266 a0003c0004t0003g0280 |
3 | HG02486.hp2 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1597-404_1597-403i others(42): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | T | TGGAGGGG others(49): Show |
1 | a0011c0013t0007g0206 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1597-404_1597-403i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | T | TGGAGGGG others(50): Show |
1 | a0011c0013t0006g0019 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1597-404_1597-403i others(59): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | T | TGGGAGGG others(75): Show |
1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1597-403_1597-402i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767973 | TG | T | 8 | a0001c0001t0001g0103 a0002c0002t0002g0294 a0003c0004t0003g0267 others(5): Show |
9 | HG00733.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-399delG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767973 | ||||||
chr16:767979 | G | C | 19 | a0002c0015t0003g0071 a0002c0015t0003g0172 a0003c0004t0003g0003 others(16): Show |
24 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597-400G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | |||||||
chr16:767979 | G | GCGTGGAG others(112): Show |
1 | a0003c0004t0003g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1597-400_1597-399i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | |||||||
chr16:767979 | G | GGCGTGGA others(8): Show |
1 | a0001c0001t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | ||||||
chr16:767979 | G | GGGCGCAT others(20): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0326 a0016c0028t0001g0221 |
3 | HG00597.hp2 HG01884.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1597-399_1597-398i others(29): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | ||||||
chr16:767979 | G | GGT | 7 | a0001c0001t0001g0218 a0002c0002t0002g0278 a0002c0002t0002g0317 others(4): Show |
9 | HG00621.hp1 HG01109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-399_1597-398i others(4): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | ||||||
chr16:767979 | G | GGTGTGGA others(41): Show |
1 | a0002c0003t0002g0247 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1597-399_1597-398i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767979 | ||||||
chr16:767979 | G | T | 8 | a0001c0001t0001g0219 a0001c0001t0001g0333 a0001c0001t0001g0334 others(5): Show |
10 | HG01952.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-400G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767979 | |||||||
chr16:767980 | G | C | 1 | a0021c0025t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1597-399G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767980 | |||||||
chr16:767981 | C | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0080 others(56): Show |
73 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1597-398C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767981 | |||||||
chr16:767982 | G | A | 5 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0231 others(2): Show |
6 | HG01981.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-397G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767982 | |||||||
chr16:767985 | G | T | 1 | a0002c0002t0002g0311 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1597-394G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767985 | |||||||
chr16:767986 | A | AGGGGGGC others(42): Show |
2 | a0002c0002t0002g0027 a0002c0002t0002g0321 |
2 | HG00099.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1597-384_1597-383i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | ||||||
chr16:767986 | A | AGGGGGGC others(43): Show |
1 | a0002c0002t0012g0027 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1597-384_1597-383i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | ||||||
chr16:767986 | A | AGTGGGGT others(8): Show |
1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1597-392_1597-391i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767986 | ||||||
chr16:767986 | A | G | 2 | a0001c0021t0001g0175 a0002c0002t0002g0311 |
2 | HG03669.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1597-393A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767986 | |||||||
chr16:767987 | G | GGGGGGCG others(104): Show |
1 | a0001c0001t0001g0051 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1597-332_1597-331i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | ||||||
chr16:767987 | G | GGGGGGCG others(227): Show |
2 | a0006c0008t0001g0023 a0006c0008t0001g0252 |
3 | HG01069.hp2 HG01071.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1597-380_1597-379i others(236): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | ||||||
chr16:767987 | G | GGGGGGCG others(1265): Show |
1 | a0006c0008t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1597-380_1597-379i others(1274): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767987 | ||||||
chr16:767988 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1597-391G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GA | 48 | a0001c0001t0001g0112 a0001c0001t0001g0218 a0001c0001t0001g0219 others(45): Show |
56 | HG00597.hp2 HG00621.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(3): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(103): Show |
2 | a0003c0004t0003g0028 a0003c0004t0003g0337 |
3 | HG01884.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(112): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(117): Show |
4 | a0003c0004t0003g0002 a0003c0004t0003g0268 a0003c0004t0003g0269 others(1): Show |
7 | HG01106.hp2 HG02109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(126): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(118): Show |
2 | a0002c0015t0003g0249 a0002c0015t0003g0250 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(127): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(119): Show |
1 | a0003c0004t0003g0263 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(128): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(120): Show |
1 | a0002c0033t0003g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(129): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(246): Show |
1 | a0005c0005t0001g0031 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(255): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(91): Show |
1 | a0002c0003t0002g0242 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(115): Show |
1 | a0002c0003t0002g0254 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(124): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(116): Show |
1 | a0002c0003t0004g0211 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(125): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(75): Show |
1 | a0004c0006t0001g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(90): Show |
11 | a0004c0006t0001g0179 a0004c0006t0001g0220 a0004c0006t0001g0245 others(8): Show |
11 | HG00558.hp1 HG02071.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.1597-391_1597-390i others(99): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(90): Show |
3 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0001g0238 |
3 | HG02717.hp1 HG03195.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1597-391_1597-390i others(99): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(91): Show |
1 | a0004c0020t0001g0330 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(100): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(128): Show |
1 | a0004c0006t0001g0234 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1597-391_1597-390i others(137): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GAGGGGCG others(92): Show |
1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-391_1597-390i others(101): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767988 | |||||||
chr16:767988 | G | GGGCACGT others(99): Show |
1 | a0001c0021t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1597-389_1597-388i others(108): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCAC others(44): Show |
1 | a0002c0002t0002g0323 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1597-386_1597-385i others(53): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCAC others(43): Show |
2 | a0002c0002t0002g0299 a0002c0002t0002g0310 |
2 | HG03942.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1597-386_1597-385i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCAC others(42): Show |
33 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0025 others(30): Show |
44 | HG00733.hp2 HG01069.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1597-386_1597-385i others(51): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCAC others(43): Show |
2 | a0002c0002t0002g0283 a0002c0002t0002g0302 |
2 | HG02080.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1597-386_1597-385i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(216): Show |
1 | a0009c0030t0002g0338 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1597-384_1597-383i others(225): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(8): Show |
1 | a0003c0004t0003g0267 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1597-388_1597-374d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(154): Show |
1 | a0001c0001t0001g0275 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1597-335_1597-334i others(163): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(122): Show |
1 | a0001c0001t0001g0018 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1597-332_1597-331i others(131): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(127): Show |
1 | a0001c0001t0001g0146 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(112): Show |
1 | a0001c0001t0001g0142 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(121): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGCGC others(89): Show |
1 | a0001c0001t0001g0236 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1597-377_1597-376i others(98): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGGCA others(43): Show |
1 | a0002c0002t0002g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1597-387_1597-386i others(52): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGGCG others(61): Show |
1 | a0015c0022t0001g0030 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1597-387_1597-386i others(70): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767988 | G | GGGGGTGC others(8): Show |
9 | a0001c0039t0001g0147 a0002c0003t0004g0021 a0002c0003t0004g0208 others(6): Show |
10 | HG01978.hp1 HG02004.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-387_1597-386i others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767988 | ||||||
chr16:767993 | C | T | 1 | a0008c0010t0002g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-386C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767993 | |||||||
chr16:767994 | G | A | 1 | a0002c0002t0002g0303 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-385G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767994 | |||||||
chr16:767995 | C | A | 2 | a0002c0003t0004g0214 a0002c0003t0004g0215 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1597-384C>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767995 | |||||||
chr16:767996 | G | A | 1 | a0002c0002t0002g0303 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-383G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 767996 | |||||||
chr16:767997 | TGGAGGAG others(24): Show |
T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-379_1597-349d others(33): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 767997 | ||||||
chr16:768000 | A | AGGAGGAG others(45): Show |
1 | a0005c0005t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1597-329_1597-328i others(54): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | ||||||
chr16:768000 | A | AGGGGGGC others(41): Show |
2 | a0002c0003t0004g0214 a0002c0003t0004g0215 |
2 | HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1597-377_1597-376i others(50): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | ||||||
chr16:768000 | A | AGGGGGGG others(5): Show |
1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-377_1597-376i others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | ||||||
chr16:768000 | A | AGGGGGGG others(17): Show |
2 | a0007c0007t0001g0007 a0007c0007t0001g0239 |
4 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-377_1597-376i others(26): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768000 | ||||||
chr16:768000 | A | G | 9 | a0002c0002t0002g0303 a0002c0003t0004g0207 a0008c0010t0002g0013 others(6): Show |
10 | HG01516.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-379A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768000 | |||||||
chr16:768001 | G | GGGGGCGC | 7 | a0002c0003t0004g0207 a0008c0010t0002g0013 a0008c0010t0002g0053 others(4): Show |
8 | HG01891.hp2 HG02055.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1597-377_1597-376i others(9): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768001 | ||||||
chr16:768003 | A | AGGGGCGC others(57): Show |
1 | a0008c0010t0002g0038 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1597-374_1597-373i others(66): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768003 | ||||||
chr16:768003 | A | G | 2 | a0001c0021t0001g0264 a0014c0023t0002g0037 |
2 | HG01361.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1597-376A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768003 | |||||||
chr16:768003 | A | T | 8 | a0002c0002t0002g0303 a0002c0003t0004g0207 a0008c0010t0002g0013 others(5): Show |
9 | HG01516.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1597-376A>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768003 | |||||||
chr16:768006 | A | G | 14 | a0001c0021t0001g0264 a0002c0002t0002g0303 a0002c0003t0004g0207 others(11): Show |
15 | HG00642.hp1 HG01361.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1597-373A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768006 | |||||||
chr16:768013 | C | T | 1 | a0002c0002t0002g0303 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-366C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768013 | |||||||
chr16:768014 | A | G | 9 | a0002c0002t0002g0056 a0002c0002t0002g0303 a0004c0006t0001g0261 others(6): Show |
13 | HG00642.hp1 HG01516.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-365A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768014 | |||||||
chr16:768015 | T | G | 1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-364T>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768015 | |||||||
chr16:768015 | T | TGGGGGGG others(49): Show |
1 | a0002c0002t0002g0304 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1597-319_1597-318i others(58): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768015 | ||||||
chr16:768021 | G | C | 7 | a0004c0006t0001g0183 a0004c0006t0001g0261 a0004c0006t0001g0335 others(4): Show |
9 | HG00642.hp1 HG02055.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-358G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768021 | |||||||
chr16:768023 | T | A | 4 | a0004c0006t0001g0261 a0004c0006t0001g0335 a0004c0016t0001g0258 others(1): Show |
4 | HG00642.hp1 HG03540.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-356T>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768023 | |||||||
chr16:768023 | T | C | 7 | a0001c0021t0001g0264 a0004c0006t0001g0183 a0007c0007t0001g0007 others(4): Show |
12 | HG01361.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1597-356T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768023 | |||||||
chr16:768028 | A | AG | 14 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0164 others(11): Show |
16 | HG00639.hp2 HG01070.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1597-345dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768028 | ||||||
chr16:768029 | G | GGGGGGCG others(6): Show |
11 | a0001c0001t0001g0246 a0002c0003t0002g0241 a0002c0003t0002g0242 others(8): Show |
13 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-334_1597-322d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768029 | ||||||
chr16:768029 | GGGGGGCG others(6): Show |
G | 17 | a0001c0001t0001g0272 a0001c0021t0001g0175 a0002c0002t0002g0306 others(14): Show |
17 | HG00558.hp1 HG01074.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.1597-334_1597-322d others(15): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768029 | ||||||
chr16:768030 | G | A | 1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-349G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768030 | |||||||
chr16:768030 | GGGGGCGC others(5): Show |
G | 1 | a0004c0006t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1597-344_1597-333d others(14): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768030 | ||||||
chr16:768034 | GC | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0107 a0001c0001t0001g0235 others(3): Show |
6 | HG01257.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1597-344delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768034 | |||||||
chr16:768035 | C | T | 1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-344C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768035 | |||||||
chr16:768036 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-343G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768036 | |||||||
chr16:768036 | G | T | 1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-343G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768036 | |||||||
chr16:768037 | C | CGTGGAGG others(113): Show |
1 | a0015c0022t0001g0029 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(122): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768037 | ||||||
chr16:768037 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0001g0235 a0001c0001t0001g0236 others(2): Show |
5 | HG01257.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-342C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768037 | |||||||
chr16:768040 | G | GGGGGGGG others(76): Show |
1 | a0004c0016t0001g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1597-338_1597-337i others(85): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768040 | ||||||
chr16:768041 | G | GGGGGGGC others(75): Show |
2 | a0004c0006t0001g0261 a0004c0006t0001g0335 |
2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1597-338_1597-337i others(84): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768041 | |||||||
chr16:768041 | G | GGGGGGGT others(147): Show |
1 | a0002c0002t0002g0312 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1597-338_1597-337i others(156): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768041 | |||||||
chr16:768042 | A | AG | 9 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0001g0154 others(6): Show |
9 | HG00408.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1597-332dupG | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGAGGAG others(23): Show |
1 | a0002c0002t0002g0303 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-335_1597-334i others(32): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGAGGGG others(37): Show |
1 | a0001c0021t0001g0264 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1597-335_1597-334i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGCA others(127): Show |
1 | a0021c0025t0001g0167 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(136): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGCA others(150): Show |
3 | a0002c0002t0002g0027 a0002c0002t0002g0321 a0002c0002t0012g0027 |
3 | HG00099.hp2 HG02004.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1597-331_1597-330i others(159): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGCC others(157): Show |
1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-331_1597-330i others(166): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGCG others(7): Show |
1 | a0006c0008t0001g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1597-335_1597-322d others(16): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGGG others(22): Show |
2 | a0007c0007t0001g0007 a0007c0007t0001g0239 |
4 | HG02055.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-332_1597-331i others(31): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGGG others(37): Show |
1 | a0013c0018t0001g0009 | 3 | HG02451.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1597-332_1597-331i others(46): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | AGGGGGGG others(104): Show |
1 | a0004c0006t0001g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1597-332_1597-331i others(113): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768042 | ||||||
chr16:768042 | A | G | 5 | a0002c0002t0002g0312 a0004c0006t0001g0261 a0004c0006t0001g0335 others(2): Show |
5 | HG00642.hp1 HG03540.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-337A>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768042 | |||||||
chr16:768044 | G | A | 2 | a0002c0002t0002g0025 a0002c0002t0002g0322 |
3 | NA18943.hp1 NA18945.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1597-335G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768044 | |||||||
chr16:768048 | C | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0009c0012t0001g0008 |
4 | HG01109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-331C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768048 | |||||||
chr16:768051 | G | A | 1 | a0005c0005t0001g0048 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1597-328G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768051 | |||||||
chr16:768051 | GTGGAGGA others(8): Show |
G | 3 | a0012c0017t0001g0082 a0012c0017t0001g0083 a0012c0017t0001g0184 |
3 | HG01123.hp1 HG01256.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1597-321_1597-307d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768051 | ||||||
chr16:768073 | G | C | 4 | a0006c0011t0001g0022 a0006c0011t0001g0230 a0006c0011t0001g0232 others(1): Show |
5 | HG01981.hp1 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-306G>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768073 | |||||||
chr16:768077 | G | T | 6 | a0002c0003t0004g0021 a0002c0003t0004g0214 a0002c0003t0004g0215 others(3): Show |
7 | HG02647.hp2 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597-302G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768077 | |||||||
chr16:768090 | GC | G | 3 | a0001c0001t0001g0145 a0002c0002t0002g0294 a0021c0025t0001g0167 |
3 | HG00408.hp1 HG01175.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1597-286delC | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768090 | ||||||
chr16:768114 | G | T | 1 | a0002c0024t0002g0282 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1597-265G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768114 | |||||||
chr16:768118 | G | T | 22 | a0001c0001t0011g0200 a0002c0015t0003g0071 a0002c0015t0003g0172 others(19): Show |
30 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1597-261G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768118 | |||||||
chr16:768153 | C | G | 1 | a0004c0006t0001g0183 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1597-226C>G | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768153 | |||||||
chr16:768173 | AGGAAGGG others(28): Show |
A | 1 | a0003c0004t0003g0269 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1597-194_1597-160d others(37): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768173 | ||||||
chr16:768193 | G | A | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1597-186G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768193 | |||||||
chr16:768212 | AGGGCAGC others(8): Show |
A | 1 | a0002c0002t0002g0284 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1597-166_1597-152d others(17): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768212 | |||||||
chr16:768242 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1597-137C>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768242 | |||||||
chr16:768253 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1597-126G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768253 | |||||||
chr16:768294 | G | A | 1 | a0002c0033t0003g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1597-85G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768294 | |||||||
chr16:768325 | G | T | 2 | a0001c0021t0001g0264 a0004c0006t0001g0234 |
2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1597-54G>T | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | chr16 | 768325 | |||||||
chr16:768353 | TGATGGCT others(5): Show |
T | 1 | a0017c0019t0002g0285 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1597-24_1597-13del others(12): Show |
MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr16 | 768353 | ||||||
chr16:768582 | G | A | 1 | a0002c0003t0004g0212 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1783+17G>A | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/17 | chr16 | 768582 | |||||||
chr16:768643 | T | C | 26 | a0002c0003t0002g0262 a0002c0015t0003g0071 a0002c0015t0003g0172 others(23): Show |
35 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.1784-5T>C | MSLN | ENSG00000102854.16 | transcript | ENST00000545450.7 | protein_coding | 17/17 | chr16 | 768643 |