Item | Value |
---|---|
geneid | 3340 |
ensemblid | ENSG00000070614.15 |
hgncid | 7680 |
symbol | NDST1 |
name | N-deacetylase and N-sulfotransferase 1 |
refseq_nuc | NM_001543.5 |
refseq_prot | NP_001534.1 |
ensembl_nuc | ENST00000261797.7 |
ensembl_prot | ENSP00000261797.6 |
mane_status | MANE Select |
chr | chr5 |
start | 150508131 |
end | 150558211 |
strand | + |
ver | v1.2 |
region | chr5:150508131-150558211 |
region5000 | chr5:150503131-150563211 |
regionname0 | NDST1_chr5_150508131_150558211 |
regionname5000 | NDST1_chr5_150503131_150563211 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 882 | 393 | 97 | 64 | 175 | 12 | 43 | 135 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
a0002 | 0/0 | 882 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
a0003 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
a0004 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
a0005 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
a0006 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | MPALA others(877): Show |
chr5 | 150503131 | 150563211 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2646 | 204 | 70 | 20 | 98 | 3 | 13 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0002 | 0/0 | 2646 | 75 | 7 | 26 | 23 | 3 | 16 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0003 | 0/0 | 2646 | 28 | 0 | 0 | 27 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0004 | 1/0 | 2646 | 19 | 1 | 4 | 10 | 1 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0005 | 0/1 | 2646 | 13 | 2 | 7 | 0 | 2 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0006 | 0/0 | 2646 | 10 | 10 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0007 | 0/0 | 2646 | 9 | 0 | 0 | 9 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0008 | 0/0 | 2646 | 8 | 0 | 0 | 0 | 0 | 8 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0009 | 0/0 | 2646 | 8 | 0 | 5 | 0 | 1 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0010 | 0/0 | 2646 | 7 | 0 | 2 | 4 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0011 | 0/0 | 2646 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0013 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0014 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0015 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0016 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0017 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0018 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0019 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0021 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0022 | 0/0 | 2646 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0001c0025 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0002c0012 | 0/0 | 2646 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0003c0026 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0004c0024 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0005c0020 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 | ||
a0006c0023 | 0/0 | 2646 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | ATGCC others(2641): Show |
chr5 | 150503131 | 150563211 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8011 | 64 | 5 | 15 | 39 | 2 | 3 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0002 | 0/0 | 8013 | 30 | 7 | 2 | 19 | 0 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0004 | 0/0 | 8011 | 22 | 0 | 0 | 21 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0006 | 0/0 | 8015 | 3 | 1 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0007 | 0/0 | 8011 | 12 | 12 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0008 | 0/0 | 8013 | 12 | 8 | 0 | 0 | 0 | 4 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0011 | 0/0 | 8011 | 6 | 6 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0016 | 0/0 | 8013 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0017 | 0/0 | 8013 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0019 | 0/0 | 8015 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0021 | 0/0 | 8011 | 3 | 0 | 0 | 3 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0024 | 0/0 | 8011 | 2 | 1 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0025 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0026 | 0/0 | 8011 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0027 | 0/0 | 8011 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0028 | 0/0 | 8012 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0031 | 0/0 | 8013 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0032 | 0/0 | 8015 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0033 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0034 | 0/0 | 8012 | 2 | 1 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0035 | 0/0 | 8014 | 2 | 0 | 0 | 1 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8009): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0036 | 0/0 | 8017 | 2 | 1 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0041 | 0/0 | 8021 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8016): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0042 | 0/0 | 8011 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0043 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0044 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0045 | 0/0 | 8011 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0046 | 0/0 | 8012 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0048 | 0/0 | 8012 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0049 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0050 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0051 | 0/0 | 8013 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0052 | 0/0 | 8014 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8009): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0056 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0057 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8011): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0062 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0063 | 0/0 | 8017 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0065 | 0/0 | 8018 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8013): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0066 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0069 | 0/0 | 8013 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0070 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0072 | 0/0 | 8011 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0078 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0081 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0087 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0001t0089 | 0/0 | 8016 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8011): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0003 | 0/0 | 8012 | 44 | 2 | 16 | 11 | 3 | 12 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0004 | 0/0 | 8011 | 2 | 1 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0010 | 0/0 | 8012 | 6 | 0 | 0 | 6 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0012 | 0/0 | 8012 | 4 | 0 | 0 | 4 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0014 | 0/0 | 8014 | 4 | 0 | 4 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8009): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0018 | 0/0 | 8014 | 3 | 0 | 2 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8009): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0025 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0030 | 0/0 | 8012 | 2 | 0 | 2 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0032 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0053 | 0/0 | 8012 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0054 | 0/0 | 8013 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0055 | 0/0 | 8012 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0059 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0061 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0067 | 0/0 | 8016 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8011): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0076 | 0/0 | 8012 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0002t0080 | 0/0 | 8012 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0005 | 0/0 | 8011 | 22 | 0 | 0 | 21 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0022 | 0/0 | 8011 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0068 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0084 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0085 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0003t0086 | 0/0 | 8012 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0004t0001 | 1/0 | 8011 | 1 | 0 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0004t0002 | 0/0 | 8013 | 12 | 1 | 2 | 8 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0004t0006 | 0/0 | 8015 | 3 | 0 | 1 | 1 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0004t0029 | 0/0 | 8013 | 2 | 0 | 1 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0004t0037 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0005t0002 | 0/1 | 8013 | 13 | 2 | 7 | 0 | 2 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0006t0009 | 0/0 | 8013 | 8 | 8 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0006t0077 | 0/0 | 8011 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0006t0079 | 0/0 | 8013 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0007t0002 | 0/0 | 8013 | 6 | 0 | 0 | 6 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0007t0023 | 0/0 | 8013 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0007t0039 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0008t0020 | 0/0 | 8011 | 3 | 0 | 0 | 0 | 0 | 3 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0008t0038 | 0/0 | 8011 | 2 | 0 | 0 | 0 | 0 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0008t0071 | 0/0 | 8013 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0008t0073 | 0/0 | 8015 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0008t0074 | 0/0 | 8015 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0009t0006 | 0/0 | 8015 | 8 | 0 | 5 | 0 | 1 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0010t0013 | 0/0 | 8011 | 4 | 0 | 0 | 4 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0010t0015 | 0/0 | 8011 | 3 | 0 | 2 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0011t0058 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0011t0064 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0013t0047 | 0/0 | 8012 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0014t0040 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0001c0015t0082 | 0/0 | 8013 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0016t0083 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0001c0017t0033 | 0/0 | 8017 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8012): Show |
chr5 | 150503131 | 150563211 |
a0001c0018t0088 | 0/0 | 8012 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0001c0019t0075 | 0/0 | 8013 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0021t0037 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0022t0002 | 0/0 | 8013 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0001c0025t0001 | 0/0 | 8011 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8006): Show |
chr5 | 150503131 | 150563211 |
a0002c0012t0010 | 0/0 | 8012 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8007): Show |
chr5 | 150503131 | 150563211 |
a0003c0026t0060 | 0/0 | 8015 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8010): Show |
chr5 | 150503131 | 150563211 |
a0004c0024t0002 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0005c0020t0002 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
a0006c0023t0002 | 0/0 | 8013 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | CTGGC others(8008): Show |
chr5 | 150503131 | 150563211 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0006 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0011g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0017g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0019g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0019g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0019g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0021g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0024g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0024g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0025g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0026g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0027g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0028g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0028g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0031g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0031g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0032g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0033g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0034g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0034g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0035g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0035g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0036g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0036g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0041g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0042g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0043g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0044g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0045g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0046g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0048g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0049g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0050g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0051g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0052g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0056g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0057g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0062g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0063g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0065g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0066g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0069g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0070g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0072g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0078g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0081g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0087g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0001t0089g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0001 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0005 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0015 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0010g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0010g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0012g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0012g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0012g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0012g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0014g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0014g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0014g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0018g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0018g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0018g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0025g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0030g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0032g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0053g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0054g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0055g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0059g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0061g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0067g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0076g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0002t0080g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0022g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0022g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0068g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0084g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0085g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0003t0086g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0001g0183 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0006g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0006g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0006g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0029g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0029g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0004t0037g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0005t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0009g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0009g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0009g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0077g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0006t0079g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0023g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0023g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0007t0039g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0020g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0020g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0020g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0038g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0038g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0071g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0073g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0008t0074g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0009t0006g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0009t0006g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0009t0006g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0009t0006g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0009t0006g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0013g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0015g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0015g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0010t0015g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0011t0058g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0011t0064g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0013t0047g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0014t0040g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0015t0082g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0016t0083g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0017t0033g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0018t0088g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0019t0075g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0021t0037g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0022t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0001c0025t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0002c0012t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0003c0026t0060g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0004c0024t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0005c0020t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
a0006c0023t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0112 | EUR | GBR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00099 | hp2 | a0001 | c0004 | t0029 | g0169 | EUR | GBR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00280 | hp1 | a0001 | c0010 | t0015 | g0206 | EUR | FIN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0104 | EUR | FIN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00323 | hp1 | a0001 | c0005 | t0002 | g0166 | EUR | FIN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00323 | hp2 | a0001 | c0003 | t0005 | g0051 | EUR | FIN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00438 | hp1 | a0001 | c0004 | t0002 | g0279 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00438 | hp2 | a0001 | c0001 | t0027 | g0027 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00544 | hp1 | a0001 | c0002 | t0012 | g0093 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00544 | hp2 | a0001 | c0004 | t0002 | g0181 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00558 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00558 | hp2 | a0001 | c0004 | t0006 | g0195 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00621 | hp1 | a0001 | c0007 | t0023 | g0222 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00639 | hp1 | a0001 | c0010 | t0015 | g0197 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00642 | hp2 | a0001 | c0009 | t0006 | g0286 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0040 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00673 | hp2 | a0001 | c0003 | t0005 | g0054 | EAS | CHS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0267 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00735 | hp2 | a0001 | c0005 | t0002 | g0010 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00738 | hp1 | a0001 | c0002 | t0030 | g0026 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00738 | hp2 | a0001 | c0004 | t0002 | g0282 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00741 | hp1 | a0001 | c0005 | t0002 | g0193 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0086 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01069 | hp2 | a0001 | c0002 | t0003 | g0087 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01070 | hp1 | a0001 | c0010 | t0015 | g0283 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0015 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01081 | hp1 | a0001 | c0009 | t0006 | g0285 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0239 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0240 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0091 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0310 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01243 | hp1 | a0001 | c0002 | t0076 | g0045 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01243 | hp2 | a0001 | c0001 | t0036 | g0220 | AMR | PUR | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0098 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01255 | hp2 | a0001 | c0005 | t0002 | g0035 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01256 | hp1 | a0001 | c0004 | t0029 | g0228 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01261 | hp1 | a0001 | c0004 | t0002 | g0137 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01346 | hp1 | a0001 | c0002 | t0003 | g0255 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01346 | hp2 | a0001 | c0009 | t0006 | g0013 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0148 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01361 | hp2 | a0001 | c0005 | t0002 | g0142 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0099 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01496 | hp1 | a0001 | c0001 | t0032 | g0334 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01496 | hp2 | a0001 | c0002 | t0030 | g0026 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01515 | hp2 | a0001 | c0009 | t0006 | g0038 | EUR | IBS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01517 | hp2 | a0001 | c0005 | t0002 | g0224 | EUR | IBS | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01884 | hp1 | a0001 | c0006 | t0009 | g0017 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01928 | hp1 | a0001 | c0002 | t0018 | g0327 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01928 | hp2 | a0001 | c0002 | t0003 | g0089 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01934 | hp1 | a0001 | c0002 | t0014 | g0018 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01934 | hp2 | a0001 | c0009 | t0006 | g0013 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01943 | hp1 | a0001 | c0009 | t0006 | g0275 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01952 | hp2 | a0001 | c0002 | t0080 | g0020 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01981 | hp1 | a0001 | c0001 | t0024 | g0296 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01981 | hp2 | a0001 | c0002 | t0014 | g0020 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01993 | hp1 | a0001 | c0005 | t0002 | g0205 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01993 | hp2 | a0001 | c0005 | t0002 | g0170 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02027 | hp1 | a0001 | c0002 | t0010 | g0101 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02040 | hp1 | a0001 | c0004 | t0002 | g0231 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02055 | hp1 | a0001 | c0001 | t0089 | g0113 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02055 | hp2 | a0001 | c0001 | t0028 | g0130 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02056 | hp2 | a0001 | c0002 | t0012 | g0096 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02071 | hp2 | a0001 | c0004 | t0002 | g0194 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02074 | hp1 | a0001 | c0001 | t0026 | g0040 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02074 | hp2 | a0001 | c0003 | t0005 | g0019 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02080 | hp1 | a0001 | c0002 | t0055 | g0109 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02083 | hp1 | a0001 | c0003 | t0022 | g0321 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02129 | hp2 | a0001 | c0007 | t0002 | g0145 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02135 | hp1 | a0001 | c0004 | t0002 | g0230 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02135 | hp2 | a0001 | c0003 | t0005 | g0049 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02145 | hp1 | a0001 | c0001 | t0065 | g0151 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02145 | hp2 | a0001 | c0001 | t0011 | g0241 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02155 | hp2 | a0001 | c0002 | t0012 | g0094 | EAS | CDX | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02165 | hp1 | a0001 | c0004 | t0002 | g0280 | EAS | CDX | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CDX | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02257 | hp1 | a0001 | c0001 | t0062 | g0238 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02258 | hp2 | a0001 | c0001 | t0036 | g0264 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02273 | hp1 | a0001 | c0002 | t0014 | g0066 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02273 | hp2 | a0001 | c0005 | t0002 | g0035 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0138 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02280 | hp2 | a0001 | c0001 | t0008 | g0265 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02293 | hp1 | a0001 | c0004 | t0006 | g0281 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02293 | hp2 | a0001 | c0002 | t0018 | g0245 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02451 | hp1 | a0001 | c0006 | t0009 | g0017 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02451 | hp2 | a0001 | c0001 | t0056 | g0293 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02523 | hp1 | a0001 | c0001 | t0063 | g0009 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02523 | hp2 | a0001 | c0002 | t0012 | g0097 | EAS | KHV | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02572 | hp1 | a0001 | c0005 | t0002 | g0010 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02572 | hp2 | a0001 | c0001 | t0033 | g0273 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0251 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02615 | hp1 | a0001 | c0005 | t0002 | g0010 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02615 | hp2 | a0001 | c0006 | t0077 | g0046 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02622 | hp1 | a0001 | c0002 | t0059 | g0332 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02630 | hp2 | a0001 | c0001 | t0066 | g0152 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02647 | hp1 | a0001 | c0001 | t0051 | g0297 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02647 | hp2 | a0001 | c0011 | t0064 | g0158 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02698 | hp1 | a0001 | c0001 | t0072 | g0036 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02698 | hp2 | a0001 | c0002 | t0053 | g0155 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0335 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02717 | hp2 | a0001 | c0001 | t0019 | g0305 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02723 | hp1 | a0001 | c0001 | t0049 | g0030 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0291 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0005 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02735 | hp2 | a0001 | c0002 | t0003 | g0084 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0092 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02738 | hp2 | a0001 | c0004 | t0006 | g0235 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02809 | hp1 | a0001 | c0006 | t0009 | g0003 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02809 | hp2 | a0001 | c0006 | t0079 | g0047 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02818 | hp1 | a0001 | c0001 | t0016 | g0034 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02886 | hp1 | a0001 | c0001 | t0069 | g0311 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02895 | hp1 | a0001 | c0002 | t0032 | g0127 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02895 | hp2 | a0001 | c0001 | t0034 | g0254 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0294 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02896 | hp2 | a0001 | c0006 | t0009 | g0016 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02897 | hp1 | a0001 | c0006 | t0009 | g0003 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0274 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0174 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02970 | hp2 | a0001 | c0001 | t0070 | g0276 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0024 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03017 | hp2 | a0001 | c0008 | t0071 | g0122 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03041 | hp2 | a0001 | c0006 | t0009 | g0048 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03098 | hp1 | a0001 | c0001 | t0057 | g0146 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03098 | hp2 | a0001 | c0001 | t0052 | g0041 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03130 | hp2 | a0001 | c0011 | t0058 | g0153 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03139 | hp1 | a0001 | c0001 | t0019 | g0330 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03139 | hp2 | a0001 | c0001 | t0008 | g0266 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03209 | hp1 | a0001 | c0001 | t0025 | g0308 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0133 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03225 | hp1 | a0001 | c0006 | t0009 | g0003 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03239 | hp1 | a0001 | c0001 | t0008 | g0252 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03239 | hp2 | a0001 | c0009 | t0006 | g0038 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03453 | hp1 | a0001 | c0001 | t0017 | g0031 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03453 | hp2 | a0001 | c0015 | t0082 | g0081 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03486 | hp1 | a0001 | c0019 | t0075 | g0128 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0207 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0024 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03490 | hp2 | a0001 | c0008 | t0020 | g0123 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03491 | hp2 | a0001 | c0001 | t0042 | g0316 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03492 | hp1 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03492 | hp2 | a0001 | c0008 | t0020 | g0124 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03516 | hp1 | a0001 | c0001 | t0028 | g0132 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03516 | hp2 | a0001 | c0001 | t0016 | g0034 | AFR | ESN | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03540 | hp2 | a0001 | c0013 | t0047 | g0306 | AFR | GWD | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03579 | hp1 | a0001 | c0001 | t0019 | g0219 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03654 | hp1 | a0001 | c0008 | t0038 | g0078 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03654 | hp2 | a0001 | c0008 | t0074 | g0080 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03669 | hp1 | a0001 | c0008 | t0038 | g0082 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03669 | hp2 | a0001 | c0002 | t0054 | g0090 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03688 | hp1 | a0001 | c0008 | t0020 | g0121 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0015 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03704 | hp2 | a0001 | c0009 | t0006 | g0013 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03710 | hp1 | a0001 | c0002 | t0067 | g0095 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03710 | hp2 | a0001 | c0002 | t0003 | g0107 | SAS | PJL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03831 | hp2 | a0002 | c0012 | t0010 | g0100 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0085 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03942 | hp2 | a0001 | c0004 | t0002 | g0196 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04115 | hp1 | a0001 | c0022 | t0002 | g0172 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04115 | hp2 | a0001 | c0001 | t0008 | g0250 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04184 | hp1 | a0001 | c0001 | t0035 | g0165 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04184 | hp2 | a0001 | c0002 | t0018 | g0088 | SAS | BEB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04228 | hp1 | a0001 | c0005 | t0002 | g0192 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG04228 | hp2 | a0001 | c0008 | t0073 | g0079 | SAS | STU | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0136 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18522 | hp2 | a0003 | c0026 | t0060 | g0246 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18612 | hp1 | a0001 | c0001 | t0027 | g0027 | EAS | CHB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18747 | hp2 | a0001 | c0007 | t0039 | g0184 | EAS | CHB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18906 | hp1 | a0001 | c0017 | t0033 | g0215 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0140 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18943 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18943 | hp2 | a0001 | c0003 | t0005 | g0061 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18947 | hp1 | a0001 | c0003 | t0005 | g0059 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18947 | hp2 | a0001 | c0002 | t0010 | g0025 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18948 | hp1 | a0001 | c0003 | t0005 | g0076 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18950 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0161 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18952 | hp2 | a0001 | c0003 | t0022 | g0320 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18953 | hp2 | a0001 | c0007 | t0002 | g0225 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18956 | hp1 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18956 | hp2 | a0001 | c0003 | t0086 | g0022 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18961 | hp2 | a0001 | c0007 | t0023 | g0141 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18962 | hp1 | a0001 | c0003 | t0068 | g0289 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18963 | hp1 | a0001 | c0025 | t0001 | g0247 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18963 | hp2 | a0001 | c0021 | t0037 | g0190 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18964 | hp2 | a0001 | c0004 | t0037 | g0191 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18965 | hp1 | a0001 | c0003 | t0005 | g0056 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18967 | hp2 | a0001 | c0003 | t0005 | g0077 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18968 | hp2 | a0001 | c0003 | t0085 | g0055 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0164 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18970 | hp1 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18971 | hp1 | a0001 | c0007 | t0002 | g0178 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18974 | hp1 | a0001 | c0001 | t0021 | g0072 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18974 | hp2 | a0001 | c0001 | t0078 | g0067 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18975 | hp2 | a0001 | c0004 | t0002 | g0199 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18978 | hp1 | a0001 | c0003 | t0084 | g0064 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18978 | hp2 | a0001 | c0001 | t0035 | g0176 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18979 | hp1 | a0001 | c0010 | t0013 | g0074 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18979 | hp2 | a0001 | c0001 | t0087 | g0065 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18980 | hp1 | a0001 | c0010 | t0013 | g0021 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18982 | hp1 | a0001 | c0016 | t0083 | g0053 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18983 | hp2 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18985 | hp1 | a0001 | c0001 | t0046 | g0139 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18986 | hp1 | a0001 | c0003 | t0005 | g0058 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18990 | hp1 | a0001 | c0007 | t0002 | g0144 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18993 | hp2 | a0001 | c0004 | t0002 | g0200 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18997 | hp1 | a0001 | c0001 | t0034 | g0313 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18997 | hp2 | a0001 | c0003 | t0005 | g0068 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18999 | hp1 | a0001 | c0002 | t0010 | g0001 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19000 | hp1 | a0001 | c0002 | t0004 | g0106 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19000 | hp2 | a0001 | c0010 | t0013 | g0070 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19001 | hp2 | a0001 | c0002 | t0003 | g0236 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19007 | hp1 | a0001 | c0002 | t0003 | g0102 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19010 | hp1 | a0001 | c0010 | t0013 | g0021 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19011 | hp1 | a0001 | c0003 | t0005 | g0050 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19011 | hp2 | a0001 | c0001 | t0031 | g0011 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19012 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19012 | hp2 | a0001 | c0007 | t0002 | g0214 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19030 | hp1 | a0001 | c0002 | t0061 | g0333 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0271 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0295 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19043 | hp2 | a0001 | c0001 | t0008 | g0272 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19056 | hp2 | a0004 | c0024 | t0002 | g0185 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19057 | hp1 | a0001 | c0003 | t0005 | g0052 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19063 | hp1 | a0001 | c0001 | t0021 | g0071 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19063 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19065 | hp1 | a0001 | c0002 | t0010 | g0105 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19065 | hp2 | a0001 | c0003 | t0005 | g0022 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19066 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19067 | hp1 | a0001 | c0001 | t0048 | g0120 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19068 | hp1 | a0001 | c0002 | t0010 | g0025 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19068 | hp2 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19070 | hp1 | a0001 | c0018 | t0088 | g0063 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19074 | hp1 | a0001 | c0003 | t0005 | g0062 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19077 | hp1 | a0005 | c0020 | t0002 | g0298 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19077 | hp2 | a0001 | c0001 | t0021 | g0073 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19078 | hp1 | a0001 | c0003 | t0005 | g0057 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19081 | hp2 | a0001 | c0002 | t0010 | g0001 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19082 | hp1 | a0001 | c0003 | t0005 | g0060 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19082 | hp2 | a0001 | c0001 | t0031 | g0204 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19083 | hp1 | a0001 | c0001 | t0081 | g0069 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19083 | hp2 | a0001 | c0003 | t0005 | g0019 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19084 | hp1 | a0001 | c0003 | t0005 | g0075 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19084 | hp2 | a0001 | c0007 | t0002 | g0180 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19090 | hp2 | a0006 | c0023 | t0002 | g0277 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19240 | hp1 | a0001 | c0014 | t0040 | g0299 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | YRI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ASW | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20129 | hp2 | a0001 | c0001 | t0041 | g0292 | AFR | ASW | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0156 | EUR | TSI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20752 | hp2 | a0001 | c0001 | t0045 | g0002 | EUR | TSI | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20905 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | GIH | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0253 | SAS | GIH | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01123 | hp1 | a0001 | c0002 | t0014 | g0018 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02109 | hp1 | a0001 | c0001 | t0017 | g0031 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0221 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0201 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0232 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG02559 | hp2 | a0001 | c0002 | t0025 | g0217 | AFR | ACB | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03471 | hp1 | a0001 | c0001 | t0050 | g0129 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG03471 | hp2 | a0001 | c0001 | t0044 | g0114 | AFR | MSL | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG06807 | hp1 | a0001 | c0001 | t0043 | g0042 | AFR | USA | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0134 | AFR | USA | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18955 | hp1 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | USA | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA20300 | hp2 | a0001 | c0006 | t0009 | g0016 | AFR | USA | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA21309 | hp1 | a0001 | c0001 | t0024 | g0218 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
homoSapiens | chm13v2 | a0001 | c0005 | t0002 | g0189 | REF | REF | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0183 | REF | REF | NDST1_chr5_150503131_150563211 | NDST1 | chr5 | 150503131 | 150563211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150521294 | G | A | 1 | a0002 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.40G>A | p.Val14Met | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 523/8011 | 40/2649 | 14/882 | chr5 | 150521294 | |||
chr5:150521400 | C | T | 1 | a0003 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.146C>T | p.Ala49Val | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 629/8011 | 146/2649 | 49/882 | chr5 | 150521400 | |||
chr5:150528080 | G | A | 1 | a0005 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.790G>A | p.Ala264Thr | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1273/8011 | 790/2649 | 264/882 | chr5 | 150528080 | |||
chr5:150545461 | C | T | 1 | a0004 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.2120C>T | p.Ala707Val | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/15 | 2603/8011 | 2120/2649 | 707/882 | chr5 | 150545461 | |||
chr5:150551760 | C | T | 1 | a0006 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.2434C>T | p.Pro812Ser | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/15 | 2917/8011 | 2434/2649 | 812/882 | chr5 | 150551760 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150521302 | G | A | 1 | a0001c0013 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.48G>A | p.Pro16Pro | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 531/8011 | 48/2649 | 16/882 | chr5 | 150521302 | |||
chr5:150521602 | G | A | 1 | a0001c0014 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.348G>A | p.Ala116Ala | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 831/8011 | 348/2649 | 116/882 | chr5 | 150521602 | |||
chr5:150527830 | G | A | 1 | a0001c0015 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.540G>A | p.Ala180Ala | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1023/8011 | 540/2649 | 180/882 | chr5 | 150527830 | |||
chr5:150527971 | T | G | 11 | a0001c0002 a0001c0003 a0001c0005 others(8): Show |
139 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
synonymous_variant | LOW | c.681T>G | p.Val227Val | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1164/8011 | 681/2649 | 227/882 | chr5 | 150527971 | |||
chr5:150528040 | A | G | 5 | a0001c0002 a0001c0005 a0001c0008 others(2): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
synonymous_variant | LOW | c.750A>G | p.Pro250Pro | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1233/8011 | 750/2649 | 250/882 | chr5 | 150528040 | |||
chr5:150528079 | C | T | 3 | a0001c0003 a0001c0018 a0001c0025 |
30 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(27): Show |
synonymous_variant | LOW | c.789C>T | p.His263His | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1272/8011 | 789/2649 | 263/882 | chr5 | 150528079 | |||
chr5:150528217 | A | G | 1 | a0001c0008 | 8 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(5): Show |
synonymous_variant | LOW | c.927A>G | p.Pro309Pro | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1410/8011 | 927/2649 | 309/882 | chr5 | 150528217 | |||
chr5:150528256 | C | T | 1 | a0001c0017 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.966C>T | p.Phe322Phe | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/15 | 1449/8011 | 966/2649 | 322/882 | chr5 | 150528256 | |||
chr5:150532965 | C | T | 5 | a0001c0003 a0001c0008 a0001c0010 others(2): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
synonymous_variant | LOW | c.1029C>T | p.Asn343Asn | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/15 | 1512/8011 | 1029/2649 | 343/882 | chr5 | 150532965 | |||
chr5:150535762 | C | T | 1 | a0001c0013 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1314C>T | p.Pro438Pro | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/15 | 1797/8011 | 1314/2649 | 438/882 | chr5 | 150535762 | |||
chr5:150535840 | G | A | 1 | a0001c0021 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1392G>A | p.Leu464Leu | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/15 | 1875/8011 | 1392/2649 | 464/882 | chr5 | 150535840 | |||
chr5:150540177 | G | C | 20 | a0001c0001 a0001c0002 a0001c0003 others(17): Show |
347 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(344): Show |
synonymous_variant | LOW | c.1662G>C | p.Thr554Thr | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/15 | 2145/8011 | 1662/2649 | 554/882 | chr5 | 150540177 | |||
chr5:150540211 | T | C | 1 | a0001c0022 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1696T>C | p.Leu566Leu | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/15 | 2179/8011 | 1696/2649 | 566/882 | chr5 | 150540211 | |||
chr5:150540216 | G | A | 1 | a0001c0009 | 8 | HG00642.hp2 HG01081.hp1 HG01346.hp2 others(5): Show |
synonymous_variant | LOW | c.1701G>A | p.Ala567Ala | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/15 | 2184/8011 | 1701/2649 | 567/882 | chr5 | 150540216 | |||
chr5:150549782 | C | T | 1 | a0001c0011 | 2 | HG02647.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.2421C>T | p.Thr807Thr | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/15 | 2904/8011 | 2421/2649 | 807/882 | chr5 | 150549782 | |||
chr5:150553260 | C | T | 2 | a0001c0007 a0004c0024 |
10 | HG00621.hp1 HG02129.hp2 NA18747.hp2 others(7): Show |
synonymous_variant | LOW | c.2577C>T | p.Leu859Leu | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3060/8011 | 2577/2649 | 859/882 | chr5 | 150553260 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150508171 | A | G | 23 | a0001c0001t0021 a0001c0001t0078 a0001c0001t0081 others(20): Show |
60 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(57): Show |
5_prime_UTR_variant | MODIFIER | c.-443A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/15 | 13084 | chr5 | 150508171 | ||||||
chr5:150508182 | C | T | 2 | a0001c0004t0037 a0001c0021t0037 |
2 | NA18963.hp2 NA18964.hp2 |
5_prime_UTR_variant | MODIFIER | c.-432C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/15 | 13073 | chr5 | 150508182 | ||||||
chr5:150520952 | C | T | 1 | a0001c0001t0072 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-303C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 303 | chr5 | 150520952 | ||||||
chr5:150521049 | C | T | 3 | a0001c0008t0020 a0001c0008t0038 a0001c0008t0071 |
6 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-206C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 206 | chr5 | 150521049 | ||||||
chr5:150521240 | G | T | 13 | a0001c0001t0019 a0001c0001t0036 a0001c0001t0069 others(10): Show |
37 | HG00323.hp2 HG00673.hp2 HG01243.hp2 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-15G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/15 | 15 | chr5 | 150521240 | ||||||
chr5:150553372 | G | A | 15 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(12): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*40G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 40 | chr5 | 150553372 | ||||||
chr5:150553434 | G | A | 14 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(11): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*102G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 102 | chr5 | 150553434 | ||||||
chr5:150553646 | G | A | 1 | a0001c0007t0039 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 314 | chr5 | 150553646 | ||||||
chr5:150553660 | C | G | 13 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(10): Show |
43 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*328C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 328 | chr5 | 150553660 | ||||||
chr5:150553686 | G | C | 1 | a0001c0002t0076 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*354G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 354 | chr5 | 150553686 | ||||||
chr5:150553729 | C | T | 1 | a0001c0015t0082 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 397 | chr5 | 150553729 | ||||||
chr5:150553812 | C | A | 2 | a0001c0001t0041 a0001c0014t0040 |
2 | NA19240.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*480C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 480 | chr5 | 150553812 | ||||||
chr5:150553836 | G | A | 1 | a0001c0007t0023 | 2 | HG00621.hp1 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*504G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 504 | chr5 | 150553836 | ||||||
chr5:150553968 | C | T | 1 | a0001c0019t0075 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*636C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 636 | chr5 | 150553968 | ||||||
chr5:150554279 | G | GT | 4 | a0001c0001t0034 a0001c0001t0035 a0001c0001t0081 others(1): Show |
6 | HG02895.hp2 HG04184.hp1 NA18956.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*958dupT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 959 | INFO_REALIGN_3_PRIME | chr5 | 150554279 | |||||
chr5:150554335 | T | TTA | 37 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0016 others(34): Show |
171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1026_*1027dupTA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1028 | INFO_REALIGN_3_PRIME | chr5 | 150554335 | |||||
chr5:150554335 | T | TTATA | 18 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0032 others(15): Show |
36 | HG00558.hp2 HG00642.hp2 HG01081.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1024_*1027dupTATA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1028 | INFO_REALIGN_3_PRIME | chr5 | 150554335 | |||||
chr5:150554335 | T | TTATATA | 10 | a0001c0001t0033 a0001c0001t0036 a0001c0001t0062 others(7): Show |
11 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1027dupTATA others(2): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1028 | INFO_REALIGN_3_PRIME | chr5 | 150554335 | |||||
chr5:150554335 | T | TTATATAT others(3): Show |
1 | a0001c0001t0041 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018_*1027dupTATA others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1028 | INFO_REALIGN_3_PRIME | chr5 | 150554335 | |||||
chr5:150554449 | C | T | 1 | a0001c0002t0055 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1117C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1117 | chr5 | 150554449 | ||||||
chr5:150554474 | G | A | 2 | a0001c0001t0011 a0001c0001t0051 |
7 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1142G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1142 | chr5 | 150554474 | ||||||
chr5:150554475 | G | A | 1 | a0001c0001t0070 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1143G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1143 | chr5 | 150554475 | ||||||
chr5:150554544 | G | T | 4 | a0001c0001t0007 a0001c0001t0028 a0001c0001t0049 others(1): Show |
16 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1212G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1212 | chr5 | 150554544 | ||||||
chr5:150554551 | G | A | 1 | a0001c0001t0042 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1219 | chr5 | 150554551 | ||||||
chr5:150554564 | C | T | 2 | a0001c0001t0069 a0001c0006t0009 |
9 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1232C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1232 | chr5 | 150554564 | ||||||
chr5:150554595 | G | A | 1 | a0001c0001t0049 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1263G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1263 | chr5 | 150554595 | ||||||
chr5:150554630 | G | A | 1 | a0001c0006t0079 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1298G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1298 | chr5 | 150554630 | ||||||
chr5:150554632 | G | A | 1 | a0001c0008t0073 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1300G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1300 | chr5 | 150554632 | ||||||
chr5:150554698 | G | C | 1 | a0001c0003t0084 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1366G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1366 | chr5 | 150554698 | ||||||
chr5:150554785 | A | T | 1 | a0001c0001t0048 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1453A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1453 | chr5 | 150554785 | ||||||
chr5:150555236 | G | A | 4 | a0001c0001t0007 a0001c0001t0028 a0001c0001t0049 others(1): Show |
16 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1904G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1904 | chr5 | 150555236 | ||||||
chr5:150555285 | G | A | 1 | a0001c0001t0050 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1953G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 1953 | chr5 | 150555285 | ||||||
chr5:150555382 | A | C | 12 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(9): Show |
42 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2050A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2050 | chr5 | 150555382 | ||||||
chr5:150555478 | T | A | 9 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0036 others(6): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2146T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2146 | chr5 | 150555478 | ||||||
chr5:150555490 | G | A | 1 | a0001c0001t0043 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2158G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2158 | chr5 | 150555490 | ||||||
chr5:150555609 | T | C | 45 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(42): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2277 | chr5 | 150555609 | ||||||
chr5:150555813 | G | A | 1 | a0001c0001t0045 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2481G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2481 | chr5 | 150555813 | ||||||
chr5:150555816 | G | A | 1 | a0001c0019t0075 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2484G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2484 | chr5 | 150555816 | ||||||
chr5:150555987 | G | A | 9 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0036 others(6): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2655G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2655 | chr5 | 150555987 | ||||||
chr5:150556002 | G | C | 1 | a0001c0001t0004 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2670G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2670 | chr5 | 150556002 | ||||||
chr5:150556071 | C | T | 1 | a0001c0002t0076 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2739C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2739 | chr5 | 150556071 | ||||||
chr5:150556118 | A | G | 14 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0012 others(11): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2786A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2786 | chr5 | 150556118 | ||||||
chr5:150556232 | A | G | 1 | a0001c0002t0061 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2900A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2900 | chr5 | 150556232 | ||||||
chr5:150556331 | T | C | 1 | a0001c0004t0029 | 2 | HG00099.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2999T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 2999 | chr5 | 150556331 | ||||||
chr5:150556606 | T | C | 15 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(12): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3274T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3274 | chr5 | 150556606 | ||||||
chr5:150556758 | G | A | 1 | a0001c0003t0022 | 2 | HG02083.hp1 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3426G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3426 | chr5 | 150556758 | ||||||
chr5:150556772 | A | G | 1 | a0001c0001t0027 | 2 | HG00438.hp2 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3440A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3440 | chr5 | 150556772 | ||||||
chr5:150556846 | G | A | 7 | a0001c0001t0004 a0001c0001t0027 a0001c0001t0031 others(4): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3514G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3514 | chr5 | 150556846 | ||||||
chr5:150556859 | C | T | 1 | a0001c0001t0026 | 2 | HG00673.hp1 HG02074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3527C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3527 | chr5 | 150556859 | ||||||
chr5:150556960 | G | C | 5 | a0001c0001t0025 a0001c0001t0032 a0001c0002t0025 others(2): Show |
5 | HG01496.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3628G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3628 | chr5 | 150556960 | ||||||
chr5:150557016 | G | A | 14 | a0001c0003t0005 a0001c0003t0022 a0001c0003t0068 others(11): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3684G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3684 | chr5 | 150557016 | ||||||
chr5:150557047 | C | G | 1 | a0001c0001t0044 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3715C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3715 | chr5 | 150557047 | ||||||
chr5:150557066 | A | G | 9 | a0001c0001t0019 a0001c0001t0024 a0001c0001t0036 others(6): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3734A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3734 | chr5 | 150557066 | ||||||
chr5:150557126 | C | T | 2 | a0001c0002t0010 a0002c0012t0010 |
7 | HG02027.hp1 HG03831.hp2 NA18947.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3794C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3794 | chr5 | 150557126 | ||||||
chr5:150557268 | A | G | 2 | a0001c0006t0079 a0001c0015t0082 |
2 | HG02809.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3936A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3936 | chr5 | 150557268 | ||||||
chr5:150557278 | G | T | 3 | a0001c0001t0016 a0001c0001t0065 a0001c0001t0066 |
5 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3946G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 3946 | chr5 | 150557278 | ||||||
chr5:150557379 | C | T | 2 | a0001c0011t0058 a0001c0011t0064 |
2 | HG02647.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4047C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4047 | chr5 | 150557379 | ||||||
chr5:150557609 | T | G | 1 | a0001c0002t0053 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4277T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4277 | chr5 | 150557609 | ||||||
chr5:150557675 | T | C | 3 | a0001c0002t0012 a0001c0002t0055 a0001c0002t0067 |
6 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4343T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4343 | chr5 | 150557675 | ||||||
chr5:150557933 | TA | T | 14 | a0001c0002t0003 a0001c0002t0010 a0001c0002t0012 others(11): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*4602delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4602 | chr5 | 150557933 | ||||||
chr5:150558074 | G | A | 1 | a0001c0001t0041 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4742G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4742 | chr5 | 150558074 | ||||||
chr5:150558080 | A | G | 1 | a0001c0003t0085 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4748A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4748 | chr5 | 150558080 | ||||||
chr5:150558081 | G | A | 1 | a0001c0003t0085 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4749G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4749 | chr5 | 150558081 | ||||||
chr5:150558082 | A | AG | 10 | a0001c0001t0028 a0001c0001t0046 a0001c0001t0048 others(7): Show |
11 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4755dupG | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4756 | INFO_REALIGN_3_PRIME | chr5 | 150558082 | |||||
chr5:150558082 | A | G | 1 | a0001c0003t0085 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4750A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4750 | chr5 | 150558082 | ||||||
chr5:150558177 | G | A | 33 | a0001c0001t0017 a0001c0002t0003 a0001c0002t0010 others(30): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*4845G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 15/15 | 4845 | chr5 | 150558177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150508322 | A | AGT | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(105): Show |
122 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.-388+125_-388+126d others(4): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508322 | A | AGTGT | 25 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
27 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(24): Show |
intron_variant | MODIFIER | c.-388+123_-388+126d others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508322 | A | AGTGTGTG others(9): Show |
2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-388+111_-388+126d others(18): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508322 | A | AGTGTGTG others(11): Show |
2 | a0001c0001t0032g0334 a0001c0002t0004g0335 |
2 | HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-388+109_-388+126d others(20): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508322 | AGT | A | 15 | a0001c0001t0001g0125 a0001c0001t0002g0006 a0001c0001t0002g0126 others(12): Show |
18 | HG01069.hp1 HG01071.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.-388+125_-388+126d others(4): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508322 | AGTGT | A | 38 | a0001c0001t0027g0027 a0001c0002t0003g0001 a0001c0002t0003g0005 others(35): Show |
49 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.-388+123_-388+126d others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508322 | ||||||
chr5:150508341 | G | GTGTGTGG others(2): Show |
49 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(46): Show |
58 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.-388+121_-388+122i others(11): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508341 | ||||||
chr5:150508341 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0089g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-388+123_-388+124i others(13): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150508341 | ||||||
chr5:150508386 | T | C | 7 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(4): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-388+160T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508386 | |||||||
chr5:150508436 | G | A | 1 | a0001c0001t0089g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-388+210G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508436 | |||||||
chr5:150508439 | A | T | 1 | a0001c0008t0038g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-388+213A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508439 | |||||||
chr5:150508482 | T | C | 2 | a0001c0002t0025g0217 a0001c0002t0032g0127 |
2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-388+256T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508482 | |||||||
chr5:150508509 | G | A | 41 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(38): Show |
46 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.-388+283G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508509 | |||||||
chr5:150508825 | C | G | 1 | a0001c0001t0001g0044 | 2 | NA18945.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-388+599C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508825 | |||||||
chr5:150508852 | C | G | 1 | a0001c0002t0003g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-388+626C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508852 | |||||||
chr5:150508953 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-388+727C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508953 | |||||||
chr5:150508954 | G | A | 46 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(43): Show |
51 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.-388+728G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150508954 | |||||||
chr5:150509274 | G | C | 39 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(36): Show |
44 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.-388+1048G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509274 | |||||||
chr5:150509336 | A | G | 1 | a0001c0001t0001g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-388+1110A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509336 | |||||||
chr5:150509374 | T | C | 9 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(6): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-388+1148T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509374 | |||||||
chr5:150509398 | C | T | 1 | a0001c0002t0003g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-388+1172C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509398 | |||||||
chr5:150509399 | G | A | 12 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(9): Show |
15 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.-388+1173G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509399 | |||||||
chr5:150509468 | G | A | 1 | a0001c0004t0002g0137 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-388+1242G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509468 | |||||||
chr5:150509520 | C | G | 1 | a0001c0002t0003g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-388+1294C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509520 | |||||||
chr5:150509794 | C | A | 1 | a0001c0008t0073g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-388+1568C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509794 | |||||||
chr5:150509795 | C | T | 1 | a0001c0001t0025g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-388+1569C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509795 | |||||||
chr5:150509798 | T | C | 55 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(52): Show |
64 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(61): Show |
intron_variant | MODIFIER | c.-388+1572T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509798 | |||||||
chr5:150509848 | G | A | 2 | a0001c0001t0017g0031 a0001c0001t0017g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-388+1622G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509848 | |||||||
chr5:150509869 | T | A | 1 | a0001c0001t0089g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-388+1643T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509869 | |||||||
chr5:150509925 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0072g0036 |
2 | HG00642.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-388+1699G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509925 | |||||||
chr5:150509974 | C | T | 1 | a0001c0001t0089g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-388+1748C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150509974 | |||||||
chr5:150510180 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-388+1954C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510180 | |||||||
chr5:150510205 | C | T | 2 | a0001c0008t0038g0078 a0001c0008t0038g0082 |
2 | HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-388+1979C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510205 | |||||||
chr5:150510231 | C | G | 5 | a0001c0003t0005g0022 a0001c0003t0005g0075 a0001c0003t0005g0076 others(2): Show |
5 | NA18948.hp1 NA18956.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.-388+2005C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510231 | |||||||
chr5:150510272 | G | A | 1 | a0001c0001t0046g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-388+2046G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510272 | |||||||
chr5:150510279 | A | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-388+2053A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510279 | |||||||
chr5:150510426 | T | C | 7 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(4): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-388+2200T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510426 | |||||||
chr5:150510433 | C | T | 42 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(39): Show |
47 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.-388+2207C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510433 | |||||||
chr5:150510440 | A | G | 1 | a0001c0001t0004g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-388+2214A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510440 | |||||||
chr5:150510508 | TGTCCCGT others(18): Show |
T | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-388+2284_-388+230 others(29): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150510508 | ||||||
chr5:150510906 | A | G | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-388+2680A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510906 | |||||||
chr5:150510977 | C | A | 9 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(6): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-388+2751C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150510977 | |||||||
chr5:150511243 | C | G | 1 | a0001c0013t0047g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-388+3017C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511243 | |||||||
chr5:150511243 | C | T | 7 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(4): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-388+3017C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511243 | |||||||
chr5:150511368 | G | C | 4 | a0001c0001t0019g0219 a0001c0001t0036g0220 a0001c0001t0069g0311 others(1): Show |
4 | HG01243.hp2 HG02886.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-388+3142G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511368 | |||||||
chr5:150511515 | A | G | 9 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(6): Show |
13 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-388+3289A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511515 | |||||||
chr5:150511538 | C | T | 5 | a0001c0001t0002g0041 a0001c0001t0019g0305 a0001c0001t0019g0330 others(2): Show |
5 | HG02015.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-388+3312C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511538 | |||||||
chr5:150511545 | A | G | 1 | a0001c0002t0055g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-388+3319A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511545 | |||||||
chr5:150511553 | G | A | 8 | a0001c0002t0076g0045 a0001c0006t0009g0003 a0001c0006t0009g0016 others(5): Show |
12 | HG01243.hp1 HG01884.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-388+3327G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511553 | |||||||
chr5:150511614 | C | G | 1 | a0001c0001t0002g0304 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-388+3388C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511614 | |||||||
chr5:150511700 | G | A | 4 | a0001c0001t0032g0334 a0001c0002t0004g0335 a0001c0002t0059g0332 others(1): Show |
4 | HG01496.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-388+3474G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511700 | |||||||
chr5:150511755 | T | C | 4 | a0001c0001t0032g0334 a0001c0002t0004g0335 a0001c0002t0059g0332 others(1): Show |
4 | HG01496.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-388+3529T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511755 | |||||||
chr5:150511794 | C | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0126 |
4 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-388+3568C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511794 | |||||||
chr5:150511821 | G | A | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-388+3595G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511821 | |||||||
chr5:150511957 | TG | T | 39 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(36): Show |
44 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.-388+3732delG | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150511957 | |||||||
chr5:150512164 | A | G | 6 | a0001c0001t0001g0044 a0001c0001t0001g0300 a0001c0001t0001g0301 others(3): Show |
7 | HG02129.hp1 NA18612.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-388+3938A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512164 | |||||||
chr5:150512167 | C | A | 44 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(41): Show |
49 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.-388+3941C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512167 | |||||||
chr5:150512342 | G | T | 1 | a0001c0014t0040g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-388+4116G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512342 | |||||||
chr5:150512381 | A | G | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-388+4155A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512381 | |||||||
chr5:150512437 | C | T | 1 | a0001c0007t0002g0214 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-388+4211C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512437 | |||||||
chr5:150512504 | G | T | 39 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(36): Show |
44 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.-388+4278G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512504 | |||||||
chr5:150512506 | A | T | 39 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(36): Show |
44 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.-388+4280A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512506 | |||||||
chr5:150512527 | T | G | 1 | a0001c0001t0011g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-388+4301T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512527 | |||||||
chr5:150512553 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0017g0031 a0001c0001t0017g0138 |
4 | HG02083.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-388+4327G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512553 | |||||||
chr5:150512721 | A | G | 42 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(39): Show |
47 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.-388+4495A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512721 | |||||||
chr5:150512958 | T | C | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-388+4732T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150512958 | |||||||
chr5:150513119 | G | A | 3 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0044g0114 |
5 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-388+4893G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513119 | |||||||
chr5:150513156 | C | T | 7 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(4): Show |
8 | NA18974.hp1 NA18979.hp1 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.-388+4930C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513156 | |||||||
chr5:150513161 | C | T | 12 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(9): Show |
15 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.-388+4935C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513161 | |||||||
chr5:150513188 | C | T | 1 | a0001c0001t0004g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-388+4962C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513188 | |||||||
chr5:150513377 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(245): Show |
288 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.-388+5151A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513377 | |||||||
chr5:150513399 | G | A | 4 | a0001c0001t0019g0219 a0001c0001t0036g0220 a0001c0001t0069g0311 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-388+5173G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513399 | |||||||
chr5:150513617 | A | G | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-388+5391A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513617 | |||||||
chr5:150513725 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(123): Show |
142 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.-388+5499C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513725 | |||||||
chr5:150513810 | C | T | 39 | a0001c0001t0027g0027 a0001c0002t0003g0001 a0001c0002t0003g0005 others(36): Show |
50 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.-388+5584C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513810 | |||||||
chr5:150513849 | C | G | 1 | a0001c0010t0015g0206 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-388+5623C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513849 | |||||||
chr5:150513917 | G | C | 1 | a0001c0001t0011g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-388+5691G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150513917 | |||||||
chr5:150514038 | G | A | 1 | a0001c0001t0016g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-388+5812G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514038 | |||||||
chr5:150514089 | A | T | 4 | a0001c0001t0002g0041 a0001c0001t0019g0305 a0001c0001t0019g0330 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-388+5863A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514089 | |||||||
chr5:150514178 | G | C | 13 | a0001c0002t0003g0005 a0001c0002t0003g0023 a0001c0002t0003g0083 others(10): Show |
16 | HG00099.hp1 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-388+5952G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514178 | |||||||
chr5:150514186 | T | C | 26 | a0001c0001t0027g0027 a0001c0002t0003g0001 a0001c0002t0003g0024 others(23): Show |
34 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.-388+5960T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514186 | |||||||
chr5:150514335 | C | T | 4 | a0001c0001t0026g0040 a0001c0005t0002g0035 a0001c0005t0002g0205 others(1): Show |
6 | HG00673.hp1 HG01255.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-388+6109C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514335 | |||||||
chr5:150514336 | G | A | 2 | a0001c0004t0002g0230 a0001c0004t0002g0231 |
2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-388+6110G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514336 | |||||||
chr5:150514386 | A | G | 8 | a0001c0001t0011g0229 a0001c0001t0011g0291 a0001c0001t0011g0294 others(5): Show |
8 | HG01884.hp2 HG01981.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-388+6160A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514386 | |||||||
chr5:150514492 | C | T | 45 | a0001c0001t0019g0219 a0001c0001t0021g0071 a0001c0001t0021g0072 others(42): Show |
50 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.-388+6266C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514492 | |||||||
chr5:150514560 | C | CA | 18 | a0001c0001t0001g0208 a0001c0001t0001g0233 a0001c0001t0001g0234 others(15): Show |
19 | HG01123.hp2 HG02027.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-387-6286dupA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150514560 | ||||||
chr5:150514560 | CA | C | 29 | a0001c0001t0001g0288 a0001c0001t0001g0290 a0001c0001t0002g0202 others(26): Show |
35 | HG00558.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-387-6286delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150514560 | ||||||
chr5:150514582 | A | AT | 3 | a0001c0001t0081g0069 a0001c0002t0014g0018 a0001c0010t0013g0070 |
4 | HG01123.hp1 HG01934.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-387-6286_-387-628 others(5): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514582 | |||||||
chr5:150514582 | A | T | 34 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(31): Show |
38 | HG00323.hp2 HG00673.hp2 HG01952.hp2 others(35): Show |
intron_variant | MODIFIER | c.-387-6286A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514582 | |||||||
chr5:150514801 | G | A | 2 | a0001c0007t0023g0141 a0001c0007t0023g0222 |
2 | HG00621.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-387-6067G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150514801 | |||||||
chr5:150515055 | G | A | 1 | a0001c0001t0050g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-387-5813G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515055 | |||||||
chr5:150515068 | G | T | 4 | a0001c0001t0019g0219 a0001c0001t0036g0220 a0001c0001t0069g0311 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-387-5800G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515068 | |||||||
chr5:150515324 | A | G | 68 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(65): Show |
81 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(78): Show |
intron_variant | MODIFIER | c.-387-5544A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515324 | |||||||
chr5:150515517 | G | C | 1 | a0001c0001t0004g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-387-5351G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515517 | |||||||
chr5:150515585 | C | T | 31 | a0001c0001t0078g0067 a0001c0001t0087g0065 a0001c0002t0014g0018 others(28): Show |
34 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-387-5283C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515585 | |||||||
chr5:150515782 | C | T | 10 | a0001c0002t0003g0005 a0001c0002t0003g0023 a0001c0002t0003g0083 others(7): Show |
13 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-387-5086C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515782 | |||||||
chr5:150515836 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-387-5032C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515836 | |||||||
chr5:150515837 | G | A | 2 | a0001c0002t0076g0045 a0001c0006t0077g0046 |
2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-387-5031G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515837 | |||||||
chr5:150515854 | G | A | 2 | a0001c0005t0002g0142 a0001c0005t0002g0224 |
2 | HG01361.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-387-5014G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515854 | |||||||
chr5:150515911 | T | G | 1 | a0001c0006t0079g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-387-4957T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515911 | |||||||
chr5:150515930 | T | C | 274 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(271): Show |
314 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.-387-4938T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150515930 | |||||||
chr5:150516012 | C | T | 1 | a0001c0008t0038g0082 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-387-4856C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516012 | |||||||
chr5:150516140 | T | C | 13 | a0001c0001t0002g0041 a0001c0001t0017g0031 a0001c0001t0017g0138 others(10): Show |
14 | HG01243.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-387-4728T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516140 | |||||||
chr5:150516184 | A | C | 8 | a0001c0004t0002g0230 a0001c0004t0002g0231 a0001c0004t0002g0279 others(5): Show |
8 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.-387-4684A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516184 | |||||||
chr5:150516760 | G | C | 1 | a0001c0001t0081g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-387-4108G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516760 | |||||||
chr5:150516918 | G | T | 18 | a0001c0001t0001g0043 a0001c0001t0001g0125 a0001c0001t0001g0211 others(15): Show |
19 | HG01928.hp1 HG02004.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.-387-3950G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516918 | |||||||
chr5:150516946 | G | C | 2 | a0001c0002t0003g0236 a0001c0002t0003g0237 |
2 | NA18956.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-387-3922G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150516946 | |||||||
chr5:150516976 | A | AGT | 38 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(35): Show |
41 | HG01361.hp2 HG01496.hp1 HG01517.hp2 others(38): Show |
intron_variant | MODIFIER | c.-387-3851_-387-385 others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | A | AGTGT | 30 | a0001c0001t0001g0303 a0001c0001t0002g0041 a0001c0001t0002g0167 others(27): Show |
34 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.-387-3853_-387-385 others(8): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | A | AGTGTGT | 10 | a0001c0001t0002g0175 a0001c0001t0004g0118 a0001c0001t0011g0291 others(7): Show |
11 | HG01255.hp2 HG01256.hp1 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.-387-3855_-387-385 others(10): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0011g0221 a0001c0001t0011g0229 a0001c0001t0011g0295 others(2): Show |
5 | HG01884.hp2 HG01981.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-387-3857_-387-385 others(12): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0051g0297 a0001c0004t0002g0201 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-387-3859_-387-385 others(14): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGT | A | 49 | a0001c0001t0001g0037 a0001c0001t0001g0248 a0001c0001t0001g0249 others(46): Show |
55 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.-387-3851_-387-385 others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGT | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0209 others(8): Show |
15 | HG01099.hp2 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-387-3853_-387-385 others(8): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGTGT | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0044g0114 others(3): Show |
8 | HG00438.hp1 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-387-3855_-387-385 others(10): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGTGTG others(1): Show |
A | 5 | a0001c0003t0005g0068 a0001c0008t0038g0078 a0001c0008t0038g0082 others(2): Show |
5 | HG03654.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-387-3857_-387-385 others(12): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGTGTG others(3): Show |
A | 38 | a0001c0001t0002g0143 a0001c0001t0011g0241 a0001c0001t0019g0219 others(35): Show |
43 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.-387-3859_-387-385 others(14): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGTGTG others(5): Show |
A | 6 | a0001c0002t0003g0111 a0001c0002t0030g0026 a0001c0002t0076g0045 others(3): Show |
10 | HG00738.hp1 HG01243.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-387-3861_-387-385 others(16): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150516976 | AGTGTGTG others(7): Show |
A | 42 | a0001c0001t0062g0238 a0001c0002t0003g0001 a0001c0002t0003g0005 others(39): Show |
53 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-387-3863_-387-385 others(18): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150516976 | ||||||
chr5:150517304 | A | AT | 19 | a0001c0001t0001g0234 a0001c0001t0004g0216 a0001c0001t0004g0227 others(16): Show |
22 | HG00438.hp1 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-387-3549dupT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150517304 | ||||||
chr5:150517304 | AT | A | 97 | a0001c0001t0001g0242 a0001c0001t0001g0256 a0001c0001t0007g0007 others(94): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.-387-3549delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150517304 | ||||||
chr5:150517523 | C | T | 43 | a0001c0001t0062g0238 a0001c0002t0003g0001 a0001c0002t0003g0005 others(40): Show |
55 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-387-3345C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517523 | |||||||
chr5:150517596 | C | T | 2 | a0001c0008t0038g0078 a0001c0008t0038g0082 |
2 | HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-387-3272C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517596 | |||||||
chr5:150517621 | T | C | 116 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(113): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-387-3247T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517621 | |||||||
chr5:150517663 | G | C | 30 | a0001c0001t0078g0067 a0001c0001t0087g0065 a0001c0002t0014g0018 others(27): Show |
34 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-387-3205G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517663 | |||||||
chr5:150517729 | T | G | 116 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(113): Show |
140 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-387-3139T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517729 | |||||||
chr5:150517858 | G | A | 1 | a0001c0002t0053g0155 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-387-3010G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150517858 | |||||||
chr5:150518096 | G | C | 1 | a0001c0007t0002g0178 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-387-2772G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518096 | |||||||
chr5:150518189 | AC | A | 36 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(33): Show |
40 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.-387-2678delC | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518189 | |||||||
chr5:150518246 | C | G | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-387-2622C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518246 | |||||||
chr5:150518378 | G | A | 1 | a0001c0001t0001g0319 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-387-2490G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518378 | |||||||
chr5:150518415 | C | T | 1 | a0001c0002t0012g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-387-2453C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518415 | |||||||
chr5:150518471 | A | G | 1 | a0001c0014t0040g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-387-2397A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518471 | |||||||
chr5:150518473 | A | G | 1 | a0001c0001t0002g0173 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-387-2395A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518473 | |||||||
chr5:150518649 | G | A | 6 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-387-2219G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518649 | |||||||
chr5:150518685 | A | G | 1 | a0001c0001t0007g0136 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-387-2183A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518685 | |||||||
chr5:150518783 | CT | C | 76 | a0001c0001t0004g0033 a0001c0001t0004g0179 a0001c0001t0004g0188 others(73): Show |
93 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-387-2073delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150518783 | ||||||
chr5:150518816 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0007g0131 a0001c0001t0007g0135 others(2): Show |
6 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-387-2052G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518816 | |||||||
chr5:150518838 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-387-2030G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518838 | |||||||
chr5:150518937 | C | T | 2 | a0001c0002t0003g0023 a0001c0002t0003g0087 |
3 | HG01069.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-387-1931C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518937 | |||||||
chr5:150518948 | T | C | 30 | a0001c0001t0078g0067 a0001c0001t0087g0065 a0001c0002t0014g0018 others(27): Show |
34 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-387-1920T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150518948 | |||||||
chr5:150519044 | TG | T | 71 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(68): Show |
87 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.-387-1821delG | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150519044 | ||||||
chr5:150519155 | G | C | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-387-1713G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519155 | |||||||
chr5:150519323 | T | A | 1 | a0001c0008t0020g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-387-1545T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519323 | |||||||
chr5:150519383 | CCTT | C | 30 | a0001c0001t0078g0067 a0001c0001t0087g0065 a0001c0002t0014g0018 others(27): Show |
34 | HG00323.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.-387-1482_-387-148 others(7): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150519383 | ||||||
chr5:150519434 | G | A | 1 | a0001c0003t0005g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-387-1434G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519434 | |||||||
chr5:150519565 | G | A | 1 | a0003c0026t0060g0246 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-387-1303G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519565 | |||||||
chr5:150519636 | C | T | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-387-1232C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519636 | |||||||
chr5:150519830 | C | T | 2 | a0001c0001t0032g0334 a0001c0002t0004g0335 |
2 | HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-387-1038C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519830 | |||||||
chr5:150519831 | G | C | 1 | a0001c0002t0003g0232 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-387-1037G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519831 | |||||||
chr5:150519847 | G | A | 1 | a0001c0001t0044g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-387-1021G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519847 | |||||||
chr5:150519907 | G | A | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-387-961G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519907 | |||||||
chr5:150519920 | G | A | 2 | a0001c0009t0006g0285 a0001c0009t0006g0286 |
2 | HG00642.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.-387-948G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519920 | |||||||
chr5:150519974 | G | C | 5 | a0001c0001t0002g0147 a0001c0002t0003g0098 a0001c0002t0003g0099 others(2): Show |
6 | HG00738.hp1 HG01255.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.-387-894G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150519974 | |||||||
chr5:150520083 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0126 a0001c0001t0044g0114 |
5 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-387-785C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520083 | |||||||
chr5:150520129 | G | A | 1 | a0001c0004t0002g0280 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-387-739G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520129 | |||||||
chr5:150520236 | G | C | 2 | a0001c0001t0017g0031 a0001c0001t0017g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-387-632G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520236 | |||||||
chr5:150520274 | G | A | 74 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(71): Show |
82 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.-387-594G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520274 | |||||||
chr5:150520330 | CAGA | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-536_-387-534d others(5): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 150520330 | ||||||
chr5:150520336 | G | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-532G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520336 | |||||||
chr5:150520337 | A | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-531A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520337 | |||||||
chr5:150520338 | A | C | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-530A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520338 | |||||||
chr5:150520339 | A | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-529A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520339 | |||||||
chr5:150520340 | A | T | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-528A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520340 | |||||||
chr5:150520341 | GACT | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(225): Show |
263 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.-387-526_-387-524d others(5): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520341 | |||||||
chr5:150520406 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-387-462C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520406 | |||||||
chr5:150520418 | G | A | 2 | a0001c0002t0003g0085 a0001c0002t0018g0088 |
2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-387-450G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520418 | |||||||
chr5:150520439 | G | A | 2 | a0001c0006t0077g0046 a0001c0017t0033g0215 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-387-429G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520439 | |||||||
chr5:150520579 | A | C | 14 | a0001c0001t0007g0030 a0001c0001t0007g0133 a0001c0001t0007g0134 others(11): Show |
14 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-387-289A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520579 | |||||||
chr5:150520708 | T | C | 1 | a0001c0003t0005g0051 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-387-160T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520708 | |||||||
chr5:150520765 | C | T | 1 | a0001c0001t0004g0187 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-387-103C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520765 | |||||||
chr5:150520860 | C | T | 2 | a0001c0002t0025g0217 a0001c0002t0032g0127 |
2 | HG02559.hp2 HG02895.hp1 |
splice_region_variant&intron_variant | LOW | c.-387-8C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 1/14 | chr5 | 150520860 | |||||||
chr5:150521811 | G | C | 105 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0001t0019g0219 others(102): Show |
122 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.513+44G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150521811 | |||||||
chr5:150521825 | G | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0149 |
2 | HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.513+58G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150521825 | |||||||
chr5:150521845 | G | A | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+78G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150521845 | |||||||
chr5:150521971 | CA | C | 2 | a0001c0001t0017g0031 a0001c0001t0017g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.513+205delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150521971 | |||||||
chr5:150521982 | C | T | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+215C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150521982 | |||||||
chr5:150522174 | G | C | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.513+407G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522174 | |||||||
chr5:150522272 | A | G | 56 | a0001c0001t0001g0039 a0001c0001t0001g0263 a0001c0001t0004g0198 others(53): Show |
70 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.513+505A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522272 | |||||||
chr5:150522282 | T | A | 2 | a0001c0004t0002g0279 a0001c0004t0002g0280 |
2 | HG00438.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.513+515T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522282 | |||||||
chr5:150522402 | C | G | 1 | a0001c0002t0003g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.513+635C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522402 | |||||||
chr5:150522410 | G | A | 16 | a0001c0001t0019g0219 a0001c0001t0036g0220 a0001c0001t0036g0264 others(13): Show |
17 | HG01243.hp2 HG01255.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+643G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522410 | |||||||
chr5:150522431 | G | T | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.513+664G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522431 | |||||||
chr5:150522440 | G | A | 1 | a0001c0001t0001g0257 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.513+673G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522440 | |||||||
chr5:150522440 | G | C | 3 | a0001c0001t0002g0041 a0001c0001t0052g0041 a0001c0002t0003g0107 |
3 | HG02922.hp1 HG03098.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.513+673G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522440 | |||||||
chr5:150522496 | G | A | 2 | a0001c0001t0004g0117 a0001c0001t0004g0179 |
2 | NA18983.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.513+729G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522496 | |||||||
chr5:150522549 | A | C | 1 | a0001c0001t0004g0028 | 2 | NA18954.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.513+782A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522549 | |||||||
chr5:150522683 | G | A | 30 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(27): Show |
33 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(30): Show |
intron_variant | MODIFIER | c.513+916G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522683 | |||||||
chr5:150522762 | A | G | 1 | a0001c0002t0061g0333 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.513+995A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522762 | |||||||
chr5:150522769 | CAGAG | C | 4 | a0001c0001t0011g0294 a0001c0001t0024g0296 a0001c0001t0041g0292 others(1): Show |
4 | HG01981.hp1 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1003_513+1006d others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522769 | |||||||
chr5:150522773 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(91): Show |
105 | HG00280.hp1 HG00621.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.513+1006G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522773 | |||||||
chr5:150522906 | C | T | 14 | a0001c0001t0002g0009 a0001c0001t0002g0159 a0001c0001t0002g0160 others(11): Show |
16 | HG02080.hp2 HG02165.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.513+1139C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522906 | |||||||
chr5:150522997 | C | T | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+1230C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150522997 | |||||||
chr5:150523151 | A | C | 8 | a0001c0008t0020g0121 a0001c0008t0020g0123 a0001c0008t0020g0124 others(5): Show |
8 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+1384A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523151 | |||||||
chr5:150523286 | G | C | 1 | a0001c0003t0005g0052 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.513+1519G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523286 | |||||||
chr5:150523323 | C | A | 1 | a0001c0001t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.513+1556C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523323 | |||||||
chr5:150523361 | T | C | 3 | a0001c0001t0024g0218 a0001c0014t0040g0299 a0001c0019t0075g0128 |
3 | HG03486.hp1 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.513+1594T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523361 | |||||||
chr5:150523375 | A | G | 1 | a0001c0004t0002g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.513+1608A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523375 | |||||||
chr5:150523443 | C | T | 6 | a0001c0008t0020g0121 a0001c0008t0020g0123 a0001c0008t0020g0124 others(3): Show |
6 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+1676C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523443 | |||||||
chr5:150523568 | A | G | 68 | a0001c0001t0024g0218 a0001c0001t0032g0334 a0001c0002t0003g0001 others(65): Show |
81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.513+1801A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523568 | |||||||
chr5:150523599 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.513+1832C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523599 | |||||||
chr5:150523694 | G | C | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.513+1927G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523694 | |||||||
chr5:150523754 | T | C | 1 | a0001c0001t0042g0316 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.513+1987T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523754 | |||||||
chr5:150523788 | G | T | 5 | a0001c0001t0024g0218 a0001c0002t0059g0332 a0001c0002t0061g0333 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2021G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523788 | |||||||
chr5:150523980 | A | T | 2 | a0001c0001t0019g0305 a0001c0001t0019g0330 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.513+2213A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150523980 | |||||||
chr5:150524117 | C | G | 1 | a0001c0001t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.513+2350C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524117 | |||||||
chr5:150524296 | C | T | 1 | a0001c0001t0008g0253 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.513+2529C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524296 | |||||||
chr5:150524297 | G | T | 58 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.513+2530G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524297 | |||||||
chr5:150524346 | C | T | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.513+2579C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524346 | |||||||
chr5:150524443 | G | A | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+2676G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524443 | |||||||
chr5:150524487 | C | T | 1 | a0001c0002t0003g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.513+2720C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524487 | |||||||
chr5:150524562 | G | A | 1 | a0001c0002t0003g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.513+2795G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524562 | |||||||
chr5:150524573 | A | G | 5 | a0001c0001t0024g0218 a0001c0002t0059g0332 a0001c0002t0061g0333 others(2): Show |
5 | HG02622.hp1 HG03486.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2806A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524573 | |||||||
chr5:150524639 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.513+2872G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524639 | |||||||
chr5:150524672 | A | G | 63 | a0001c0001t0032g0334 a0001c0002t0003g0001 a0001c0002t0003g0005 others(60): Show |
76 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.513+2905A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524672 | |||||||
chr5:150524685 | G | T | 2 | a0001c0006t0077g0046 a0001c0017t0033g0215 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.513+2918G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524685 | |||||||
chr5:150524721 | G | A | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.513+2954G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524721 | |||||||
chr5:150524733 | G | A | 27 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(24): Show |
30 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.513+2966G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524733 | |||||||
chr5:150524914 | T | C | 13 | a0001c0001t0024g0218 a0001c0002t0059g0332 a0001c0002t0061g0333 others(10): Show |
13 | HG02622.hp1 HG03017.hp2 HG03486.hp1 others(10): Show |
intron_variant | MODIFIER | c.514-2890T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524914 | |||||||
chr5:150524930 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.514-2874C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150524930 | |||||||
chr5:150525027 | A | G | 1 | a0001c0002t0003g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.514-2777A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525027 | |||||||
chr5:150525132 | G | A | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.514-2672G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525132 | |||||||
chr5:150525134 | G | A | 33 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(30): Show |
36 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.514-2670G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525134 | |||||||
chr5:150525137 | T | C | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-2667T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525137 | |||||||
chr5:150525450 | T | C | 8 | a0001c0008t0020g0121 a0001c0008t0020g0123 a0001c0008t0020g0124 others(5): Show |
8 | HG03017.hp2 HG03490.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-2354T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525450 | |||||||
chr5:150525480 | C | T | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.514-2324C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525480 | |||||||
chr5:150525697 | C | T | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-2107C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525697 | |||||||
chr5:150525729 | G | A | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.514-2075G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525729 | |||||||
chr5:150525735 | G | A | 1 | a0001c0001t0021g0071 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.514-2069G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150525735 | |||||||
chr5:150526071 | C | T | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.514-1733C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526071 | |||||||
chr5:150526183 | G | A | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.514-1621G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526183 | |||||||
chr5:150526320 | A | G | 1 | a0001c0014t0040g0299 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.514-1484A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526320 | |||||||
chr5:150526440 | C | T | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-1364C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526440 | |||||||
chr5:150526542 | C | T | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.514-1262C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526542 | |||||||
chr5:150526609 | A | G | 27 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(24): Show |
30 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.514-1195A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526609 | |||||||
chr5:150526761 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.514-1043T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526761 | |||||||
chr5:150526770 | C | T | 2 | a0001c0002t0059g0332 a0001c0002t0061g0333 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.514-1034C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526770 | |||||||
chr5:150526786 | A | C | 64 | a0001c0001t0032g0334 a0001c0002t0003g0001 a0001c0002t0003g0005 others(61): Show |
77 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.514-1018A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526786 | |||||||
chr5:150526825 | GGAAGGTC others(2): Show |
G | 3 | a0001c0001t0032g0334 a0001c0002t0025g0217 a0001c0002t0032g0127 |
3 | HG01496.hp1 HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.514-973_514-965del others(9): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 150526825 | ||||||
chr5:150526958 | G | A | 67 | a0001c0001t0032g0334 a0001c0002t0003g0001 a0001c0002t0003g0005 others(64): Show |
80 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.514-846G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150526958 | |||||||
chr5:150527160 | C | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.514-644C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150527160 | |||||||
chr5:150527452 | G | C | 15 | a0001c0001t0002g0041 a0001c0001t0007g0007 a0001c0001t0007g0029 others(12): Show |
18 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-352G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150527452 | |||||||
chr5:150527479 | C | T | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.514-325C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150527479 | |||||||
chr5:150527641 | G | A | 33 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(30): Show |
36 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(33): Show |
intron_variant | MODIFIER | c.514-163G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150527641 | |||||||
chr5:150527663 | G | T | 1 | a0001c0010t0015g0206 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.514-141G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 2/14 | chr5 | 150527663 | |||||||
chr5:150528609 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(255): Show |
299 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1008+311A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528609 | |||||||
chr5:150528619 | C | T | 1 | a0001c0002t0003g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1008+321C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528619 | |||||||
chr5:150528621 | T | G | 3 | a0001c0005t0002g0166 a0001c0005t0002g0192 a0001c0005t0002g0193 |
3 | HG00323.hp1 HG00741.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1008+323T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528621 | |||||||
chr5:150528664 | G | A | 61 | a0001c0001t0032g0334 a0001c0002t0003g0001 a0001c0002t0003g0005 others(58): Show |
74 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1008+366G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528664 | |||||||
chr5:150528747 | A | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+449A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528747 | |||||||
chr5:150528970 | T | C | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1008+672T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150528970 | |||||||
chr5:150529045 | G | A | 5 | a0001c0001t0008g0014 a0001c0001t0008g0265 a0001c0001t0008g0271 others(2): Show |
7 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+747G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529045 | |||||||
chr5:150529113 | C | T | 65 | a0001c0001t0025g0308 a0001c0001t0032g0334 a0001c0002t0003g0001 others(62): Show |
78 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1008+815C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529113 | |||||||
chr5:150529117 | T | A | 26 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(23): Show |
29 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1008+819T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529117 | |||||||
chr5:150529150 | G | T | 1 | a0001c0001t0011g0294 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1008+852G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529150 | |||||||
chr5:150529164 | G | A | 13 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0001t0019g0219 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+866G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529164 | |||||||
chr5:150529170 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1008+872T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529170 | |||||||
chr5:150529203 | G | C | 64 | a0001c0001t0025g0308 a0001c0001t0032g0334 a0001c0002t0003g0001 others(61): Show |
77 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1008+905G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529203 | |||||||
chr5:150529241 | A | G | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1008+943A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529241 | |||||||
chr5:150529390 | C | CA | 111 | a0001c0001t0001g0125 a0001c0001t0001g0234 a0001c0001t0001g0268 others(108): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.1008+1115dupA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150529390 | ||||||
chr5:150529390 | C | CAA | 25 | a0001c0001t0008g0271 a0001c0001t0025g0308 a0001c0001t0032g0334 others(22): Show |
25 | HG00544.hp1 HG00673.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1008+1114_1008+111 others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150529390 | ||||||
chr5:150529390 | CA | C | 8 | a0001c0001t0001g0212 a0001c0001t0001g0233 a0001c0001t0002g0147 others(5): Show |
8 | HG02055.hp1 HG02922.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.1008+1115delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150529390 | ||||||
chr5:150529390 | CAA | C | 13 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0001t0019g0219 others(10): Show |
14 | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+1114_1008+111 others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150529390 | ||||||
chr5:150529412 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1008+1114A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529412 | |||||||
chr5:150529522 | T | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+1224T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529522 | |||||||
chr5:150529570 | C | T | 1 | a0001c0002t0014g0066 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1008+1272C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529570 | |||||||
chr5:150529696 | C | T | 13 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(10): Show |
16 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1008+1398C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529696 | |||||||
chr5:150529835 | G | A | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1008+1537G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529835 | |||||||
chr5:150529870 | G | A | 1 | a0005c0020t0002g0298 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1008+1572G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529870 | |||||||
chr5:150529872 | A | G | 1 | a0001c0002t0012g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1008+1574A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529872 | |||||||
chr5:150529879 | G | A | 35 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(32): Show |
38 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1008+1581G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529879 | |||||||
chr5:150529957 | G | C | 1 | a0001c0004t0037g0191 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1008+1659G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529957 | |||||||
chr5:150529992 | G | A | 13 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0001t0019g0219 others(10): Show |
14 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+1694G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150529992 | |||||||
chr5:150530052 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1008+1754C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530052 | |||||||
chr5:150530152 | G | C | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+1854G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530152 | |||||||
chr5:150530192 | T | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+1894T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530192 | |||||||
chr5:150530214 | TGCTGCTT others(3): Show |
T | 3 | a0001c0002t0012g0094 a0001c0002t0012g0097 a0001c0002t0067g0095 |
3 | HG02155.hp2 HG02523.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1008+1925_1008+193 others(14): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530214 | ||||||
chr5:150530369 | C | T | 87 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0001t0019g0219 others(84): Show |
105 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.1008+2071C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530369 | |||||||
chr5:150530447 | G | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1008+2149G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530447 | |||||||
chr5:150530513 | A | G | 1 | a0001c0002t0003g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1008+2215A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530513 | |||||||
chr5:150530557 | A | AT | 22 | a0001c0001t0001g0211 a0001c0001t0001g0234 a0001c0001t0002g0149 others(19): Show |
24 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1008+2283dupT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530557 | ||||||
chr5:150530557 | AT | A | 17 | a0001c0001t0001g0248 a0001c0001t0001g0331 a0001c0001t0004g0117 others(14): Show |
20 | HG01081.hp1 HG01358.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1008+2283delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530557 | ||||||
chr5:150530557 | ATT | A | 39 | a0001c0001t0007g0287 a0001c0001t0017g0031 a0001c0001t0017g0138 others(36): Show |
43 | HG00323.hp2 HG00673.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.1008+2282_1008+228 others(6): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530557 | ||||||
chr5:150530557 | ATTTT | A | 3 | a0001c0006t0009g0003 a0001c0006t0009g0016 a0001c0006t0009g0017 |
7 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1008+2280_1008+228 others(8): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530557 | ||||||
chr5:150530557 | ATTTTTTT others(4): Show |
A | 68 | a0001c0001t0025g0308 a0001c0001t0032g0334 a0001c0002t0003g0001 others(65): Show |
81 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1008+2273_1008+228 others(15): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150530557 | ||||||
chr5:150530600 | G | C | 1 | a0001c0001t0001g0269 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1008+2302G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530600 | |||||||
chr5:150530774 | G | A | 2 | a0001c0001t0017g0031 a0001c0001t0017g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1009-2171G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530774 | |||||||
chr5:150530810 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1009-2135T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530810 | |||||||
chr5:150530840 | A | C | 59 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(56): Show |
72 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1009-2105A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530840 | |||||||
chr5:150530842 | G | A | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1009-2103G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530842 | |||||||
chr5:150530889 | A | G | 13 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(10): Show |
16 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1009-2056A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530889 | |||||||
chr5:150530963 | G | A | 64 | a0001c0001t0025g0308 a0001c0001t0032g0334 a0001c0002t0003g0001 others(61): Show |
77 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.1009-1982G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150530963 | |||||||
chr5:150531144 | C | T | 2 | a0001c0004t0002g0230 a0001c0004t0002g0231 |
2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1009-1801C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531144 | |||||||
chr5:150531171 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1009-1774A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531171 | |||||||
chr5:150531199 | A | G | 1 | a0001c0001t0016g0140 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1009-1746A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531199 | |||||||
chr5:150531267 | C | T | 2 | a0001c0008t0073g0079 a0001c0008t0074g0080 |
2 | HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1009-1678C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531267 | |||||||
chr5:150531323 | C | T | 4 | a0001c0002t0004g0106 a0001c0002t0010g0025 a0001c0002t0010g0101 others(1): Show |
5 | HG02027.hp1 NA18947.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1009-1622C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531323 | |||||||
chr5:150531424 | T | C | 103 | a0001c0001t0001g0043 a0001c0001t0001g0125 a0001c0001t0001g0211 others(100): Show |
123 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1009-1521T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531424 | |||||||
chr5:150531457 | T | C | 3 | a0001c0001t0007g0131 a0001c0001t0024g0218 a0001c0001t0028g0130 |
3 | HG02055.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1009-1488T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531457 | |||||||
chr5:150531500 | C | CTTTTTTT | 33 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(30): Show |
36 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1009-1434_1009-142 others(11): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150531500 | ||||||
chr5:150531500 | CT | C | 64 | a0001c0001t0001g0243 a0001c0001t0002g0160 a0001c0001t0002g0175 others(61): Show |
77 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1009-1428delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150531500 | ||||||
chr5:150531531 | A | G | 2 | a0001c0004t0006g0235 a0001c0004t0006g0281 |
2 | HG02293.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1009-1414A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531531 | |||||||
chr5:150531657 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(223): Show |
261 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.1009-1288A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531657 | |||||||
chr5:150531798 | G | A | 1 | a0001c0003t0068g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1009-1147G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531798 | |||||||
chr5:150531924 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(108): Show |
126 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1009-1021G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531924 | |||||||
chr5:150531929 | G | A | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1009-1016G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150531929 | |||||||
chr5:150532092 | A | G | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1009-853A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532092 | |||||||
chr5:150532108 | G | C | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1009-837G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532108 | |||||||
chr5:150532231 | C | T | 1 | a0001c0002t0018g0088 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1009-714C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532231 | |||||||
chr5:150532300 | T | C | 1 | a0001c0001t0006g0174 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1009-645T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532300 | |||||||
chr5:150532414 | G | A | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1009-531G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532414 | |||||||
chr5:150532502 | C | A | 58 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1009-443C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532502 | |||||||
chr5:150532525 | CT | C | 116 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(113): Show |
137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1009-410delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr5 | 150532525 | ||||||
chr5:150532646 | C | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0288 a0001c0025t0001g0247 |
3 | HG00621.hp2 NA18954.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1009-299C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532646 | |||||||
chr5:150532802 | C | T | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1009-143C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532802 | |||||||
chr5:150532864 | G | A | 1 | a0001c0002t0003g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1009-81G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 3/14 | chr5 | 150532864 | |||||||
chr5:150533037 | G | A | 1 | a0001c0004t0006g0281 | 1 | HG02293.hp1 | splice_region_variant&intron_variant | LOW | c.1096+5G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533037 | |||||||
chr5:150533050 | T | G | 1 | a0001c0001t0021g0072 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1096+18T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533050 | |||||||
chr5:150533125 | G | A | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1096+93G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533125 | |||||||
chr5:150533126 | T | C | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1096+94T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533126 | |||||||
chr5:150533177 | A | G | 42 | a0001c0002t0004g0335 a0001c0003t0005g0004 a0001c0003t0005g0019 others(39): Show |
46 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1096+145A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533177 | |||||||
chr5:150533200 | A | G | 119 | a0001c0001t0004g0117 a0001c0001t0004g0179 a0001c0001t0019g0219 others(116): Show |
140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1096+168A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533200 | |||||||
chr5:150533266 | C | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(70): Show |
82 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1096+234C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533266 | |||||||
chr5:150533650 | A | G | 2 | a0001c0001t0004g0119 a0001c0001t0048g0120 |
2 | NA18965.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1096+618A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533650 | |||||||
chr5:150533781 | A | T | 1 | a0001c0001t0004g0216 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1096+749A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533781 | |||||||
chr5:150533785 | T | A | 68 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(65): Show |
76 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1096+753T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533785 | |||||||
chr5:150533795 | A | G | 12 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(9): Show |
12 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1096+763A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533795 | |||||||
chr5:150533940 | C | T | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1096+908C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533940 | |||||||
chr5:150533944 | G | A | 6 | a0001c0001t0069g0311 a0001c0006t0009g0003 a0001c0006t0009g0016 others(3): Show |
10 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+912G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150533944 | |||||||
chr5:150534037 | C | T | 13 | a0001c0001t0007g0007 a0001c0001t0007g0029 a0001c0001t0007g0030 others(10): Show |
16 | HG02055.hp2 HG02486.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1097-830C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150534037 | |||||||
chr5:150534120 | G | A | 117 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(114): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1097-747G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150534120 | |||||||
chr5:150534341 | C | T | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1097-526C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150534341 | |||||||
chr5:150534664 | C | T | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097-203C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150534664 | |||||||
chr5:150534839 | T | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(257): Show |
300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.1097-28T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 4/14 | chr5 | 150534839 | |||||||
chr5:150535049 | C | T | 1 | a0001c0002t0003g0112 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1251+28C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535049 | |||||||
chr5:150535054 | C | T | 1 | a0001c0007t0002g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1251+33C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535054 | |||||||
chr5:150535069 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(107): Show |
125 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(122): Show |
intron_variant | MODIFIER | c.1251+48G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535069 | |||||||
chr5:150535227 | G | T | 5 | a0001c0001t0069g0311 a0001c0006t0009g0003 a0001c0006t0009g0016 others(2): Show |
9 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1251+206G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535227 | |||||||
chr5:150535433 | T | C | 1 | a0001c0002t0003g0102 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1252-267T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535433 | |||||||
chr5:150535464 | G | A | 1 | a0001c0005t0002g0224 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1252-236G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535464 | |||||||
chr5:150535532 | A | G | 4 | a0001c0001t0016g0034 a0001c0001t0016g0140 a0001c0001t0065g0151 others(1): Show |
5 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1252-168A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535532 | |||||||
chr5:150535578 | T | G | 68 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(65): Show |
76 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1252-122T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535578 | |||||||
chr5:150535587 | A | G | 1 | a0001c0001t0017g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1252-113A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535587 | |||||||
chr5:150535624 | C | T | 5 | a0001c0003t0005g0022 a0001c0003t0005g0075 a0001c0003t0005g0076 others(2): Show |
5 | NA18948.hp1 NA18956.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.1252-76C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 5/14 | chr5 | 150535624 | |||||||
chr5:150536114 | C | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(299): Show |
349 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(346): Show |
intron_variant | MODIFIER | c.1437+229C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536114 | |||||||
chr5:150536203 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1437+318T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536203 | |||||||
chr5:150536207 | T | C | 1 | a0001c0002t0003g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1437+322T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536207 | |||||||
chr5:150536347 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1437+462T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536347 | |||||||
chr5:150536374 | T | C | 5 | a0001c0001t0007g0029 a0001c0001t0007g0131 a0001c0001t0007g0135 others(2): Show |
6 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1437+489T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536374 | |||||||
chr5:150536438 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(66): Show |
77 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1437+553C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536438 | |||||||
chr5:150536505 | CA | C | 6 | a0001c0001t0069g0311 a0001c0006t0009g0003 a0001c0006t0009g0016 others(3): Show |
10 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1437+634delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 150536505 | ||||||
chr5:150536519 | A | AAT | 27 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(24): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
intron_variant | MODIFIER | c.1437+634_1437+635i others(4): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536519 | |||||||
chr5:150536519 | A | AT | 39 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(36): Show |
43 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1437+643dupT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 150536519 | ||||||
chr5:150536578 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(108): Show |
126 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1437+693T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536578 | |||||||
chr5:150536729 | A | C | 68 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(65): Show |
76 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1437+844A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536729 | |||||||
chr5:150536784 | C | T | 2 | a0001c0001t0017g0031 a0001c0001t0017g0138 |
3 | HG02109.hp1 HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1437+899C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536784 | |||||||
chr5:150536915 | G | A | 9 | a0001c0008t0020g0121 a0001c0008t0020g0123 a0001c0008t0020g0124 others(6): Show |
9 | HG00280.hp1 HG00639.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1437+1030G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536915 | |||||||
chr5:150536963 | C | T | 1 | a0001c0004t0002g0196 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1437+1078C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150536963 | |||||||
chr5:150537114 | T | C | 1 | a0001c0003t0068g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1437+1229T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537114 | |||||||
chr5:150537138 | G | A | 1 | a0001c0002t0010g0105 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1437+1253G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537138 | |||||||
chr5:150537154 | G | A | 1 | a0001c0001t0050g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1437+1269G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537154 | |||||||
chr5:150537156 | G | A | 1 | a0001c0002t0003g0091 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1437+1271G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537156 | |||||||
chr5:150537166 | C | T | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1437+1281C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537166 | |||||||
chr5:150537167 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1437+1282G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537167 | |||||||
chr5:150537308 | C | T | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1437+1423C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537308 | |||||||
chr5:150537365 | G | A | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1437+1480G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537365 | |||||||
chr5:150537374 | T | C | 9 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1437+1489T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537374 | |||||||
chr5:150537385 | A | G | 68 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(65): Show |
76 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1437+1500A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537385 | |||||||
chr5:150537511 | G | C | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1437+1626G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537511 | |||||||
chr5:150537753 | C | T | 10 | a0001c0001t0008g0014 a0001c0001t0008g0265 a0001c0001t0008g0266 others(7): Show |
12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1438-1475C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537753 | |||||||
chr5:150537799 | T | A | 1 | a0001c0004t0002g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1438-1429T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537799 | |||||||
chr5:150537813 | A | G | 68 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(65): Show |
76 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1438-1415A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537813 | |||||||
chr5:150537841 | G | C | 1 | a0001c0001t0057g0146 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1438-1387G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537841 | |||||||
chr5:150537951 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1438-1277A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150537951 | |||||||
chr5:150538041 | A | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1438-1187A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538041 | |||||||
chr5:150538089 | C | T | 5 | a0001c0001t0019g0305 a0001c0001t0019g0330 a0001c0001t0036g0220 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1438-1139C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538089 | |||||||
chr5:150538114 | A | C | 5 | a0001c0003t0005g0049 a0001c0003t0005g0050 a0001c0010t0013g0021 others(2): Show |
6 | HG02135.hp2 NA18979.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1438-1114A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538114 | |||||||
chr5:150538228 | C | T | 58 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1438-1000C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538228 | |||||||
chr5:150538236 | G | T | 1 | a0001c0013t0047g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1438-992G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538236 | |||||||
chr5:150538670 | G | A | 6 | a0001c0001t0011g0221 a0001c0001t0011g0229 a0001c0001t0011g0291 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1438-558G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538670 | |||||||
chr5:150538827 | C | T | 27 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(24): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
intron_variant | MODIFIER | c.1438-401C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150538827 | |||||||
chr5:150539051 | C | T | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1438-177C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150539051 | |||||||
chr5:150539109 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1438-119C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150539109 | |||||||
chr5:150539136 | G | C | 2 | a0001c0003t0022g0320 a0001c0003t0022g0321 |
2 | HG02083.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1438-92G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150539136 | |||||||
chr5:150539138 | G | A | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1438-90G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150539138 | |||||||
chr5:150539187 | C | A | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0328 others(1): Show |
4 | HG02004.hp2 HG02300.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1438-41C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 6/14 | chr5 | 150539187 | |||||||
chr5:150539498 | A | G | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG01952.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1566+142A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150539498 | |||||||
chr5:150539671 | A | G | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1566+315A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150539671 | |||||||
chr5:150539909 | G | A | 9 | a0001c0003t0005g0022 a0001c0003t0005g0056 a0001c0003t0005g0075 others(6): Show |
9 | HG02083.hp1 NA18948.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.1567-173G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150539909 | |||||||
chr5:150539944 | G | T | 1 | a0001c0002t0003g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1567-138G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150539944 | |||||||
chr5:150540023 | G | A | 1 | a0001c0005t0002g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1567-59G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150540023 | |||||||
chr5:150540030 | G | A | 1 | a0001c0001t0008g0250 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1567-52G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 7/14 | chr5 | 150540030 | |||||||
chr5:150540542 | G | A | 1 | a0001c0005t0002g0193 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1749+278G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150540542 | |||||||
chr5:150540686 | C | T | 1 | a0001c0001t0034g0313 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1749+422C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150540686 | |||||||
chr5:150540721 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1749+457T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150540721 | |||||||
chr5:150540873 | G | A | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1749+609G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150540873 | |||||||
chr5:150541022 | G | T | 1 | a0001c0002t0025g0217 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1750-548G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541022 | |||||||
chr5:150541029 | G | A | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1750-541G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541029 | |||||||
chr5:150541313 | T | A | 1 | a0001c0004t0029g0169 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1750-257T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541313 | |||||||
chr5:150541537 | G | C | 1 | a0001c0003t0005g0057 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1750-33G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541537 | |||||||
chr5:150541538 | C | G | 1 | a0001c0003t0005g0057 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1750-32C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541538 | |||||||
chr5:150541539 | G | C | 1 | a0001c0003t0005g0057 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1750-31G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 8/14 | chr5 | 150541539 | |||||||
chr5:150541689 | G | C | 146 | a0001c0001t0002g0041 a0001c0001t0004g0011 a0001c0001t0004g0028 others(143): Show |
171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1846+23G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150541689 | |||||||
chr5:150541708 | C | A | 2 | a0001c0001t0036g0220 a0001c0001t0062g0238 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1846+42C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150541708 | |||||||
chr5:150541894 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0052g0041 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1846+228G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150541894 | |||||||
chr5:150541939 | G | A | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1846+273G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150541939 | |||||||
chr5:150542449 | C | T | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1847-399C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150542449 | |||||||
chr5:150542646 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(71): Show |
83 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1847-202C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150542646 | |||||||
chr5:150542695 | C | T | 4 | a0001c0001t0016g0034 a0001c0001t0016g0140 a0001c0001t0065g0151 others(1): Show |
5 | HG02145.hp1 HG02630.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1847-153C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150542695 | |||||||
chr5:150542764 | C | T | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1847-84C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150542764 | |||||||
chr5:150542826 | C | T | 1 | a0001c0002t0004g0106 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1847-22C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 9/14 | chr5 | 150542826 | |||||||
chr5:150542981 | C | T | 1 | a0001c0001t0024g0218 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1970+10C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150542981 | |||||||
chr5:150542996 | C | T | 6 | a0001c0002t0012g0093 a0001c0002t0012g0094 a0001c0002t0012g0096 others(3): Show |
6 | HG00544.hp1 HG02056.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970+25C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150542996 | |||||||
chr5:150543001 | C | T | 2 | a0001c0001t0004g0028 a0001c0001t0004g0118 |
3 | NA18954.hp2 NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1970+30C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543001 | |||||||
chr5:150543054 | C | G | 2 | a0001c0002t0003g0092 a0001c0002t0003g0104 |
2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1970+83C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543054 | |||||||
chr5:150543075 | C | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0288 a0001c0025t0001g0247 |
3 | HG00621.hp2 NA18954.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1970+104C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543075 | |||||||
chr5:150543081 | T | G | 1 | a0001c0015t0082g0081 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1970+110T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543081 | |||||||
chr5:150543358 | G | A | 38 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(35): Show |
42 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1970+387G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543358 | |||||||
chr5:150543390 | G | A | 2 | a0001c0002t0003g0024 a0001c0002t0003g0107 |
3 | HG03017.hp1 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1970+419G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543390 | |||||||
chr5:150543431 | G | A | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1970+460G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543431 | |||||||
chr5:150543616 | A | G | 27 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(24): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
intron_variant | MODIFIER | c.1970+645A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543616 | |||||||
chr5:150543636 | T | A | 1 | a0001c0005t0002g0205 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1970+665T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543636 | |||||||
chr5:150543647 | C | T | 66 | a0001c0001t0002g0041 a0001c0001t0052g0041 a0001c0001t0069g0311 others(63): Show |
83 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1970+676C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543647 | |||||||
chr5:150543783 | CT | C | 7 | a0001c0001t0001g0256 a0001c0001t0002g0175 a0001c0001t0004g0227 others(4): Show |
7 | HG02040.hp1 NA18941.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1970+826delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr5 | 150543783 | ||||||
chr5:150543799 | A | G | 58 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1970+828A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543799 | |||||||
chr5:150543848 | C | T | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1970+877C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543848 | |||||||
chr5:150543849 | G | A | 2 | a0001c0001t0008g0251 a0001c0001t0008g0253 |
2 | HG02602.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1970+878G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543849 | |||||||
chr5:150543874 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0322 |
2 | NA18940.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1970+903G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543874 | |||||||
chr5:150543928 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1970+957C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543928 | |||||||
chr5:150543979 | C | T | 6 | a0001c0001t0002g0009 a0001c0001t0002g0160 a0001c0001t0002g0163 others(3): Show |
7 | HG02080.hp2 HG02165.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1970+1008C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543979 | |||||||
chr5:150543980 | A | T | 1 | a0001c0001t0004g0188 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1970+1009A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543980 | |||||||
chr5:150543986 | G | C | 1 | a0001c0007t0002g0144 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1970+1015G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150543986 | |||||||
chr5:150544024 | C | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1970+1053C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544024 | |||||||
chr5:150544025 | G | A | 5 | a0001c0001t0024g0218 a0001c0001t0041g0292 a0001c0008t0073g0079 others(2): Show |
5 | HG03654.hp2 HG04228.hp2 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.1970+1054G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544025 | |||||||
chr5:150544086 | A | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1970+1115A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544086 | |||||||
chr5:150544283 | C | T | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.1971-1029C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544283 | |||||||
chr5:150544352 | TG | T | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1971-959delG | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544352 | |||||||
chr5:150544406 | G | A | 58 | a0001c0002t0003g0001 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
71 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.1971-906G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544406 | |||||||
chr5:150544447 | G | A | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1971-865G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544447 | |||||||
chr5:150544449 | C | G | 1 | a0001c0017t0033g0215 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1971-863C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544449 | |||||||
chr5:150544628 | C | T | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1971-684C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544628 | |||||||
chr5:150544641 | C | A | 2 | a0001c0001t0002g0041 a0001c0001t0052g0041 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1971-671C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544641 | |||||||
chr5:150544725 | T | C | 1 | a0001c0002t0003g0089 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1971-587T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544725 | |||||||
chr5:150544755 | G | A | 1 | a0001c0003t0005g0075 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1971-557G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544755 | |||||||
chr5:150544951 | G | C | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1971-361G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544951 | |||||||
chr5:150544953 | G | A | 4 | a0001c0001t0017g0031 a0001c0001t0017g0138 a0001c0006t0079g0047 others(1): Show |
5 | HG02109.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1971-359G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150544953 | |||||||
chr5:150545055 | C | T | 1 | a0001c0004t0002g0181 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1971-257C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150545055 | |||||||
chr5:150545237 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1971-75C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 10/14 | chr5 | 150545237 | |||||||
chr5:150545663 | G | T | 1 | a0001c0007t0039g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2145+177G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150545663 | |||||||
chr5:150545748 | T | C | 1 | a0001c0002t0003g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2145+262T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150545748 | |||||||
chr5:150545991 | C | CT | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(126): Show |
146 | HG00323.hp2 HG00438.hp1 HG00621.hp2 others(143): Show |
intron_variant | MODIFIER | c.2145+529dupT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 150545991 | ||||||
chr5:150545991 | C | CTT | 12 | a0001c0001t0001g0262 a0001c0001t0007g0134 a0001c0001t0011g0241 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2145+528_2145+529d others(4): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 150545991 | ||||||
chr5:150545991 | CT | C | 58 | a0001c0001t0002g0041 a0001c0001t0002g0171 a0001c0001t0052g0041 others(55): Show |
72 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2145+529delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 150545991 | ||||||
chr5:150545991 | CTT | C | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2145+528_2145+529d others(4): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr5 | 150545991 | ||||||
chr5:150546037 | G | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(91): Show |
106 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.2145+551G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546037 | |||||||
chr5:150546046 | G | A | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2145+560G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546046 | |||||||
chr5:150546061 | G | A | 1 | a0001c0006t0009g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2145+575G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546061 | |||||||
chr5:150546145 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2145+659G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546145 | |||||||
chr5:150546247 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(132): Show |
154 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.2145+761C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546247 | |||||||
chr5:150546255 | C | G | 1 | a0002c0012t0010g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2145+769C>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546255 | |||||||
chr5:150546312 | T | G | 29 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(26): Show |
33 | HG00323.hp2 HG00673.hp2 HG02074.hp2 others(30): Show |
intron_variant | MODIFIER | c.2145+826T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546312 | |||||||
chr5:150546472 | C | T | 5 | a0001c0001t0069g0311 a0001c0006t0009g0003 a0001c0006t0009g0016 others(2): Show |
9 | HG01884.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2145+986C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546472 | |||||||
chr5:150546488 | C | T | 2 | a0001c0004t0002g0200 a0001c0004t0006g0195 |
2 | HG00558.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2145+1002C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546488 | |||||||
chr5:150546561 | G | T | 1 | a0001c0002t0004g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2145+1075G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546561 | |||||||
chr5:150546674 | C | T | 1 | a0001c0001t0050g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2145+1188C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546674 | |||||||
chr5:150546717 | G | T | 27 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(24): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
intron_variant | MODIFIER | c.2145+1231G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546717 | |||||||
chr5:150546973 | T | A | 1 | a0001c0016t0083g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2146-1245T>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150546973 | |||||||
chr5:150547004 | C | T | 1 | a0001c0001t0032g0334 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2146-1214C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547004 | |||||||
chr5:150547044 | C | T | 1 | a0001c0001t0070g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2146-1174C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547044 | |||||||
chr5:150547108 | G | T | 1 | a0001c0002t0018g0088 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2146-1110G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547108 | |||||||
chr5:150547151 | A | C | 2 | a0001c0004t0029g0169 a0001c0004t0029g0228 |
2 | HG00099.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.2146-1067A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547151 | |||||||
chr5:150547398 | G | T | 1 | a0001c0003t0005g0060 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2146-820G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547398 | |||||||
chr5:150547411 | G | T | 2 | a0001c0011t0058g0153 a0001c0011t0064g0158 |
2 | HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2146-807G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547411 | |||||||
chr5:150547436 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(193): Show |
223 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2146-782T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547436 | |||||||
chr5:150547437 | G | A | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2146-781G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547437 | |||||||
chr5:150547612 | T | C | 3 | a0001c0001t0024g0218 a0001c0001t0041g0292 a0001c0014t0040g0299 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2146-606T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547612 | |||||||
chr5:150547703 | A | C | 7 | a0001c0001t0011g0221 a0001c0001t0011g0229 a0001c0001t0011g0241 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2146-515A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547703 | |||||||
chr5:150547738 | T | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2146-480T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547738 | |||||||
chr5:150547742 | G | A | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2146-476G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547742 | |||||||
chr5:150547780 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(193): Show |
223 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2146-438A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150547780 | |||||||
chr5:150548020 | A | G | 1 | a0001c0001t0021g0073 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2146-198A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150548020 | |||||||
chr5:150548053 | G | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0326 |
2 | HG02015.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.2146-165G>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 11/14 | chr5 | 150548053 | |||||||
chr5:150548621 | C | T | 41 | a0001c0001t0002g0162 a0001c0003t0005g0004 a0001c0003t0005g0019 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2316+233C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150548621 | |||||||
chr5:150548630 | G | A | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2316+242G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150548630 | |||||||
chr5:150548782 | T | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(192): Show |
222 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.2316+394T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150548782 | |||||||
chr5:150548845 | A | G | 2 | a0001c0001t0002g0041 a0001c0001t0052g0041 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2316+457A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150548845 | |||||||
chr5:150549034 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0052g0041 |
2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2317-644C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549034 | |||||||
chr5:150549104 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0307 |
2 | HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.2317-574C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549104 | |||||||
chr5:150549297 | C | T | 1 | a0001c0001t0044g0114 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2317-381C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549297 | |||||||
chr5:150549516 | C | A | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2317-162C>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549516 | |||||||
chr5:150549613 | G | A | 1 | a0001c0007t0039g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2317-65G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549613 | |||||||
chr5:150549661 | C | T | 1 | a0001c0002t0003g0111 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2317-17C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 12/14 | chr5 | 150549661 | |||||||
chr5:150549879 | AAGTT | A | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2426+99_2426+102de others(5): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 150549879 | ||||||
chr5:150549929 | A | C | 1 | a0001c0005t0002g0170 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2426+142A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150549929 | |||||||
chr5:150550098 | G | A | 1 | a0001c0001t0004g0168 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2426+311G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550098 | |||||||
chr5:150550105 | CT | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(184): Show |
211 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(208): Show |
intron_variant | MODIFIER | c.2426+334delT | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 150550105 | ||||||
chr5:150550204 | G | C | 1 | a0001c0001t0081g0069 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2426+417G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550204 | |||||||
chr5:150550225 | C | T | 1 | a0001c0001t0026g0040 | 2 | HG00673.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.2426+438C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550225 | |||||||
chr5:150550276 | A | T | 7 | a0001c0001t0011g0221 a0001c0001t0011g0229 a0001c0001t0011g0241 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2426+489A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550276 | |||||||
chr5:150550294 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2426+507G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550294 | |||||||
chr5:150550453 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0007g0131 a0001c0001t0007g0135 others(2): Show |
6 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2426+666G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550453 | |||||||
chr5:150550480 | C | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0036 others(132): Show |
154 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.2426+693C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550480 | |||||||
chr5:150550491 | C | T | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2426+704C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550491 | |||||||
chr5:150550622 | A | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0325 |
2 | NA19007.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2426+835A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550622 | |||||||
chr5:150550809 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2427-944A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550809 | |||||||
chr5:150550950 | C | T | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2427-803C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550950 | |||||||
chr5:150550970 | GTCA | G | 40 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(37): Show |
44 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.2427-770_2427-768d others(5): Show |
NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 150550970 | ||||||
chr5:150550996 | C | T | 14 | a0001c0001t0008g0014 a0001c0001t0008g0265 a0001c0001t0008g0266 others(11): Show |
17 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2427-757C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150550996 | |||||||
chr5:150551384 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2427-369G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551384 | |||||||
chr5:150551396 | TA | T | 7 | a0001c0001t0001g0256 a0001c0001t0002g0226 a0001c0001t0006g0164 others(4): Show |
7 | HG00323.hp2 HG02895.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.2427-345delA | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr5 | 150551396 | ||||||
chr5:150551397 | A | T | 1 | a0001c0006t0079g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2427-356A>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551397 | |||||||
chr5:150551409 | G | C | 1 | a0001c0001t0004g0119 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2427-344G>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551409 | |||||||
chr5:150551451 | A | G | 1 | a0001c0019t0075g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2427-302A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551451 | |||||||
chr5:150551494 | C | T | 13 | a0001c0001t0019g0219 a0001c0001t0019g0305 a0001c0001t0019g0330 others(10): Show |
13 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2427-259C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551494 | |||||||
chr5:150551571 | G | A | 2 | a0001c0003t0005g0058 a0001c0003t0005g0061 |
2 | NA18943.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2427-182G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551571 | |||||||
chr5:150551588 | A | G | 1 | a0001c0003t0005g0059 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2427-165A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551588 | |||||||
chr5:150551660 | T | G | 263 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(260): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.2427-93T>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 13/14 | chr5 | 150551660 | |||||||
chr5:150552231 | A | C | 41 | a0001c0003t0005g0004 a0001c0003t0005g0019 a0001c0003t0005g0022 others(38): Show |
45 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.2529+376A>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552231 | |||||||
chr5:150552294 | C | T | 1 | a0001c0007t0039g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2529+439C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552294 | |||||||
chr5:150552351 | T | C | 1 | a0001c0002t0003g0098 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2529+496T>C | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552351 | |||||||
chr5:150552436 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0260 |
2 | HG02040.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.2529+581G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552436 | |||||||
chr5:150552519 | G | A | 4 | a0001c0001t0021g0071 a0001c0001t0021g0072 a0001c0001t0021g0073 others(1): Show |
4 | NA18974.hp1 NA19063.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2529+664G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552519 | |||||||
chr5:150552642 | C | T | 27 | a0001c0001t0004g0011 a0001c0001t0004g0028 a0001c0001t0004g0033 others(24): Show |
31 | HG00438.hp2 HG02056.hp1 HG02717.hp1 others(28): Show |
intron_variant | MODIFIER | c.2530-571C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552642 | |||||||
chr5:150552868 | C | T | 1 | a0001c0001t0024g0296 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2530-345C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552868 | |||||||
chr5:150552908 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2530-305G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552908 | |||||||
chr5:150552940 | G | A | 1 | a0001c0013t0047g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2530-273G>A | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150552940 | |||||||
chr5:150553040 | C | T | 166 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(163): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.2530-173C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150553040 | |||||||
chr5:150553102 | A | G | 1 | a0001c0001t0016g0034 | 2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2530-111A>G | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150553102 | |||||||
chr5:150553149 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2530-64C>T | NDST1 | ENSG00000070614.15 | transcript | ENST00000261797.7 | protein_coding | 14/14 | chr5 | 150553149 |