Item | Value |
---|---|
geneid | 54801 |
ensemblid | ENSG00000147874.11 |
hgncid | 25948 |
symbol | HAUS6 |
name | HAUS augmin like complex subunit 6 |
refseq_nuc | NM_017645.5 |
refseq_prot | NP_060115.3 |
ensembl_nuc | ENST00000380502.8 |
ensembl_prot | ENSP00000369871.3 |
mane_status | MANE Select |
chr | chr9 |
start | 19053141 |
end | 19102904 |
strand | - |
ver | v1.2 |
region | chr9:19053141-19102904 |
region5000 | chr9:19048141-19107904 |
regionname0 | HAUS6_chr9_19053141_19102904 |
regionname5000 | HAUS6_chr9_19048141_19107904 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 955 | 298 | 64 | 48 | 142 | 10 | 33 | 114 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0002 | 0/0 | 955 | 39 | 7 | 7 | 22 | 1 | 2 | 16 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0003 | 0/0 | 955 | 23 | 4 | 7 | 4 | 3 | 5 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0004 | 0/1 | 955 | 9 | 1 | 2 | 0 | 2 | 3 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0005 | 0/0 | 955 | 8 | 0 | 0 | 6 | 0 | 2 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0006 | 0/0 | 955 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0007 | 0/0 | 955 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0008 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0009 | 0/0 | 955 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0010 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0011 | 0/0 | 955 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0012 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MGSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0013 | 0/0 | 955 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0014 | 0/0 | 941 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(936): Show |
chr9 | 19048141 | 19107904 |
a0015 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0016 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0017 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0018 | 0/0 | 955 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0019 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0020 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0021 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0022 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | MSSAS others(950): Show |
chr9 | 19048141 | 19107904 |
a0023 | 0/0 | 955 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | MGSAS others(950): Show |
chr9 | 19048141 | 19107904 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2865 | 110 | 11 | 24 | 50 | 5 | 20 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0002 | 1/0 | 2865 | 93 | 7 | 15 | 61 | 3 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0004 | 0/0 | 2865 | 31 | 17 | 5 | 7 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0005 | 0/0 | 2865 | 27 | 17 | 1 | 3 | 0 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0007 | 0/0 | 2865 | 15 | 0 | 2 | 13 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0010 | 0/0 | 2865 | 4 | 0 | 0 | 4 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0011 | 0/0 | 2865 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0012 | 0/0 | 2865 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0019 | 0/0 | 2865 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0020 | 0/0 | 2865 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0024 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0026 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0029 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0031 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0035 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0001c0037 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0002c0003 | 0/0 | 2865 | 38 | 7 | 7 | 21 | 1 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0002c0030 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0003c0006 | 0/0 | 2865 | 23 | 4 | 7 | 4 | 3 | 5 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0004c0008 | 0/1 | 2865 | 9 | 1 | 2 | 0 | 2 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0005c0009 | 0/0 | 2865 | 6 | 0 | 0 | 6 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0005c0023 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0005c0036 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0006c0014 | 0/0 | 2865 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0006c0016 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0007c0013 | 0/0 | 2865 | 4 | 3 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0008c0017 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0009c0015 | 0/0 | 2865 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0010c0021 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0011c0018 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0012c0042 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGGG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0013c0038 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0014c0033 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0015c0032 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0016c0034 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0017c0039 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0018c0022 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0019c0040 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0020c0028 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0021c0027 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0022c0025 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGAG others(2860): Show |
chr9 | 19048141 | 19107904 | ||
a0023c0041 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | ATGGG others(2860): Show |
chr9 | 19048141 | 19107904 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6323 | 106 | 10 | 24 | 48 | 5 | 19 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0001t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0001t0015 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0001t0020 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0001t0029 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0002t0002 | 1/0 | 6323 | 88 | 6 | 15 | 57 | 3 | 6 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0002t0012 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0002t0017 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0002t0018 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0002t0031 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0004t0003 | 0/0 | 6324 | 31 | 17 | 5 | 7 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0001c0005t0003 | 0/0 | 6324 | 2 | 1 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0001c0005t0004 | 0/0 | 6323 | 20 | 12 | 1 | 3 | 0 | 4 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0005t0008 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0005t0023 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0007t0002 | 0/0 | 6323 | 14 | 0 | 2 | 12 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0007t0024 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0001c0010t0002 | 0/0 | 6323 | 4 | 0 | 0 | 4 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0011t0004 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0012t0004 | 0/0 | 6323 | 4 | 4 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0019t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0019t0015 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0020t0001 | 0/0 | 6323 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0024t0021 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0026t0028 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0029t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0031t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0035t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0001c0037t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0002c0003t0005 | 0/0 | 6323 | 27 | 0 | 5 | 20 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0002c0003t0007 | 0/0 | 6324 | 7 | 7 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0002c0003t0009 | 0/0 | 6323 | 3 | 0 | 2 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0002c0003t0032 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0002c0030t0005 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0003c0006t0003 | 0/0 | 6324 | 22 | 4 | 7 | 3 | 3 | 5 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0003c0006t0027 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0004c0008t0006 | 0/1 | 6323 | 8 | 1 | 2 | 0 | 2 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0004c0008t0030 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0005c0009t0001 | 0/0 | 6323 | 5 | 0 | 0 | 5 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0005c0009t0019 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0005c0023t0001 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0005c0036t0002 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0006c0014t0010 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0006c0014t0022 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0006c0014t0025 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0006c0016t0014 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0007c0013t0003 | 0/0 | 6324 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0007c0013t0011 | 0/0 | 6324 | 3 | 3 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0008c0017t0013 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0009c0015t0003 | 0/0 | 6324 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0010c0021t0003 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0011c0018t0010 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0012c0042t0016 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0013c0038t0003 | 0/0 | 6324 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0014c0033t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0015c0032t0001 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0016c0034t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0017c0039t0003 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0018c0022t0026 | 0/0 | 6324 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6319): Show |
chr9 | 19048141 | 19107904 |
a0019c0040t0004 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0020c0028t0005 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0021c0027t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0022c0025t0002 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
a0023c0041t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | CTTAA others(6318): Show |
chr9 | 19048141 | 19107904 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0015g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0020g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0001t0029g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0001 | 1/0 | 6 | 0 | 3 | 1 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0012g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0018g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0002t0031g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0004t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0005t0023g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0007t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0010t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0011t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0012t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0019t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0019t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0020t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0024t0021g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0026t0028g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0029t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0031t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0035t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0001c0037t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0009g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0003t0032g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0002c0030t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0003c0006t0027g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0025 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0006g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0004c0008t0030g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0009t0019g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0023t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0005c0036t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0014t0025g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0016t0014g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0006c0016t0014g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0007c0013t0011g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0008c0017t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0008c0017t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0009c0015t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0009c0015t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0010c0021t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0010c0021t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0011c0018t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0011c0018t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0012c0042t0016g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0013c0038t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0014c0033t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0015c0032t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0016c0034t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0017c0039t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0018c0022t0026g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0019c0040t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0020c0028t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0021c0027t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0022c0025t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
a0023c0041t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00099 | hp2 | a0004 | c0008 | t0006 | g0025 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00140 | hp1 | a0003 | c0006 | t0003 | g0161 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00140 | hp2 | a0002 | c0003 | t0009 | g0313 | EUR | GBR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | FIN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00408 | hp1 | a0005 | c0009 | t0001 | g0208 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00408 | hp2 | a0001 | c0031 | t0002 | g0209 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00423 | hp2 | a0001 | c0007 | t0002 | g0168 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00438 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00438 | hp2 | a0005 | c0009 | t0001 | g0239 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00544 | hp2 | a0001 | c0007 | t0002 | g0142 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00558 | hp1 | a0001 | c0007 | t0002 | g0152 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00609 | hp2 | a0001 | c0004 | t0003 | g0289 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00621 | hp2 | a0001 | c0002 | t0012 | g0075 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00639 | hp2 | a0002 | c0003 | t0005 | g0358 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00642 | hp2 | a0003 | c0006 | t0003 | g0154 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | CHS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00733 | hp1 | a0003 | c0006 | t0003 | g0135 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00733 | hp2 | a0002 | c0003 | t0005 | g0355 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00735 | hp2 | a0002 | c0003 | t0009 | g0315 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG00741 | hp2 | a0002 | c0003 | t0005 | g0331 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01069 | hp1 | a0001 | c0020 | t0001 | g0018 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01070 | hp2 | a0004 | c0008 | t0006 | g0366 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01074 | hp2 | a0004 | c0008 | t0006 | g0362 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01081 | hp1 | a0001 | c0005 | t0004 | g0132 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01081 | hp2 | a0003 | c0006 | t0003 | g0013 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01106 | hp1 | a0003 | c0006 | t0003 | g0166 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01109 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01167 | hp2 | a0002 | c0003 | t0005 | g0341 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01169 | hp2 | a0002 | c0003 | t0005 | g0347 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01192 | hp1 | a0002 | c0003 | t0009 | g0314 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01192 | hp2 | a0001 | c0004 | t0003 | g0301 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01243 | hp2 | a0007 | c0013 | t0003 | g0294 | AMR | PUR | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0059 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01257 | hp2 | a0001 | c0004 | t0003 | g0023 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01258 | hp1 | a0001 | c0004 | t0003 | g0023 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01433 | hp1 | a0001 | c0004 | t0003 | g0302 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01516 | hp1 | a0001 | c0004 | t0003 | g0022 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01517 | hp1 | a0001 | c0004 | t0003 | g0022 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0011 | EUR | IBS | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01884 | hp2 | a0001 | c0005 | t0004 | g0012 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01891 | hp1 | a0001 | c0004 | t0003 | g0106 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01891 | hp2 | a0012 | c0042 | t0016 | g0318 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01928 | hp2 | a0001 | c0007 | t0002 | g0143 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01934 | hp2 | a0001 | c0007 | t0002 | g0144 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01943 | hp1 | a0013 | c0038 | t0003 | g0292 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01981 | hp2 | a0003 | c0006 | t0003 | g0148 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02015 | hp2 | a0002 | c0003 | t0032 | g0353 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02040 | hp2 | a0002 | c0003 | t0005 | g0346 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02055 | hp1 | a0001 | c0011 | t0004 | g0131 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02055 | hp2 | a0008 | c0017 | t0013 | g0172 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02056 | hp1 | a0002 | c0003 | t0005 | g0359 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02129 | hp2 | a0001 | c0002 | t0031 | g0325 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02132 | hp1 | a0003 | c0006 | t0027 | g0164 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02135 | hp1 | a0001 | c0004 | t0003 | g0290 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02145 | hp1 | a0003 | c0006 | t0003 | g0150 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02145 | hp2 | a0006 | c0014 | t0022 | g0124 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02155 | hp1 | a0002 | c0003 | t0005 | g0344 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02155 | hp2 | a0009 | c0015 | t0003 | g0285 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02165 | hp1 | a0002 | c0003 | t0005 | g0007 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CDX | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02257 | hp1 | a0001 | c0004 | t0003 | g0310 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02258 | hp1 | a0001 | c0026 | t0028 | g0170 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02258 | hp2 | a0001 | c0004 | t0003 | g0298 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02280 | hp1 | a0001 | c0011 | t0004 | g0129 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02280 | hp2 | a0001 | c0005 | t0004 | g0012 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02293 | hp2 | a0003 | c0006 | t0003 | g0155 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02451 | hp1 | a0001 | c0004 | t0003 | g0306 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02451 | hp2 | a0003 | c0006 | t0003 | g0014 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02523 | hp1 | a0014 | c0033 | t0001 | g0226 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | KHV | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0303 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02572 | hp2 | a0001 | c0005 | t0008 | g0328 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02602 | hp1 | a0001 | c0005 | t0004 | g0098 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02615 | hp2 | a0001 | c0004 | t0003 | g0309 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02622 | hp1 | a0001 | c0011 | t0004 | g0130 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02622 | hp2 | a0001 | c0004 | t0003 | g0295 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02630 | hp1 | a0001 | c0012 | t0004 | g0101 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02630 | hp2 | a0001 | c0005 | t0004 | g0115 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0304 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02647 | hp2 | a0001 | c0012 | t0004 | g0099 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02683 | hp1 | a0001 | c0005 | t0004 | g0121 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02683 | hp2 | a0001 | c0020 | t0001 | g0018 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02698 | hp1 | a0015 | c0032 | t0001 | g0224 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02717 | hp2 | a0010 | c0021 | t0003 | g0307 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02735 | hp1 | a0002 | c0003 | t0005 | g0330 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02738 | hp1 | a0001 | c0001 | t0029 | g0319 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02809 | hp1 | a0001 | c0002 | t0018 | g0171 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02809 | hp2 | a0001 | c0005 | t0003 | g0297 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02818 | hp1 | a0002 | c0003 | t0007 | g0368 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02818 | hp2 | a0001 | c0005 | t0004 | g0117 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02895 | hp2 | a0007 | c0013 | t0011 | g0324 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02896 | hp2 | a0007 | c0013 | t0011 | g0323 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02897 | hp2 | a0007 | c0013 | t0011 | g0322 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02922 | hp1 | a0006 | c0014 | t0025 | g0126 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02965 | hp1 | a0001 | c0005 | t0004 | g0109 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02965 | hp2 | a0002 | c0003 | t0007 | g0335 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02970 | hp1 | a0001 | c0005 | t0008 | g0326 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02970 | hp2 | a0006 | c0016 | t0014 | g0123 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03017 | hp2 | a0001 | c0005 | t0023 | g0095 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03041 | hp1 | a0002 | c0003 | t0007 | g0334 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03041 | hp2 | a0016 | c0034 | t0001 | g0201 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03098 | hp1 | a0001 | c0004 | t0003 | g0283 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03098 | hp2 | a0001 | c0019 | t0015 | g0119 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03130 | hp1 | a0001 | c0005 | t0004 | g0133 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03130 | hp2 | a0002 | c0003 | t0007 | g0337 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03139 | hp2 | a0001 | c0011 | t0004 | g0128 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03195 | hp1 | a0001 | c0037 | t0001 | g0311 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03195 | hp2 | a0001 | c0012 | t0004 | g0100 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03209 | hp1 | a0002 | c0003 | t0007 | g0333 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03209 | hp2 | a0001 | c0004 | t0003 | g0282 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03225 | hp1 | a0001 | c0005 | t0004 | g0118 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03225 | hp2 | a0001 | c0004 | t0003 | g0300 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03453 | hp1 | a0011 | c0018 | t0010 | g0102 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0215 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0116 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03486 | hp2 | a0008 | c0017 | t0013 | g0173 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03490 | hp1 | a0001 | c0005 | t0003 | g0114 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03491 | hp2 | a0001 | c0005 | t0004 | g0122 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03516 | hp1 | a0001 | c0005 | t0008 | g0329 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03516 | hp2 | a0001 | c0004 | t0003 | g0305 | AFR | ESN | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03540 | hp1 | a0011 | c0018 | t0010 | g0103 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03540 | hp2 | a0003 | c0006 | t0003 | g0151 | AFR | GWD | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03579 | hp1 | a0001 | c0012 | t0004 | g0127 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03654 | hp2 | a0001 | c0005 | t0004 | g0113 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03669 | hp1 | a0004 | c0008 | t0006 | g0363 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03688 | hp1 | a0003 | c0006 | t0003 | g0147 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03688 | hp2 | a0003 | c0006 | t0003 | g0167 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03704 | hp1 | a0004 | c0008 | t0006 | g0365 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03710 | hp1 | a0002 | c0003 | t0005 | g0007 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03831 | hp1 | a0005 | c0023 | t0001 | g0136 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03834 | hp1 | a0003 | c0006 | t0003 | g0165 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03942 | hp1 | a0004 | c0008 | t0030 | g0320 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04115 | hp2 | a0003 | c0006 | t0003 | g0158 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04184 | hp1 | a0018 | c0022 | t0026 | g0169 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04184 | hp2 | a0005 | c0036 | t0002 | g0069 | SAS | BEB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0074 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04228 | hp1 | a0003 | c0006 | t0003 | g0183 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG04228 | hp2 | a0009 | c0015 | t0003 | g0284 | SAS | STU | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0108 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18522 | hp2 | a0003 | c0006 | t0003 | g0160 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18612 | hp2 | a0002 | c0003 | t0005 | g0352 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18747 | hp1 | a0005 | c0009 | t0001 | g0228 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CHB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0111 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18939 | hp2 | a0001 | c0004 | t0003 | g0105 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18942 | hp1 | a0001 | c0007 | t0002 | g0156 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18945 | hp1 | a0002 | c0003 | t0005 | g0343 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18945 | hp2 | a0002 | c0003 | t0005 | g0342 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18947 | hp1 | a0002 | c0003 | t0005 | g0345 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18947 | hp2 | a0005 | c0009 | t0001 | g0238 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18953 | hp2 | a0002 | c0003 | t0005 | g0354 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18954 | hp2 | a0005 | c0009 | t0019 | g0202 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18957 | hp1 | a0001 | c0007 | t0002 | g0159 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0104 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18961 | hp2 | a0001 | c0007 | t0002 | g0145 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18963 | hp2 | a0001 | c0004 | t0003 | g0288 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18964 | hp2 | a0001 | c0007 | t0002 | g0137 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18967 | hp1 | a0001 | c0007 | t0002 | g0163 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18971 | hp2 | a0001 | c0007 | t0002 | g0140 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18977 | hp2 | a0001 | c0029 | t0001 | g0227 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18979 | hp2 | a0001 | c0007 | t0002 | g0139 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18980 | hp2 | a0001 | c0035 | t0001 | g0240 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18981 | hp2 | a0001 | c0010 | t0002 | g0008 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0287 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18983 | hp2 | a0002 | c0003 | t0005 | g0007 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18985 | hp2 | a0001 | c0002 | t0012 | g0031 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18987 | hp1 | a0003 | c0006 | t0003 | g0138 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18987 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18990 | hp1 | a0019 | c0040 | t0004 | g0316 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18991 | hp1 | a0001 | c0007 | t0002 | g0153 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18993 | hp2 | a0001 | c0005 | t0004 | g0120 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18994 | hp1 | a0002 | c0003 | t0005 | g0356 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18999 | hp1 | a0002 | c0003 | t0005 | g0361 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19002 | hp2 | a0002 | c0003 | t0005 | g0351 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19004 | hp1 | a0001 | c0002 | t0017 | g0051 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19009 | hp1 | a0001 | c0005 | t0004 | g0107 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19010 | hp1 | a0001 | c0010 | t0002 | g0042 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19010 | hp2 | a0001 | c0007 | t0002 | g0141 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19012 | hp1 | a0002 | c0003 | t0005 | g0349 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19030 | hp1 | a0001 | c0005 | t0008 | g0327 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19030 | hp2 | a0002 | c0003 | t0007 | g0338 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19043 | hp1 | a0001 | c0004 | t0003 | g0024 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19043 | hp2 | a0001 | c0004 | t0003 | g0281 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19062 | hp1 | a0002 | c0003 | t0005 | g0348 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19062 | hp2 | a0001 | c0004 | t0003 | g0291 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19063 | hp1 | a0002 | c0003 | t0005 | g0339 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19066 | hp1 | a0020 | c0028 | t0005 | g0340 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19066 | hp2 | a0021 | c0027 | t0002 | g0071 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19068 | hp1 | a0003 | c0006 | t0003 | g0157 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19070 | hp1 | a0002 | c0030 | t0005 | g0321 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19072 | hp2 | a0002 | c0003 | t0005 | g0360 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19074 | hp1 | a0022 | c0025 | t0002 | g0056 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19079 | hp1 | a0002 | c0003 | t0005 | g0350 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19080 | hp1 | a0001 | c0005 | t0004 | g0134 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19081 | hp2 | a0005 | c0009 | t0001 | g0237 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19083 | hp1 | a0001 | c0019 | t0001 | g0029 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19083 | hp2 | a0002 | c0003 | t0005 | g0357 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19086 | hp1 | a0001 | c0010 | t0002 | g0040 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19086 | hp2 | a0001 | c0001 | t0020 | g0241 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19087 | hp1 | a0001 | c0007 | t0024 | g0162 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19088 | hp1 | a0003 | c0006 | t0003 | g0014 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19089 | hp1 | a0002 | c0003 | t0005 | g0332 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19091 | hp1 | a0001 | c0010 | t0002 | g0008 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0182 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA19240 | hp2 | a0001 | c0004 | t0003 | g0299 | AFR | YRI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20129 | hp1 | a0002 | c0003 | t0007 | g0336 | AFR | ASW | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20129 | hp2 | a0001 | c0004 | t0003 | g0024 | AFR | ASW | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20752 | hp2 | a0003 | c0006 | t0003 | g0146 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20805 | hp1 | a0003 | c0006 | t0003 | g0013 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20805 | hp2 | a0004 | c0008 | t0006 | g0364 | EUR | TSI | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01123 | hp1 | a0003 | c0006 | t0003 | g0149 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG01123 | hp2 | a0001 | c0004 | t0003 | g0286 | AMR | CLM | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02109 | hp1 | a0001 | c0005 | t0004 | g0110 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02109 | hp2 | a0006 | c0016 | t0014 | g0125 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02486 | hp1 | a0001 | c0005 | t0004 | g0112 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG02486 | hp2 | a0004 | c0008 | t0006 | g0367 | AFR | ACB | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03471 | hp1 | a0001 | c0004 | t0003 | g0296 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG03471 | hp2 | a0017 | c0039 | t0003 | g0308 | AFR | MSL | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0067 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
HG06807 | hp2 | a0006 | c0014 | t0010 | g0277 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA20300 | hp2 | a0010 | c0021 | t0003 | g0293 | AFR | USA | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA21309 | hp1 | a0001 | c0024 | t0021 | g0177 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
NA21309 | hp2 | a0023 | c0041 | t0001 | g0317 | AFR | LWK | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
homoSapiens | chm13v2 | a0004 | c0008 | t0006 | g0025 | REF | REF | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0001 | REF | REF | HAUS6_chr9_19048141_19107904 | HAUS6 | chr9 | 19048141 | 19107904 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056387 | T | A | 1 | a0014 | 1 | HG02523.hp1 | stop_gained | HIGH | c.2824A>T | p.Lys942* | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3077/6323 | 2824/2868 | 942/955 | chr9 | 19056387 | |||
chr9:19057967 | A | T | 1 | a0022 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.2800T>A | p.Leu934Ile | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 3053/6323 | 2800/2868 | 934/955 | chr9 | 19057967 | |||
chr9:19057987 | C | T | 1 | a0015 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.2780G>A | p.Ser927Asn | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 3033/6323 | 2780/2868 | 927/955 | chr9 | 19057987 | |||
chr9:19058050 | G | A | 1 | a0016 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2717C>T | p.Ser906Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2970/6323 | 2717/2868 | 906/955 | chr9 | 19058050 | |||
chr9:19058057 | T | G | 1 | a0021 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2710A>C | p.Lys904Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2963/6323 | 2710/2868 | 904/955 | chr9 | 19058057 | |||
chr9:19058431 | G | C | 1 | a0008 | 2 | HG02055.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.2336C>G | p.Thr779Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2589/6323 | 2336/2868 | 779/955 | chr9 | 19058431 | |||
chr9:19058485 | C | A | 1 | a0003 | 23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
missense_variant | MODERATE | c.2282G>T | p.Ser761Ile | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2535/6323 | 2282/2868 | 761/955 | chr9 | 19058485 | |||
chr9:19058571 | A | T | 1 | a0018 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.2196T>A | p.Phe732Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2449/6323 | 2196/2868 | 732/955 | chr9 | 19058571 | |||
chr9:19058735 | G | A | 1 | a0011 | 2 | HG03453.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.2032C>T | p.Pro678Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2285/6323 | 2032/2868 | 678/955 | chr9 | 19058735 | |||
chr9:19058745 | G | C | 2 | a0002 a0020 |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
missense_variant | MODERATE | c.2022C>G | p.His674Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2275/6323 | 2022/2868 | 674/955 | chr9 | 19058745 | |||
chr9:19058923 | G | A | 3 | a0003 a0006 a0011 |
30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
missense_variant | MODERATE | c.1844C>T | p.Ala615Val | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2097/6323 | 1844/2868 | 615/955 | chr9 | 19058923 | |||
chr9:19060106 | G | A | 1 | a0021 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.1747C>T | p.Arg583Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/17 | 2000/6323 | 1747/2868 | 583/955 | chr9 | 19060106 | |||
chr9:19060199 | A | T | 1 | a0004 | 8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
missense_variant | MODERATE | c.1654T>A | p.Ser552Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/17 | 1907/6323 | 1654/2868 | 552/955 | chr9 | 19060199 | |||
chr9:19063097 | T | G | 1 | a0020 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.1540A>C | p.Lys514Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/17 | 1793/6323 | 1540/2868 | 514/955 | chr9 | 19063097 | |||
chr9:19078259 | C | A | 1 | a0007 | 4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.1108G>T | p.Val370Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1361/6323 | 1108/2868 | 370/955 | chr9 | 19078259 | |||
chr9:19078276 | G | C | 1 | a0013 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.1091C>G | p.Thr364Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1344/6323 | 1091/2868 | 364/955 | chr9 | 19078276 | |||
chr9:19080572 | T | C | 2 | a0010 a0017 |
3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
missense_variant | MODERATE | c.971A>G | p.Gln324Arg | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1224/6323 | 971/2868 | 324/955 | chr9 | 19080572 | |||
chr9:19080579 | G | A | 1 | a0005 | 8 | HG00408.hp1 HG00438.hp2 HG03831.hp1 others(5): Show |
missense_variant | MODERATE | c.964C>T | p.Arg322Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1217/6323 | 964/2868 | 322/955 | chr9 | 19080579 | |||
chr9:19086739 | G | C | 1 | a0017 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.694C>G | p.Gln232Glu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/17 | 947/6323 | 694/2868 | 232/955 | chr9 | 19086739 | |||
chr9:19089419 | T | C | 1 | a0012 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.577A>G | p.Asn193Asp | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/17 | 830/6323 | 577/2868 | 193/955 | chr9 | 19089419 | |||
chr9:19093270 | C | T | 1 | a0008 | 2 | HG02055.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.337G>A | p.Gly113Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 590/6323 | 337/2868 | 113/955 | chr9 | 19093270 | |||
chr9:19093290 | C | G | 1 | a0009 | 2 | HG02155.hp2 HG04228.hp2 |
missense_variant | MODERATE | c.317G>C | p.Ser106Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 570/6323 | 317/2868 | 106/955 | chr9 | 19093290 | |||
chr9:19102615 | G | A | 1 | a0019 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.37C>T | p.His13Tyr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 290/6323 | 37/2868 | 13/955 | chr9 | 19102615 | |||
chr9:19102648 | T | C | 2 | a0012 a0023 |
2 | HG01891.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.4A>G | p.Ser2Gly | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 257/6323 | 4/2868 | 2/955 | chr9 | 19102648 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056376 | A | G | 1 | a0001c0026 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.2835T>C | p.Asp945Asp | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3088/6323 | 2835/2868 | 945/955 | chr9 | 19056376 | |||
chr9:19058115 | G | A | 1 | a0011c0018 | 2 | HG03453.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.2652C>T | p.Thr884Thr | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2905/6323 | 2652/2868 | 884/955 | chr9 | 19058115 | |||
chr9:19058427 | G | A | 16 | a0001c0004 a0001c0005 a0001c0011 others(13): Show |
129 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(126): Show |
synonymous_variant | LOW | c.2340C>T | p.Leu780Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2593/6323 | 2340/2868 | 780/955 | chr9 | 19058427 | |||
chr9:19058708 | A | G | 1 | a0001c0024 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.2059T>C | p.Leu687Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2312/6323 | 2059/2868 | 687/955 | chr9 | 19058708 | |||
chr9:19058715 | T | G | 1 | a0001c0035 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.2052A>C | p.Ser684Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2305/6323 | 2052/2868 | 684/955 | chr9 | 19058715 | |||
chr9:19058781 | G | A | 1 | a0001c0010 | 4 | NA18981.hp2 NA19010.hp1 NA19086.hp1 others(1): Show |
synonymous_variant | LOW | c.1986C>T | p.Cys662Cys | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2239/6323 | 1986/2868 | 662/955 | chr9 | 19058781 | |||
chr9:19058823 | A | G | 3 | a0002c0003 a0002c0030 a0020c0028 |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
synonymous_variant | LOW | c.1944T>C | p.Phe648Phe | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/17 | 2197/6323 | 1944/2868 | 648/955 | chr9 | 19058823 | |||
chr9:19063110 | T | C | 12 | a0001c0001 a0001c0019 a0001c0020 others(9): Show |
128 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
synonymous_variant | LOW | c.1527A>G | p.Leu509Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/17 | 1780/6323 | 1527/2868 | 509/955 | chr9 | 19063110 | |||
chr9:19076669 | C | T | 1 | a0001c0029 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.1227G>A | p.Ser409Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/17 | 1480/6323 | 1227/2868 | 409/955 | chr9 | 19076669 | |||
chr9:19076675 | G | C | 13 | a0001c0001 a0001c0011 a0001c0020 others(10): Show |
131 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
synonymous_variant | LOW | c.1221C>G | p.Pro407Pro | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/17 | 1474/6323 | 1221/2868 | 407/955 | chr9 | 19076675 | |||
chr9:19078194 | T | G | 1 | a0001c0012 | 4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1173A>C | p.Leu391Leu | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/17 | 1426/6323 | 1173/2868 | 391/955 | chr9 | 19078194 | |||
chr9:19080601 | G | C | 1 | a0001c0020 | 2 | HG01069.hp1 HG02683.hp2 |
synonymous_variant | LOW | c.942C>G | p.Val314Val | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/17 | 1195/6323 | 942/2868 | 314/955 | chr9 | 19080601 | |||
chr9:19087156 | T | C | 8 | a0001c0004 a0001c0037 a0004c0008 others(5): Show |
50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
splice_region_variant&synonymous_variant | LOW | c.585A>G | p.Gln195Gln | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/17 | 838/6323 | 585/2868 | 195/955 | chr9 | 19087156 | |||
chr9:19093289 | A | G | 6 | a0001c0007 a0003c0006 a0005c0023 others(3): Show |
45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
synonymous_variant | LOW | c.318T>C | p.Ser106Ser | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/17 | 571/6323 | 318/2868 | 106/955 | chr9 | 19093289 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19053213 | A | G | 1 | a0001c0024t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3130T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3130 | chr9 | 19053213 | ||||||
chr9:19053249 | T | C | 11 | a0001c0005t0023 a0002c0003t0005 a0002c0003t0007 others(8): Show |
52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*3094A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3094 | chr9 | 19053249 | ||||||
chr9:19053281 | T | C | 2 | a0004c0008t0006 a0004c0008t0030 |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3062A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 3062 | chr9 | 19053281 | ||||||
chr9:19053349 | T | A | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2994A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2994 | chr9 | 19053349 | ||||||
chr9:19053377 | G | A | 1 | a0002c0003t0032 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2966C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2966 | chr9 | 19053377 | ||||||
chr9:19053420 | T | G | 1 | a0001c0005t0023 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2923A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2923 | chr9 | 19053420 | ||||||
chr9:19053489 | T | C | 1 | a0001c0002t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2854 | chr9 | 19053489 | ||||||
chr9:19053507 | A | C | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2836 | chr9 | 19053507 | ||||||
chr9:19053573 | A | G | 2 | a0004c0008t0006 a0004c0008t0030 |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2770T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2770 | chr9 | 19053573 | ||||||
chr9:19053581 | T | C | 2 | a0004c0008t0006 a0004c0008t0030 |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2762A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2762 | chr9 | 19053581 | ||||||
chr9:19053772 | C | A | 5 | a0001c0005t0004 a0001c0005t0008 a0001c0011t0004 others(2): Show |
33 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2571G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2571 | chr9 | 19053772 | ||||||
chr9:19053813 | A | G | 6 | a0002c0003t0005 a0002c0003t0007 a0002c0003t0009 others(3): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2530T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2530 | chr9 | 19053813 | ||||||
chr9:19053851 | G | C | 2 | a0004c0008t0006 a0004c0008t0030 |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2492C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2492 | chr9 | 19053851 | ||||||
chr9:19053919 | T | C | 26 | a0001c0004t0003 a0001c0005t0003 a0001c0005t0004 others(23): Show |
145 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*2424A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2424 | chr9 | 19053919 | ||||||
chr9:19053925 | T | C | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2418A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2418 | chr9 | 19053925 | ||||||
chr9:19054078 | A | C | 2 | a0006c0014t0010 a0011c0018t0010 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2265T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2265 | chr9 | 19054078 | ||||||
chr9:19054251 | C | T | 1 | a0006c0014t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2092G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2092 | chr9 | 19054251 | ||||||
chr9:19054340 | C | G | 1 | a0012c0042t0016 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 2003 | chr9 | 19054340 | ||||||
chr9:19054389 | C | T | 28 | a0001c0004t0003 a0001c0005t0003 a0001c0005t0004 others(25): Show |
148 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1954 | chr9 | 19054389 | ||||||
chr9:19054423 | C | A | 50 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0020 others(47): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*1920G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1920 | chr9 | 19054423 | ||||||
chr9:19054609 | G | T | 1 | a0001c0024t0021 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1734C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1734 | chr9 | 19054609 | ||||||
chr9:19054921 | G | C | 1 | a0005c0009t0019 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1422C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1422 | chr9 | 19054921 | ||||||
chr9:19054957 | A | T | 2 | a0006c0014t0010 a0011c0018t0010 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1386 | chr9 | 19054957 | ||||||
chr9:19055002 | A | AT | 1 | a0002c0003t0007 | 7 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1340dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1340 | chr9 | 19055002 | ||||||
chr9:19055068 | C | T | 1 | a0006c0016t0014 | 2 | HG02109.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1275G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1275 | chr9 | 19055068 | ||||||
chr9:19055071 | A | G | 1 | a0001c0002t0017 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1272 | chr9 | 19055071 | ||||||
chr9:19055092 | G | A | 1 | a0001c0001t0020 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1251C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1251 | chr9 | 19055092 | ||||||
chr9:19055142 | A | T | 2 | a0006c0016t0014 a0012c0042t0016 |
3 | HG01891.hp2 HG02109.hp2 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1201T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 1201 | chr9 | 19055142 | ||||||
chr9:19055528 | A | G | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*815T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 815 | chr9 | 19055528 | ||||||
chr9:19055967 | T | C | 36 | a0001c0001t0015 a0001c0004t0003 a0001c0005t0003 others(33): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*376A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 376 | chr9 | 19055967 | ||||||
chr9:19056100 | T | A | 1 | a0003c0006t0027 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*243A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 243 | chr9 | 19056100 | ||||||
chr9:19056149 | T | TA | 15 | a0001c0004t0003 a0001c0005t0003 a0001c0007t0024 others(12): Show |
72 | HG00140.hp1 HG00609.hp2 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*193dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 193 | chr9 | 19056149 | ||||||
chr9:19056160 | A | G | 1 | a0008c0017t0013 | 2 | HG02055.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*183T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 183 | chr9 | 19056160 | ||||||
chr9:19056210 | G | T | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 133 | chr9 | 19056210 | ||||||
chr9:19056279 | A | C | 1 | a0001c0002t0012 | 2 | HG00621.hp2 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*64T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 64 | chr9 | 19056279 | ||||||
chr9:19056325 | T | G | 1 | a0001c0026t0028 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 17/17 | 18 | chr9 | 19056325 | ||||||
chr9:19102779 | T | A | 2 | a0001c0001t0029 a0004c0008t0030 |
2 | HG02738.hp1 HG03942.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-128A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | chr9 | 19102779 | |||||||
chr9:19102830 | T | C | 9 | a0001c0002t0031 a0001c0005t0008 a0002c0003t0005 others(6): Show |
52 | HG00099.hp2 HG00639.hp2 HG00733.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-179A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/17 | 179 | chr9 | 19102830 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:19056484 | A | G | 1 | a0002c0003t0005g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2807-80T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056484 | |||||||
chr9:19056501 | T | C | 3 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0283 |
5 | HG01257.hp2 HG01258.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2807-97A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056501 | |||||||
chr9:19056508 | C | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2807-104G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056508 | |||||||
chr9:19056597 | CT | C | 8 | a0001c0005t0008g0328 a0002c0003t0007g0333 a0002c0003t0007g0334 others(5): Show |
8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2807-194delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056597 | |||||||
chr9:19056602 | T | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2807-198A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056602 | |||||||
chr9:19056726 | G | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0185 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.2807-322C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056726 | |||||||
chr9:19056750 | G | A | 2 | a0006c0016t0014g0123 a0006c0016t0014g0125 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2807-346C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056750 | |||||||
chr9:19056756 | G | A | 149 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(146): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.2807-352C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056756 | |||||||
chr9:19056794 | T | C | 1 | a0005c0009t0001g0228 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2807-390A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056794 | |||||||
chr9:19056858 | C | T | 22 | a0003c0006t0003g0013 a0003c0006t0003g0014 a0003c0006t0003g0135 others(19): Show |
24 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.2807-454G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056858 | |||||||
chr9:19056926 | T | TAA | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0273 |
3 | NA18973.hp1 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2807-524_2807-523d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19056926 | |||||||
chr9:19057007 | T | G | 1 | a0020c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2807-603A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057007 | |||||||
chr9:19057010 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2807-606A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057010 | |||||||
chr9:19057043 | CA | C | 4 | a0001c0012t0004g0099 a0001c0012t0004g0100 a0001c0012t0004g0101 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2807-640delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057043 | |||||||
chr9:19057085 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2807-681G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057085 | |||||||
chr9:19057156 | C | A | 2 | a0001c0004t0003g0024 a0001c0004t0003g0300 |
3 | HG03225.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2807-752G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057156 | |||||||
chr9:19057423 | G | A | 2 | a0001c0002t0002g0059 a0001c0002t0002g0064 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2806+538C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057423 | |||||||
chr9:19057553 | T | C | 143 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(140): Show |
151 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(148): Show |
intron_variant | MODIFIER | c.2806+408A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057553 | |||||||
chr9:19057601 | T | G | 2 | a0001c0002t0002g0181 a0001c0002t0002g0182 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2806+360A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057601 | |||||||
chr9:19057772 | A | C | 15 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0104 others(12): Show |
17 | HG00609.hp2 HG01123.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2806+189T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057772 | |||||||
chr9:19057779 | T | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2806+182A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057779 | |||||||
chr9:19057854 | A | G | 1 | a0001c0002t0002g0066 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2806+107T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057854 | |||||||
chr9:19057878 | C | T | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2806+83G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057878 | |||||||
chr9:19057912 | G | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2806+49C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 16/16 | chr9 | 19057912 | |||||||
chr9:19059157 | T | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1766-156A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059157 | |||||||
chr9:19059287 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1766-286C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059287 | |||||||
chr9:19059375 | A | T | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1766-374T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059375 | |||||||
chr9:19059377 | T | C | 3 | a0006c0014t0022g0124 a0006c0016t0014g0123 a0006c0016t0014g0125 |
3 | HG02109.hp2 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1766-376A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059377 | |||||||
chr9:19059397 | T | C | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1766-396A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059397 | |||||||
chr9:19059399 | A | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | NA18950.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1766-398T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059399 | |||||||
chr9:19059553 | A | G | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1765+535T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059553 | |||||||
chr9:19059658 | G | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1765+430C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059658 | |||||||
chr9:19059680 | G | A | 21 | a0003c0006t0003g0013 a0003c0006t0003g0014 a0003c0006t0003g0135 others(18): Show |
23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.1765+408C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059680 | |||||||
chr9:19059702 | T | G | 1 | a0001c0012t0004g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1765+386A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059702 | |||||||
chr9:19059765 | T | C | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1765+323A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059765 | |||||||
chr9:19059771 | T | C | 139 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(136): Show |
147 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1765+317A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059771 | |||||||
chr9:19059867 | G | C | 23 | a0003c0006t0003g0013 a0003c0006t0003g0014 a0003c0006t0003g0135 others(20): Show |
25 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1765+221C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059867 | |||||||
chr9:19059892 | T | C | 2 | a0006c0016t0014g0123 a0006c0016t0014g0125 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1765+196A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059892 | |||||||
chr9:19059896 | T | A | 2 | a0002c0003t0005g0341 a0002c0003t0005g0347 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1765+192A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19059896 | |||||||
chr9:19060048 | C | T | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1765+40G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 15/16 | chr9 | 19060048 | |||||||
chr9:19060233 | A | G | 2 | a0001c0004t0003g0298 a0001c0004t0003g0301 |
2 | HG01192.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1630-10T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060233 | |||||||
chr9:19060370 | C | A | 150 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(147): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1630-147G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060370 | |||||||
chr9:19060371 | A | G | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1630-148T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060371 | |||||||
chr9:19060372 | A | T | 40 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(37): Show |
43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.1630-149T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060372 | |||||||
chr9:19060410 | G | C | 1 | a0001c0020t0001g0018 | 2 | HG01069.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1630-187C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060410 | |||||||
chr9:19060417 | G | C | 10 | a0001c0005t0004g0012 a0001c0005t0004g0108 a0001c0005t0004g0109 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1630-194C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060417 | |||||||
chr9:19060425 | G | A | 150 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(147): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1630-202C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060425 | |||||||
chr9:19060556 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1630-333G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060556 | |||||||
chr9:19060828 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1630-605G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060828 | |||||||
chr9:19060891 | G | A | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1630-668C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060891 | |||||||
chr9:19060962 | G | T | 1 | a0001c0020t0001g0018 | 2 | HG01069.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1630-739C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19060962 | |||||||
chr9:19061118 | C | T | 1 | a0003c0006t0003g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1630-895G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061118 | |||||||
chr9:19061159 | C | T | 138 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(135): Show |
146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1630-936G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061159 | |||||||
chr9:19061249 | G | A | 1 | a0001c0002t0002g0080 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1630-1026C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061249 | |||||||
chr9:19061250 | C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1630-1027G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061250 | |||||||
chr9:19061275 | T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1630-1052A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061275 | |||||||
chr9:19061289 | C | T | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1630-1066G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061289 | |||||||
chr9:19061360 | C | T | 138 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(135): Show |
146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1630-1137G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061360 | |||||||
chr9:19061466 | G | C | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1630-1243C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061466 | |||||||
chr9:19061626 | C | T | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1629+1382G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061626 | |||||||
chr9:19061640 | A | G | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(267): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1629+1368T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061640 | |||||||
chr9:19061660 | T | C | 150 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(147): Show |
158 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1629+1348A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061660 | |||||||
chr9:19061661 | C | T | 138 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(135): Show |
146 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.1629+1347G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061661 | |||||||
chr9:19061688 | A | T | 2 | a0011c0018t0010g0102 a0011c0018t0010g0103 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1629+1320T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061688 | |||||||
chr9:19061761 | G | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1629+1247C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061761 | |||||||
chr9:19061767 | C | T | 3 | a0001c0002t0002g0037 a0001c0002t0002g0044 a0001c0002t0002g0047 |
3 | NA18980.hp1 NA18993.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1629+1241G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061767 | |||||||
chr9:19061859 | C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1629+1149G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061859 | |||||||
chr9:19061943 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+1065A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061943 | |||||||
chr9:19061986 | G | C | 1 | a0004c0008t0006g0365 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1629+1022C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19061986 | |||||||
chr9:19062120 | C | G | 3 | a0010c0021t0003g0293 a0010c0021t0003g0307 a0017c0039t0003g0308 |
3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1629+888G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062120 | |||||||
chr9:19062168 | T | C | 3 | a0010c0021t0003g0293 a0010c0021t0003g0307 a0017c0039t0003g0308 |
3 | HG02717.hp2 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1629+840A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062168 | |||||||
chr9:19062280 | A | T | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1629+728T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062280 | |||||||
chr9:19062350 | A | G | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+658T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062350 | |||||||
chr9:19062355 | A | G | 33 | a0001c0004t0003g0106 a0001c0005t0004g0012 a0001c0005t0004g0098 others(30): Show |
34 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1629+653T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062355 | |||||||
chr9:19062460 | G | C | 1 | a0001c0007t0002g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1629+548C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062460 | |||||||
chr9:19062512 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+496A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062512 | |||||||
chr9:19062534 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0216 a0001c0001t0001g0242 |
5 | HG03017.hp1 HG03710.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+474C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062534 | |||||||
chr9:19062583 | C | G | 114 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(111): Show |
120 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(117): Show |
intron_variant | MODIFIER | c.1629+425G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062583 | |||||||
chr9:19062609 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0020g0241 |
3 | NA18999.hp2 NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1629+399G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062609 | |||||||
chr9:19062691 | T | G | 5 | a0002c0003t0007g0334 a0002c0003t0007g0335 a0002c0003t0007g0336 others(2): Show |
5 | HG02965.hp2 HG03041.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1629+317A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062691 | |||||||
chr9:19062773 | C | T | 6 | a0001c0001t0001g0214 a0001c0001t0001g0248 a0001c0001t0001g0249 others(3): Show |
6 | HG02257.hp2 HG03041.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1629+235G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062773 | |||||||
chr9:19062876 | T | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1629+132A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062876 | |||||||
chr9:19062885 | C | G | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1629+123G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062885 | |||||||
chr9:19062899 | C | G | 1 | a0001c0001t0001g0021 | 2 | NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1629+109G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062899 | |||||||
chr9:19062944 | A | G | 167 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(164): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1629+64T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 14/16 | chr9 | 19062944 | |||||||
chr9:19063323 | C | G | 2 | a0001c0002t0002g0034 a0001c0002t0002g0060 |
2 | HG00673.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1444-130G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063323 | |||||||
chr9:19063368 | G | A | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1443+146C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063368 | |||||||
chr9:19063369 | A | AAT | 168 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(165): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1443+143_1443+144d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063369 | |||||||
chr9:19063379 | G | T | 1 | a0001c0005t0004g0109 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1443+135C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063379 | |||||||
chr9:19063392 | A | AT | 3 | a0001c0001t0001g0017 a0001c0001t0001g0229 a0001c0001t0001g0233 |
4 | HG01884.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443+121dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 13/16 | chr9 | 19063392 | |||||||
chr9:19063592 | A | G | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1377-12T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063592 | |||||||
chr9:19063632 | T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377-52A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063632 | |||||||
chr9:19063767 | A | G | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1377-187T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063767 | |||||||
chr9:19063848 | T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1377-268A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063848 | |||||||
chr9:19063931 | T | G | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1377-351A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063931 | |||||||
chr9:19063970 | A | AT | 15 | a0001c0001t0001g0252 a0001c0002t0002g0011 a0001c0002t0002g0181 others(12): Show |
16 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1377-391dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | |||||||
chr9:19063970 | A | ATT | 6 | a0006c0014t0010g0277 a0006c0014t0022g0124 a0006c0016t0014g0123 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1377-392_1377-391d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | |||||||
chr9:19063970 | A | ATTT | 78 | a0001c0005t0004g0012 a0001c0005t0004g0098 a0001c0005t0004g0107 others(75): Show |
81 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1377-393_1377-391d others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | |||||||
chr9:19063970 | A | ATTTT | 25 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(22): Show |
27 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1377-394_1377-391d others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063970 | |||||||
chr9:19063972 | T | TTTA | 43 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(40): Show |
46 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.1377-393_1377-392i others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063972 | |||||||
chr9:19063975 | T | A | 1 | a0001c0002t0002g0179 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1377-395A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063975 | |||||||
chr9:19063977 | T | A | 2 | a0001c0005t0003g0297 a0006c0014t0025g0126 |
2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1377-397A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19063977 | |||||||
chr9:19064036 | T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1377-456A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064036 | |||||||
chr9:19064053 | C | T | 1 | a0005c0036t0002g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1377-473G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064053 | |||||||
chr9:19064058 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG00099.hp1 HG01361.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1377-478G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064058 | |||||||
chr9:19064070 | C | A | 140 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(137): Show |
148 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.1377-490G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064070 | |||||||
chr9:19064131 | G | C | 151 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(148): Show |
159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1377-551C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064131 | |||||||
chr9:19064192 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1377-612G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064192 | |||||||
chr9:19064299 | T | C | 2 | a0001c0004t0003g0289 a0001c0004t0003g0290 |
2 | HG00609.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1377-719A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064299 | |||||||
chr9:19064359 | T | C | 1 | a0001c0007t0002g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1377-779A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064359 | |||||||
chr9:19064391 | G | C | 1 | a0001c0019t0015g0119 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1377-811C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064391 | |||||||
chr9:19064423 | T | C | 2 | a0011c0018t0010g0102 a0011c0018t0010g0103 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1377-843A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064423 | |||||||
chr9:19064691 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1377-1111A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064691 | |||||||
chr9:19064699 | T | G | 168 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(165): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1377-1119A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064699 | |||||||
chr9:19064735 | C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1377-1155G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19064735 | |||||||
chr9:19065061 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1377-1481G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065061 | |||||||
chr9:19065154 | G | C | 30 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(27): Show |
32 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1377-1574C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065154 | |||||||
chr9:19065297 | T | C | 164 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(161): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1377-1717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065297 | |||||||
chr9:19065510 | CA | C | 165 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(162): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1377-1931delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065510 | |||||||
chr9:19065528 | G | A | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1377-1948C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065528 | |||||||
chr9:19065614 | G | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377-2034C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065614 | |||||||
chr9:19065705 | G | A | 1 | a0001c0005t0004g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1377-2125C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065705 | |||||||
chr9:19065713 | C | T | 2 | a0001c0001t0001g0234 a0001c0035t0001g0240 |
2 | NA18980.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1377-2133G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065713 | |||||||
chr9:19065714 | G | A | 2 | a0001c0001t0001g0223 a0012c0042t0016g0318 |
2 | HG01891.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1377-2134C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065714 | |||||||
chr9:19065759 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1377-2179A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065759 | |||||||
chr9:19065827 | A | G | 164 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(161): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1377-2247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065827 | |||||||
chr9:19065836 | C | T | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377-2256G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065836 | |||||||
chr9:19065848 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1377-2268T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065848 | |||||||
chr9:19065864 | T | C | 164 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(161): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1377-2284A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065864 | |||||||
chr9:19065935 | A | AT | 13 | a0001c0001t0001g0027 a0001c0001t0001g0247 a0001c0001t0001g0255 others(10): Show |
13 | HG00544.hp1 HG01175.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1377-2356dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065935 | |||||||
chr9:19065935 | AT | A | 61 | a0001c0001t0001g0178 a0001c0001t0001g0188 a0001c0001t0001g0220 others(58): Show |
64 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.1377-2356delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19065935 | |||||||
chr9:19066048 | G | A | 36 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(33): Show |
38 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1377-2468C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066048 | |||||||
chr9:19066084 | G | A | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1377-2504C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066084 | |||||||
chr9:19066102 | A | C | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1377-2522T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066102 | |||||||
chr9:19066117 | A | G | 164 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(161): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1377-2537T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066117 | |||||||
chr9:19066137 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1377-2557A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066137 | |||||||
chr9:19066150 | G | T | 3 | a0001c0005t0004g0111 a0001c0005t0004g0112 a0001c0005t0004g0116 |
3 | HG02486.hp1 HG03486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1377-2570C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066150 | |||||||
chr9:19066193 | C | A | 1 | a0001c0002t0002g0015 | 2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1377-2613G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066193 | |||||||
chr9:19066553 | C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1377-2973G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066553 | |||||||
chr9:19066579 | CCA | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377-3001_1377-300 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066579 | |||||||
chr9:19066582 | C | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1377-3002G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066582 | |||||||
chr9:19066687 | C | T | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1377-3107G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066687 | |||||||
chr9:19066698 | G | C | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1377-3118C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066698 | |||||||
chr9:19066811 | T | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1377-3231A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066811 | |||||||
chr9:19066830 | C | CA | 115 | a0001c0001t0001g0211 a0001c0001t0001g0219 a0001c0001t0001g0232 others(112): Show |
119 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1377-3251dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | |||||||
chr9:19066830 | C | CAA | 7 | a0001c0004t0003g0290 a0001c0005t0008g0327 a0001c0005t0008g0328 others(4): Show |
7 | HG01934.hp2 HG02135.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1377-3252_1377-325 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | |||||||
chr9:19066830 | CAAAAAA | C | 38 | a0001c0005t0023g0095 a0002c0003t0005g0007 a0002c0003t0005g0330 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1377-3256_1377-325 others(10): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19066830 | |||||||
chr9:19067005 | C | CA | 7 | a0001c0002t0002g0048 a0001c0007t0002g0163 a0001c0024t0021g0177 others(4): Show |
7 | HG02055.hp2 HG02698.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1376+3213dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067005 | |||||||
chr9:19067103 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+3116A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067103 | |||||||
chr9:19067131 | T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1376+3088A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067131 | |||||||
chr9:19067149 | T | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+3070A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067149 | |||||||
chr9:19067214 | C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+3005G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067214 | |||||||
chr9:19067238 | A | G | 1 | a0001c0005t0004g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1376+2981T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067238 | |||||||
chr9:19067243 | A | G | 2 | a0001c0026t0028g0170 a0023c0041t0001g0317 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1376+2976T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067243 | |||||||
chr9:19067260 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+2959A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067260 | |||||||
chr9:19067320 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1376+2899T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067320 | |||||||
chr9:19067362 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1376+2857G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067362 | |||||||
chr9:19067432 | T | C | 1 | a0002c0003t0005g0358 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1376+2787A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067432 | |||||||
chr9:19067483 | G | A | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1376+2736C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067483 | |||||||
chr9:19067510 | C | T | 2 | a0001c0010t0002g0008 a0001c0010t0002g0040 |
3 | NA18981.hp2 NA19086.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1376+2709G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067510 | |||||||
chr9:19067694 | G | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1376+2525C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067694 | |||||||
chr9:19067757 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1376+2462G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067757 | |||||||
chr9:19067765 | C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1376+2454G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067765 | |||||||
chr9:19067775 | G | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+2444C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067775 | |||||||
chr9:19067835 | A | G | 165 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(162): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1376+2384T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067835 | |||||||
chr9:19067867 | T | G | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+2352A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067867 | |||||||
chr9:19067997 | CA | C | 5 | a0002c0003t0005g0339 a0002c0003t0005g0344 a0002c0003t0005g0345 others(2): Show |
5 | HG02155.hp1 HG03453.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.1376+2221delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067997 | |||||||
chr9:19067998 | A | C | 2 | a0005c0009t0001g0228 a0005c0009t0001g0239 |
2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1376+2221T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19067998 | |||||||
chr9:19068053 | A | G | 166 | a0001c0002t0018g0171 a0001c0004t0003g0022 a0001c0004t0003g0023 others(163): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1376+2166T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068053 | |||||||
chr9:19068132 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1376+2087C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068132 | |||||||
chr9:19068151 | T | C | 2 | a0001c0001t0001g0257 a0015c0032t0001g0224 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1376+2068A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068151 | |||||||
chr9:19068252 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00323.hp2 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1376+1967G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068252 | |||||||
chr9:19068254 | CCAGGTCC others(113): Show |
C | 3 | a0002c0003t0005g0332 a0002c0003t0005g0360 a0020c0028t0005g0340 |
3 | NA19066.hp1 NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1376+1845_1376+196 others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068254 | |||||||
chr9:19068257 | G | A | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1376+1962C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068257 | |||||||
chr9:19068320 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1376+1899A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068320 | |||||||
chr9:19068320 | T | G | 45 | a0001c0005t0023g0095 a0001c0007t0002g0137 a0001c0007t0002g0139 others(42): Show |
47 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1376+1899A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068320 | |||||||
chr9:19068374 | A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1376+1845T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068374 | |||||||
chr9:19068495 | C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+1724G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068495 | |||||||
chr9:19068507 | T | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1376+1712A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068507 | |||||||
chr9:19068510 | C | A | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1376+1709G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068510 | |||||||
chr9:19068581 | C | T | 121 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(118): Show |
127 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.1376+1638G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068581 | |||||||
chr9:19068667 | C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1376+1552G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068667 | |||||||
chr9:19068714 | T | TA | 83 | a0001c0001t0001g0259 a0001c0004t0003g0022 a0001c0004t0003g0023 others(80): Show |
87 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(84): Show |
intron_variant | MODIFIER | c.1376+1504dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068714 | |||||||
chr9:19068804 | T | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+1415A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068804 | |||||||
chr9:19068845 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1376+1374T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068845 | |||||||
chr9:19068907 | T | C | 1 | a0001c0007t0002g0140 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1376+1312A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068907 | |||||||
chr9:19068952 | A | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1376+1267T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068952 | |||||||
chr9:19068966 | T | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1376+1253A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19068966 | |||||||
chr9:19069017 | C | T | 1 | a0017c0039t0003g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1376+1202G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069017 | |||||||
chr9:19069120 | C | T | 1 | a0018c0022t0026g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1376+1099G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069120 | |||||||
chr9:19069411 | G | A | 112 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(109): Show |
118 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.1376+808C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069411 | |||||||
chr9:19069481 | G | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
127 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1376+738C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069481 | |||||||
chr9:19069487 | G | A | 72 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(69): Show |
76 | HG00609.hp2 HG01081.hp1 HG01123.hp2 others(73): Show |
intron_variant | MODIFIER | c.1376+732C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069487 | |||||||
chr9:19069566 | G | C | 1 | a0001c0002t0002g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1376+653C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069566 | |||||||
chr9:19069653 | C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1376+566G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069653 | |||||||
chr9:19069827 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+392T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069827 | |||||||
chr9:19069863 | C | A | 81 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(78): Show |
85 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(82): Show |
intron_variant | MODIFIER | c.1376+356G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069863 | |||||||
chr9:19069913 | C | T | 118 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(115): Show |
124 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(121): Show |
intron_variant | MODIFIER | c.1376+306G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069913 | |||||||
chr9:19069972 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19069972 | |||||||
chr9:19070108 | C | G | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1376+111G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070108 | |||||||
chr9:19070132 | G | A | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1376+87C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070132 | |||||||
chr9:19070133 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+86G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070133 | |||||||
chr9:19070193 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1376+26T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 12/16 | chr9 | 19070193 | |||||||
chr9:19070391 | C | G | 3 | a0006c0014t0010g0277 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG03453.hp1 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1295-91G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070391 | |||||||
chr9:19070474 | A | G | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1295-174T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070474 | |||||||
chr9:19070483 | G | C | 1 | a0004c0008t0006g0364 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1295-183C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070483 | |||||||
chr9:19070488 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-188G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070488 | |||||||
chr9:19070609 | C | G | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1295-309G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070609 | |||||||
chr9:19070615 | C | T | 4 | a0001c0002t0002g0030 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): Show |
4 | NA18963.hp1 NA18986.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295-315G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070615 | |||||||
chr9:19070619 | C | T | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1295-319G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070619 | |||||||
chr9:19070664 | T | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-364A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19070664 | |||||||
chr9:19071205 | A | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1295-905T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071205 | |||||||
chr9:19071237 | A | G | 48 | a0001c0001t0001g0017 a0001c0002t0002g0179 a0001c0005t0004g0132 others(45): Show |
51 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.1295-937T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071237 | |||||||
chr9:19071304 | G | C | 1 | a0002c0030t0005g0321 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1295-1004C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071304 | |||||||
chr9:19071366 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1295-1066G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071366 | |||||||
chr9:19071404 | A | G | 1 | a0001c0002t0002g0084 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1295-1104T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071404 | |||||||
chr9:19071573 | C | CT | 46 | a0001c0002t0002g0079 a0001c0002t0002g0083 a0001c0002t0002g0091 others(43): Show |
47 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(44): Show |
intron_variant | MODIFIER | c.1295-1274dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | |||||||
chr9:19071573 | C | CTT | 8 | a0001c0007t0002g0153 a0003c0006t0003g0013 a0003c0006t0003g0148 others(5): Show |
9 | HG00642.hp2 HG01081.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-1275_1295-127 others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | |||||||
chr9:19071573 | CT | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
236 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1295-1274delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071573 | |||||||
chr9:19071617 | C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1295-1317G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071617 | |||||||
chr9:19071640 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0275 |
2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1295-1340G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071640 | |||||||
chr9:19071654 | G | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295-1354C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071654 | |||||||
chr9:19071658 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1295-1358G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071658 | |||||||
chr9:19071833 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1295-1533C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071833 | |||||||
chr9:19071925 | C | T | 1 | a0001c0004t0003g0282 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1295-1625G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071925 | |||||||
chr9:19071979 | G | A | 1 | a0020c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1295-1679C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071979 | |||||||
chr9:19071996 | G | C | 2 | a0011c0018t0010g0102 a0011c0018t0010g0103 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1295-1696C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19071996 | |||||||
chr9:19072014 | G | GCCAACAT others(7): Show |
8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-1715_1295-171 others(18): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072014 | |||||||
chr9:19072095 | T | C | 1 | a0001c0005t0004g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1295-1795A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072095 | |||||||
chr9:19072175 | A | G | 1 | a0004c0008t0006g0363 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1295-1875T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072175 | |||||||
chr9:19072190 | C | CA | 156 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0002t0018g0171 others(153): Show |
164 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1295-1891dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072190 | |||||||
chr9:19072220 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1295-1920T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072220 | |||||||
chr9:19072248 | A | C | 153 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0002t0018g0171 others(150): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1295-1948T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072248 | |||||||
chr9:19072289 | G | T | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1295-1989C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072289 | |||||||
chr9:19072292 | C | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1295-1992G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072292 | |||||||
chr9:19072294 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-1994G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072294 | |||||||
chr9:19072386 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0269 |
3 | NA18957.hp2 NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1295-2086C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072386 | |||||||
chr9:19072423 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1295-2123C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072423 | |||||||
chr9:19072508 | CA | C | 13 | a0001c0002t0002g0087 a0001c0005t0004g0109 a0001c0005t0023g0095 others(10): Show |
13 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1295-2209delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072508 | |||||||
chr9:19072586 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-2286G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072586 | |||||||
chr9:19072600 | G | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1295-2300C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072600 | |||||||
chr9:19072629 | C | G | 2 | a0001c0002t0018g0171 a0001c0024t0021g0177 |
2 | HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1295-2329G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072629 | |||||||
chr9:19072747 | T | C | 1 | a0003c0006t0003g0146 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1295-2447A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072747 | |||||||
chr9:19072926 | C | G | 112 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0004t0003g0022 others(109): Show |
118 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1295-2626G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19072926 | |||||||
chr9:19073025 | C | A | 1 | a0005c0036t0002g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1295-2725G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073025 | |||||||
chr9:19073034 | A | C | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1295-2734T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073034 | |||||||
chr9:19073180 | T | C | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1295-2880A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073180 | |||||||
chr9:19073200 | G | C | 1 | a0002c0003t0005g0346 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1295-2900C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073200 | |||||||
chr9:19073246 | T | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1295-2946A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073246 | |||||||
chr9:19073422 | G | GA | 111 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(108): Show |
117 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1295-3123dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073422 | |||||||
chr9:19073447 | T | C | 34 | a0001c0004t0003g0106 a0001c0005t0003g0114 a0001c0005t0004g0012 others(31): Show |
35 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1295-3147A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073447 | |||||||
chr9:19073474 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0233 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1294+3128C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073474 | |||||||
chr9:19073642 | C | A | 10 | a0001c0005t0023g0095 a0004c0008t0006g0025 a0004c0008t0006g0362 others(7): Show |
10 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294+2960G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073642 | |||||||
chr9:19073654 | A | C | 1 | a0001c0005t0004g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1294+2948T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073654 | |||||||
chr9:19073912 | A | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1294+2690T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073912 | |||||||
chr9:19073922 | T | G | 1 | a0004c0008t0006g0367 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1294+2680A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073922 | |||||||
chr9:19073970 | A | G | 10 | a0001c0005t0023g0095 a0004c0008t0006g0025 a0004c0008t0006g0362 others(7): Show |
10 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294+2632T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19073970 | |||||||
chr9:19074073 | C | A | 1 | a0009c0015t0003g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1294+2529G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074073 | |||||||
chr9:19074115 | A | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+2487T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074115 | |||||||
chr9:19074140 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1294+2462C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074140 | |||||||
chr9:19074195 | C | T | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1294+2407G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074195 | |||||||
chr9:19074220 | C | T | 3 | a0001c0005t0004g0107 a0001c0005t0004g0134 a0019c0040t0004g0316 |
3 | NA18990.hp1 NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1294+2382G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074220 | |||||||
chr9:19074244 | C | CA | 12 | a0002c0003t0005g0342 a0002c0003t0005g0349 a0002c0003t0005g0354 others(9): Show |
12 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1294+2357dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074244 | |||||||
chr9:19074333 | G | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+2269C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074333 | |||||||
chr9:19074342 | G | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1294+2260C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074342 | |||||||
chr9:19074355 | T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1294+2247A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074355 | |||||||
chr9:19074364 | C | T | 1 | a0003c0006t0003g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1294+2238G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074364 | |||||||
chr9:19074416 | C | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1294+2186G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074416 | |||||||
chr9:19074428 | G | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+2174C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074428 | |||||||
chr9:19074492 | G | A | 1 | a0002c0003t0005g0356 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1294+2110C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074492 | |||||||
chr9:19074540 | A | G | 164 | a0001c0002t0018g0171 a0001c0004t0003g0022 a0001c0004t0003g0023 others(161): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1294+2062T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074540 | |||||||
chr9:19074561 | T | C | 1 | a0001c0004t0003g0295 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1294+2041A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074561 | |||||||
chr9:19074742 | A | G | 51 | a0001c0005t0023g0095 a0001c0007t0002g0137 a0001c0007t0002g0139 others(48): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1294+1860T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074742 | |||||||
chr9:19074788 | A | T | 51 | a0001c0005t0023g0095 a0001c0007t0002g0137 a0001c0007t0002g0139 others(48): Show |
53 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1294+1814T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074788 | |||||||
chr9:19074812 | C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1294+1790G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074812 | |||||||
chr9:19074822 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.1294+1780G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19074822 | |||||||
chr9:19075001 | A | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1294+1601T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075001 | |||||||
chr9:19075327 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1294+1275A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075327 | |||||||
chr9:19075632 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1294+970G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075632 | |||||||
chr9:19075664 | C | T | 3 | a0002c0003t0005g0342 a0002c0003t0005g0349 a0002c0003t0005g0354 |
3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1294+938G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075664 | |||||||
chr9:19075675 | C | T | 1 | a0002c0003t0007g0333 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1294+927G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075675 | |||||||
chr9:19075713 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1294+889C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075713 | |||||||
chr9:19075737 | C | T | 1 | a0002c0003t0007g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1294+865G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075737 | |||||||
chr9:19075799 | C | CA | 39 | a0001c0001t0001g0253 a0002c0003t0005g0007 a0002c0003t0005g0330 others(36): Show |
41 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1294+802dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075799 | |||||||
chr9:19075860 | G | C | 1 | a0001c0004t0003g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1294+742C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075860 | |||||||
chr9:19075915 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+687G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075915 | |||||||
chr9:19075961 | A | G | 3 | a0001c0004t0003g0310 a0008c0017t0013g0172 a0008c0017t0013g0173 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1294+641T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075961 | |||||||
chr9:19075970 | A | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+632T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075970 | |||||||
chr9:19075975 | A | AC | 10 | a0001c0001t0001g0243 a0001c0001t0001g0260 a0001c0001t0001g0268 others(7): Show |
10 | HG00423.hp2 HG02273.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1294+626_1294+627i others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075975 | |||||||
chr9:19075975 | A | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1294+627T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19075975 | |||||||
chr9:19076012 | G | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1294+590C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076012 | |||||||
chr9:19076083 | G | T | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1294+519C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076083 | |||||||
chr9:19076096 | A | G | 42 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+506T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076096 | |||||||
chr9:19076102 | G | A | 42 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+500C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076102 | |||||||
chr9:19076169 | G | A | 42 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1294+433C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076169 | |||||||
chr9:19076196 | CA | C | 125 | a0001c0002t0002g0038 a0001c0002t0018g0171 a0001c0005t0003g0114 others(122): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1294+405delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076196 | |||||||
chr9:19076208 | A | T | 43 | a0001c0002t0002g0049 a0001c0007t0002g0137 a0001c0007t0002g0139 others(40): Show |
45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.1294+394T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076208 | |||||||
chr9:19076313 | G | A | 2 | a0001c0001t0001g0257 a0015c0032t0001g0224 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1294+289C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076313 | |||||||
chr9:19076315 | C | T | 3 | a0002c0003t0005g0332 a0002c0003t0005g0360 a0020c0028t0005g0340 |
3 | NA19066.hp1 NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1294+287G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076315 | |||||||
chr9:19076316 | T | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1294+286A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076316 | |||||||
chr9:19076355 | A | G | 3 | a0002c0003t0005g0342 a0002c0003t0005g0349 a0002c0003t0005g0354 |
3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1294+247T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076355 | |||||||
chr9:19076465 | A | T | 1 | a0001c0012t0004g0099 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1294+137T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076465 | |||||||
chr9:19076530 | G | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0275 |
2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1294+72C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 11/16 | chr9 | 19076530 | |||||||
chr9:19076766 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192-62T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076766 | |||||||
chr9:19076792 | CT | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192-89delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076792 | |||||||
chr9:19076857 | T | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0086 |
4 | HG00597.hp2 NA18964.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1192-153A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076857 | |||||||
chr9:19076883 | G | A | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1192-179C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19076883 | |||||||
chr9:19077033 | A | G | 346 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(343): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1192-329T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077033 | |||||||
chr9:19077095 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1192-391G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077095 | |||||||
chr9:19077120 | A | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1192-416T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077120 | |||||||
chr9:19077133 | C | T | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1192-429G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077133 | |||||||
chr9:19077418 | C | A | 11 | a0001c0004t0003g0104 a0001c0004t0003g0105 a0001c0004t0003g0286 others(8): Show |
11 | HG00609.hp2 HG01123.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1192-714G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077418 | |||||||
chr9:19077423 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1192-719A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077423 | |||||||
chr9:19077472 | C | T | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+704G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077472 | |||||||
chr9:19077490 | G | A | 1 | a0001c0002t0002g0081 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1191+686C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077490 | |||||||
chr9:19077492 | G | A | 30 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(27): Show |
32 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1191+684C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077492 | |||||||
chr9:19077505 | A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1191+671T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077505 | |||||||
chr9:19077516 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0020g0241 |
3 | NA18999.hp2 NA19004.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1191+660A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077516 | |||||||
chr9:19077612 | C | T | 2 | a0001c0001t0001g0027 a0001c0037t0001g0311 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1191+564G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077612 | |||||||
chr9:19077621 | A | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+555T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077621 | |||||||
chr9:19077636 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+540G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077636 | |||||||
chr9:19077824 | G | A | 1 | a0001c0002t0002g0065 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1191+352C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077824 | |||||||
chr9:19077872 | G | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+304C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077872 | |||||||
chr9:19077919 | G | A | 3 | a0001c0026t0028g0170 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1191+257C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077919 | |||||||
chr9:19077922 | T | G | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1191+254A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19077922 | |||||||
chr9:19078012 | G | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1191+164C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078012 | |||||||
chr9:19078118 | C | CA | 7 | a0001c0001t0001g0192 a0001c0004t0003g0024 a0001c0004t0003g0299 others(4): Show |
8 | HG00735.hp1 HG01433.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1191+57dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078118 | |||||||
chr9:19078133 | A | C | 3 | a0001c0001t0001g0312 a0008c0017t0013g0172 a0008c0017t0013g0173 |
3 | HG01515.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1191+43T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078133 | |||||||
chr9:19078144 | G | A | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1191+32C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 10/16 | chr9 | 19078144 | |||||||
chr9:19078402 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
14 | HG00544.hp1 HG00609.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1065-100A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078402 | |||||||
chr9:19078404 | G | C | 2 | a0003c0006t0003g0158 a0003c0006t0003g0165 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1065-102C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078404 | |||||||
chr9:19078509 | C | T | 1 | a0001c0005t0004g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1065-207G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078509 | |||||||
chr9:19078517 | G | A | 3 | a0001c0002t0002g0181 a0001c0002t0002g0182 a0001c0005t0003g0297 |
3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1065-215C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078517 | |||||||
chr9:19078584 | T | C | 1 | a0001c0002t0002g0087 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1065-282A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078584 | |||||||
chr9:19078645 | G | A | 3 | a0001c0026t0028g0170 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1065-343C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078645 | |||||||
chr9:19078781 | G | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1065-479C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078781 | |||||||
chr9:19078801 | A | T | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1065-499T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078801 | |||||||
chr9:19078845 | TA | T | 125 | a0001c0002t0002g0037 a0001c0002t0002g0041 a0001c0002t0002g0043 others(122): Show |
131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.1065-544delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078845 | |||||||
chr9:19078845 | TAA | T | 29 | a0001c0007t0024g0162 a0002c0003t0005g0348 a0003c0006t0003g0013 others(26): Show |
31 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1065-545_1065-544d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078845 | |||||||
chr9:19078847 | A | T | 2 | a0001c0004t0003g0281 a0001c0004t0003g0282 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1065-545T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078847 | |||||||
chr9:19078937 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1065-635T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19078937 | |||||||
chr9:19079078 | C | G | 1 | a0005c0009t0001g0238 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1065-776G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079078 | |||||||
chr9:19079119 | G | A | 4 | a0001c0012t0004g0099 a0001c0012t0004g0100 a0001c0012t0004g0101 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1065-817C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079119 | |||||||
chr9:19079160 | G | A | 2 | a0001c0002t0002g0066 a0001c0002t0002g0067 |
2 | HG03654.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1065-858C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079160 | |||||||
chr9:19079164 | C | CA | 9 | a0001c0001t0001g0191 a0001c0001t0001g0236 a0001c0001t0001g0247 others(6): Show |
9 | HG01175.hp1 HG02055.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1065-863dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079164 | |||||||
chr9:19079164 | CA | C | 31 | a0001c0005t0004g0122 a0001c0007t0024g0162 a0003c0006t0003g0013 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1065-863delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079164 | |||||||
chr9:19079201 | T | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1065-899A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079201 | |||||||
chr9:19079377 | G | A | 71 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(68): Show |
75 | HG00609.hp2 HG01081.hp1 HG01123.hp2 others(72): Show |
intron_variant | MODIFIER | c.1065-1075C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079377 | |||||||
chr9:19079506 | C | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1064+973G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079506 | |||||||
chr9:19079550 | T | C | 1 | a0001c0002t0002g0082 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1064+929A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079550 | |||||||
chr9:19079678 | G | A | 4 | a0001c0012t0004g0099 a0001c0012t0004g0100 a0001c0012t0004g0101 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064+801C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079678 | |||||||
chr9:19079720 | T | C | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064+759A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079720 | |||||||
chr9:19079766 | G | C | 3 | a0001c0002t0002g0181 a0001c0002t0002g0182 a0001c0005t0003g0297 |
3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1064+713C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079766 | |||||||
chr9:19079800 | G | A | 1 | a0001c0005t0003g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1064+679C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079800 | |||||||
chr9:19079828 | G | A | 28 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(25): Show |
30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1064+651C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079828 | |||||||
chr9:19079831 | A | C | 29 | a0001c0005t0023g0095 a0001c0007t0024g0162 a0003c0006t0003g0013 others(26): Show |
31 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1064+648T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079831 | |||||||
chr9:19079851 | A | G | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+628T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079851 | |||||||
chr9:19079890 | A | G | 2 | a0002c0003t0005g0332 a0002c0003t0005g0360 |
2 | NA19072.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1064+589T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079890 | |||||||
chr9:19079891 | G | A | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064+588C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079891 | |||||||
chr9:19079941 | G | A | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1064+538C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19079941 | |||||||
chr9:19080038 | G | A | 1 | a0003c0006t0003g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1064+441C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080038 | |||||||
chr9:19080056 | C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1064+423G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080056 | |||||||
chr9:19080125 | G | C | 1 | a0001c0029t0001g0227 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1064+354C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080125 | |||||||
chr9:19080138 | C | A | 3 | a0001c0002t0002g0033 a0001c0002t0002g0035 a0001c0002t0002g0077 |
3 | NA18948.hp2 NA18967.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1064+341G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080138 | |||||||
chr9:19080161 | C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1064+318G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080161 | |||||||
chr9:19080174 | C | CA | 47 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0192 others(44): Show |
49 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1064+304dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | |||||||
chr9:19080174 | C | CAA | 58 | a0001c0001t0001g0253 a0001c0001t0001g0263 a0001c0004t0003g0022 others(55): Show |
62 | HG01081.hp1 HG01192.hp2 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.1064+303_1064+304d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | |||||||
chr9:19080174 | C | CAAA | 14 | a0001c0001t0001g0247 a0001c0004t0003g0286 a0001c0004t0003g0288 others(11): Show |
14 | HG00609.hp2 HG01123.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1064+302_1064+304d others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | |||||||
chr9:19080174 | CA | C | 8 | a0001c0001t0001g0174 a0001c0001t0001g0197 a0001c0001t0001g0220 others(5): Show |
8 | HG01516.hp2 HG02970.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064+304delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080174 | |||||||
chr9:19080328 | A | G | 3 | a0008c0017t0013g0172 a0008c0017t0013g0173 a0012c0042t0016g0318 |
3 | HG01891.hp2 HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1064+151T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080328 | |||||||
chr9:19080354 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0020g0241 a0001c0002t0018g0171 others(162): Show |
174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1064+125T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080354 | |||||||
chr9:19080388 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1064+91G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 9/16 | chr9 | 19080388 | |||||||
chr9:19080708 | A | G | 3 | a0001c0002t0002g0181 a0001c0002t0002g0182 a0001c0005t0003g0297 |
3 | HG02809.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.871-36T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080708 | |||||||
chr9:19080752 | T | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-80A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080752 | |||||||
chr9:19080799 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.871-127C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080799 | |||||||
chr9:19080824 | C | T | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.871-152G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080824 | |||||||
chr9:19080844 | G | C | 1 | a0001c0005t0008g0329 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.871-172C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080844 | |||||||
chr9:19080863 | G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.871-191C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080863 | |||||||
chr9:19080880 | C | T | 4 | a0001c0011t0004g0128 a0001c0011t0004g0129 a0001c0011t0004g0130 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.871-208G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080880 | |||||||
chr9:19080933 | G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.871-261C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080933 | |||||||
chr9:19080986 | C | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.871-314G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080986 | |||||||
chr9:19080987 | G | A | 1 | a0001c0002t0002g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.871-315C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19080987 | |||||||
chr9:19081096 | CG | C | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.871-425delC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081096 | |||||||
chr9:19081117 | C | T | 39 | a0001c0001t0001g0019 a0001c0001t0020g0241 a0002c0003t0005g0007 others(36): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-445G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081117 | |||||||
chr9:19081136 | G | A | 1 | a0001c0011t0004g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.871-464C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081136 | |||||||
chr9:19081196 | T | C | 1 | a0001c0004t0003g0304 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.871-524A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081196 | |||||||
chr9:19081223 | G | A | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.871-551C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081223 | |||||||
chr9:19081224 | T | C | 1 | a0001c0010t0002g0042 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.871-552A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081224 | |||||||
chr9:19081276 | G | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871-604C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081276 | |||||||
chr9:19081313 | T | A | 39 | a0001c0001t0001g0019 a0001c0001t0020g0241 a0002c0003t0005g0007 others(36): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.871-641A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081313 | |||||||
chr9:19081511 | C | T | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-839G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081511 | |||||||
chr9:19081622 | T | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.871-950A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081622 | |||||||
chr9:19081730 | T | C | 14 | a0001c0005t0003g0114 a0001c0005t0004g0098 a0001c0005t0004g0121 others(11): Show |
14 | HG01081.hp1 HG02572.hp2 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.871-1058A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081730 | |||||||
chr9:19081869 | G | A | 1 | a0001c0004t0003g0301 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.870+1004C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081869 | |||||||
chr9:19081899 | TACTAA | T | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.870+969_870+973del others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081899 | |||||||
chr9:19081922 | G | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.870+951C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081922 | |||||||
chr9:19081995 | G | C | 4 | a0001c0005t0008g0326 a0001c0005t0008g0327 a0001c0005t0008g0328 others(1): Show |
4 | HG02572.hp2 HG02970.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.870+878C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19081995 | |||||||
chr9:19082121 | T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.870+752A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082121 | |||||||
chr9:19082434 | GT | G | 58 | a0001c0005t0003g0114 a0001c0005t0004g0012 a0001c0005t0004g0098 others(55): Show |
61 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.870+438delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082434 | |||||||
chr9:19082434 | GTT | G | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+437_870+438del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082434 | |||||||
chr9:19082578 | G | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.870+295C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082578 | |||||||
chr9:19082639 | G | A | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.870+234C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082639 | |||||||
chr9:19082656 | G | A | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+217C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082656 | |||||||
chr9:19082678 | G | A | 1 | a0003c0006t0003g0148 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.870+195C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082678 | |||||||
chr9:19082743 | T | C | 38 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(35): Show |
41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.870+130A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082743 | |||||||
chr9:19082755 | AAAAAAAC | A | 78 | a0001c0002t0018g0171 a0001c0004t0003g0022 a0001c0004t0003g0023 others(75): Show |
82 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.870+111_870+117del others(7): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082755 | |||||||
chr9:19082834 | G | A | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.870+39C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 8/16 | chr9 | 19082834 | |||||||
chr9:19083057 | A | C | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.700-14T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083057 | |||||||
chr9:19083122 | T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.700-79A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083122 | |||||||
chr9:19083128 | C | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-85G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083128 | |||||||
chr9:19083277 | A | C | 1 | a0003c0006t0003g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700-234T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083277 | |||||||
chr9:19083449 | C | G | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.700-406G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083449 | |||||||
chr9:19083585 | G | A | 29 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(26): Show |
31 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.700-542C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083585 | |||||||
chr9:19083618 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.700-575G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083618 | |||||||
chr9:19083695 | G | A | 37 | a0001c0005t0023g0095 a0002c0003t0005g0007 a0002c0003t0005g0330 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.700-652C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083695 | |||||||
chr9:19083698 | A | G | 4 | a0001c0004t0003g0281 a0001c0004t0003g0282 a0001c0004t0003g0296 others(1): Show |
4 | HG03209.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.700-655T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083698 | |||||||
chr9:19083728 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0187 |
2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.700-685C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083728 | |||||||
chr9:19083733 | C | T | 21 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(18): Show |
23 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.700-690G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083733 | |||||||
chr9:19083756 | C | T | 7 | a0001c0007t0002g0141 a0001c0007t0002g0142 a0001c0007t0002g0143 others(4): Show |
7 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.700-713G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083756 | |||||||
chr9:19083757 | G | A | 1 | a0001c0004t0003g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.700-714C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083757 | |||||||
chr9:19083759 | G | A | 1 | a0003c0006t0003g0149 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.700-716C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083759 | |||||||
chr9:19083812 | A | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(107): Show |
122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.700-769T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083812 | |||||||
chr9:19083813 | A | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG04115.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.700-770T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083813 | |||||||
chr9:19083817 | AT | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.700-775delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083817 | |||||||
chr9:19083818 | T | A | 7 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0004t0003g0298 others(4): Show |
7 | HG02257.hp1 HG02258.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-775A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083818 | |||||||
chr9:19083852 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.700-809T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083852 | |||||||
chr9:19083943 | A | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.700-900T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083943 | |||||||
chr9:19083974 | C | T | 1 | a0001c0002t0002g0035 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.700-931G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083974 | |||||||
chr9:19083978 | C | T | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.700-935G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19083978 | |||||||
chr9:19084051 | C | CA | 134 | a0001c0002t0002g0033 a0001c0002t0002g0074 a0001c0002t0012g0031 others(131): Show |
141 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.700-1009dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084051 | |||||||
chr9:19084051 | C | CAA | 11 | a0001c0004t0003g0024 a0002c0003t0007g0338 a0003c0006t0003g0150 others(8): Show |
12 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.700-1010_700-1009d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084051 | |||||||
chr9:19084118 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.700-1075G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084118 | |||||||
chr9:19084177 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.700-1134T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084177 | |||||||
chr9:19084250 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.700-1207T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084250 | |||||||
chr9:19084345 | T | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.700-1302A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084345 | |||||||
chr9:19084407 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(111): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.700-1364C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084407 | |||||||
chr9:19084446 | T | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(158): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.700-1403A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084446 | |||||||
chr9:19084504 | T | C | 3 | a0001c0026t0028g0170 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.700-1461A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084504 | |||||||
chr9:19084531 | A | G | 37 | a0001c0005t0023g0095 a0002c0003t0005g0007 a0002c0003t0005g0330 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.700-1488T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084531 | |||||||
chr9:19084551 | G | C | 6 | a0001c0005t0004g0107 a0001c0005t0004g0113 a0001c0005t0004g0120 others(3): Show |
6 | HG03654.hp2 NA18990.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.700-1508C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084551 | |||||||
chr9:19084569 | T | TG | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.700-1527dupC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084569 | |||||||
chr9:19084582 | C | T | 1 | a0002c0003t0005g0351 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.700-1539G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084582 | |||||||
chr9:19084635 | CT | C | 72 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(69): Show |
77 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.700-1593delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084635 | |||||||
chr9:19084679 | C | A | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.700-1636G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084679 | |||||||
chr9:19084788 | A | G | 5 | a0001c0004t0003g0287 a0001c0004t0003g0288 a0001c0004t0003g0289 others(2): Show |
5 | HG00609.hp2 HG02135.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.700-1745T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084788 | |||||||
chr9:19084799 | CT | C | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.700-1757delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084799 | |||||||
chr9:19084958 | C | T | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.699+1776G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19084958 | |||||||
chr9:19085035 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.699+1699G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085035 | |||||||
chr9:19085442 | C | T | 1 | a0001c0001t0020g0241 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.699+1292G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085442 | |||||||
chr9:19085465 | T | C | 2 | a0002c0003t0005g0343 a0002c0003t0005g0350 |
2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.699+1269A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085465 | |||||||
chr9:19085466 | G | A | 3 | a0006c0014t0022g0124 a0006c0016t0014g0123 a0006c0016t0014g0125 |
3 | HG02109.hp2 HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.699+1268C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085466 | |||||||
chr9:19085615 | C | CA | 35 | a0001c0002t0002g0179 a0001c0004t0003g0106 a0001c0005t0003g0114 others(32): Show |
36 | HG01081.hp1 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.699+1118dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085615 | |||||||
chr9:19085615 | CA | C | 88 | a0001c0001t0001g0229 a0001c0002t0002g0036 a0001c0002t0002g0091 others(85): Show |
93 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.699+1118delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085615 | |||||||
chr9:19085908 | G | A | 1 | a0002c0030t0005g0321 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.699+826C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085908 | |||||||
chr9:19085991 | T | A | 1 | a0001c0002t0002g0070 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.699+743A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | |||||||
chr9:19085991 | T | TA | 47 | a0001c0001t0001g0262 a0001c0004t0003g0022 a0001c0004t0003g0023 others(44): Show |
50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.699+742dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | |||||||
chr9:19085991 | TA | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0174 a0001c0001t0001g0217 others(5): Show |
9 | HG01884.hp1 HG02717.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.699+742delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085991 | |||||||
chr9:19085992 | A | T | 2 | a0002c0003t0007g0333 a0003c0006t0003g0135 |
2 | HG00733.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.699+742T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19085992 | |||||||
chr9:19086034 | G | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0091 a0001c0005t0023g0095 |
3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.699+700C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086034 | |||||||
chr9:19086143 | C | T | 45 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(42): Show |
48 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.699+591G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086143 | |||||||
chr9:19086147 | A | G | 40 | a0001c0002t0002g0036 a0001c0002t0002g0091 a0001c0005t0023g0095 others(37): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.699+587T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086147 | |||||||
chr9:19086165 | G | C | 1 | a0001c0002t0002g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.699+569C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086165 | |||||||
chr9:19086188 | G | T | 1 | a0002c0003t0009g0313 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.699+546C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086188 | |||||||
chr9:19086288 | G | A | 3 | a0001c0002t0002g0076 a0001c0002t0002g0096 a0001c0002t0002g0097 |
3 | HG02056.hp2 NA18988.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.699+446C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086288 | |||||||
chr9:19086322 | G | A | 50 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(47): Show |
53 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.699+412C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086322 | |||||||
chr9:19086712 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.699+22G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 7/16 | chr9 | 19086712 | |||||||
chr9:19086787 | T | C | 1 | a0001c0002t0002g0085 | 1 | NA18991.hp2 | splice_region_variant&intron_variant | LOW | c.651-5A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086787 | |||||||
chr9:19086811 | C | T | 1 | a0003c0006t0003g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.651-29G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086811 | |||||||
chr9:19086870 | C | G | 1 | a0011c0018t0010g0102 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.651-88G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086870 | |||||||
chr9:19086968 | T | C | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.650+123A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086968 | |||||||
chr9:19086981 | C | T | 72 | a0001c0005t0003g0114 a0001c0005t0004g0012 a0001c0005t0004g0098 others(69): Show |
75 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.650+110G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 6/16 | chr9 | 19086981 | |||||||
chr9:19087198 | G | A | 37 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(34): Show |
40 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.585-42C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087198 | |||||||
chr9:19087205 | T | C | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-49A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087205 | |||||||
chr9:19087240 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.585-84A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087240 | |||||||
chr9:19087252 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.585-96C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087252 | |||||||
chr9:19087272 | G | A | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-116C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087272 | |||||||
chr9:19087273 | C | T | 2 | a0002c0003t0005g0343 a0002c0003t0005g0350 |
2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.585-117G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087273 | |||||||
chr9:19087373 | G | A | 1 | a0001c0035t0001g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.585-217C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087373 | |||||||
chr9:19087400 | G | A | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.585-244C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087400 | |||||||
chr9:19087431 | A | G | 92 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(89): Show |
97 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.585-275T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087431 | |||||||
chr9:19087597 | G | C | 2 | a0001c0007t0002g0143 a0001c0007t0002g0144 |
2 | HG01928.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.585-441C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087597 | |||||||
chr9:19087634 | G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.585-478C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087634 | |||||||
chr9:19087685 | C | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.585-529G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087685 | |||||||
chr9:19087755 | A | T | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.585-599T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087755 | |||||||
chr9:19087846 | C | CA | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(112): Show |
133 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.585-691dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | |||||||
chr9:19087846 | C | CAA | 22 | a0001c0001t0001g0019 a0001c0001t0001g0196 a0001c0001t0001g0207 others(19): Show |
23 | HG00597.hp1 HG00741.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.585-692_585-691dup others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | |||||||
chr9:19087846 | CA | C | 105 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0096 others(102): Show |
110 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.585-691delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087846 | |||||||
chr9:19087864 | A | G | 47 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(44): Show |
50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.585-708T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087864 | |||||||
chr9:19087895 | C | T | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.585-739G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087895 | |||||||
chr9:19087910 | G | C | 1 | a0005c0023t0001g0136 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.585-754C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19087910 | |||||||
chr9:19088014 | A | T | 2 | a0004c0008t0006g0362 a0004c0008t0006g0366 |
2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.585-858T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088014 | |||||||
chr9:19088034 | T | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.585-878A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088034 | |||||||
chr9:19088073 | G | C | 4 | a0006c0014t0010g0277 a0008c0017t0013g0172 a0008c0017t0013g0173 others(1): Show |
4 | HG01891.hp2 HG02055.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.585-917C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088073 | |||||||
chr9:19088098 | C | T | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.585-942G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088098 | |||||||
chr9:19088127 | T | C | 47 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(44): Show |
50 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.585-971A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088127 | |||||||
chr9:19088193 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.585-1037A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088193 | |||||||
chr9:19088308 | C | A | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.584+1104G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088308 | |||||||
chr9:19088377 | C | A | 4 | a0007c0013t0003g0294 a0007c0013t0011g0322 a0007c0013t0011g0323 others(1): Show |
4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+1035G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088377 | |||||||
chr9:19088409 | C | G | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.584+1003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088409 | |||||||
chr9:19088415 | C | CA | 71 | a0001c0001t0015g0215 a0001c0002t0002g0036 a0001c0002t0002g0048 others(68): Show |
75 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.584+996dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088415 | |||||||
chr9:19088588 | C | A | 26 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(23): Show |
28 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+824G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088588 | |||||||
chr9:19088713 | C | CA | 6 | a0001c0001t0001g0247 a0001c0001t0001g0261 a0001c0002t0002g0033 others(3): Show |
6 | HG01175.hp1 HG03017.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.584+698dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088713 | |||||||
chr9:19088740 | T | A | 4 | a0007c0013t0003g0294 a0007c0013t0011g0322 a0007c0013t0011g0323 others(1): Show |
4 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+672A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088740 | |||||||
chr9:19088773 | G | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.584+639C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088773 | |||||||
chr9:19088822 | G | A | 26 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(23): Show |
28 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.584+590C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088822 | |||||||
chr9:19088824 | G | GC | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.584+587dupG | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19088824 | |||||||
chr9:19089100 | G | C | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.584+312C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089100 | |||||||
chr9:19089198 | G | T | 1 | a0001c0004t0003g0283 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.584+214C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089198 | |||||||
chr9:19089222 | G | T | 37 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.584+190C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089222 | |||||||
chr9:19089267 | AAAG | A | 24 | a0001c0002t0002g0077 a0001c0007t0024g0162 a0001c0031t0002g0209 others(21): Show |
26 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.584+142_584+144del others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089267 | |||||||
chr9:19089277 | A | T | 1 | a0001c0002t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.584+135T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089277 | |||||||
chr9:19089295 | A | G | 46 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(43): Show |
49 | HG00099.hp2 HG00609.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.584+117T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089295 | |||||||
chr9:19089309 | G | A | 37 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.584+103C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089309 | |||||||
chr9:19089377 | A | C | 28 | a0001c0007t0024g0162 a0003c0006t0003g0013 a0003c0006t0003g0014 others(25): Show |
30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.584+35T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 5/16 | chr9 | 19089377 | |||||||
chr9:19089642 | A | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0091 a0001c0005t0023g0095 |
3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.437-83T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089642 | |||||||
chr9:19089645 | T | G | 37 | a0001c0005t0003g0114 a0001c0005t0004g0012 a0001c0005t0004g0098 others(34): Show |
38 | HG01081.hp1 HG01884.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.437-86A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089645 | |||||||
chr9:19089658 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.437-99T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089658 | |||||||
chr9:19089742 | A | G | 1 | a0001c0005t0003g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.437-183T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089742 | |||||||
chr9:19089749 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0275 |
2 | HG01099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.437-190C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089749 | |||||||
chr9:19089767 | C | T | 37 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.437-208G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089767 | |||||||
chr9:19089773 | T | A | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.437-214A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089773 | |||||||
chr9:19089856 | A | G | 1 | a0001c0005t0004g0121 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.437-297T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089856 | |||||||
chr9:19089877 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-318C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089877 | |||||||
chr9:19089961 | T | G | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-402A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19089961 | |||||||
chr9:19090233 | CAG | C | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-676_437-675del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090233 | |||||||
chr9:19090240 | T | C | 42 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0141 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.437-681A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090240 | |||||||
chr9:19090304 | G | C | 1 | a0003c0006t0003g0154 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.437-745C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090304 | |||||||
chr9:19090319 | G | A | 1 | a0003c0006t0003g0155 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.437-760C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090319 | |||||||
chr9:19090322 | A | G | 3 | a0002c0003t0005g0342 a0002c0003t0005g0349 a0002c0003t0005g0354 |
3 | NA18945.hp2 NA18953.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.437-763T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090322 | |||||||
chr9:19090388 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-829C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090388 | |||||||
chr9:19090416 | A | G | 168 | a0001c0001t0001g0257 a0001c0002t0002g0036 a0001c0002t0002g0091 others(165): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.437-857T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090416 | |||||||
chr9:19090423 | G | A | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.437-864C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090423 | |||||||
chr9:19090433 | C | T | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.437-874G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090433 | |||||||
chr9:19090457 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.437-898T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090457 | |||||||
chr9:19090538 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.437-979C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090538 | |||||||
chr9:19090580 | A | G | 1 | a0001c0004t0003g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.437-1021T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090580 | |||||||
chr9:19090674 | T | C | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.437-1115A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090674 | |||||||
chr9:19090755 | T | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.437-1196A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090755 | |||||||
chr9:19090898 | T | C | 6 | a0001c0001t0001g0203 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | NA18950.hp2 NA18960.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-1339A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090898 | |||||||
chr9:19090957 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.437-1398G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090957 | |||||||
chr9:19090973 | T | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.437-1414A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19090973 | |||||||
chr9:19091072 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.437-1513C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091072 | |||||||
chr9:19091107 | T | C | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-1548A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091107 | |||||||
chr9:19091113 | A | T | 3 | a0001c0002t0002g0036 a0001c0002t0002g0091 a0001c0005t0023g0095 |
3 | HG03017.hp2 HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.437-1554T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091113 | |||||||
chr9:19091255 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.437-1696C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091255 | |||||||
chr9:19091259 | C | T | 40 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(37): Show |
43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.437-1700G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091259 | |||||||
chr9:19091277 | G | C | 1 | a0001c0007t0002g0156 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.437-1718C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091277 | |||||||
chr9:19091287 | G | A | 1 | a0001c0004t0003g0105 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.437-1728C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091287 | |||||||
chr9:19091294 | C | T | 1 | a0001c0002t0002g0057 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.437-1735G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091294 | |||||||
chr9:19091296 | T | A | 1 | a0001c0002t0002g0049 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.437-1737A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091296 | |||||||
chr9:19091301 | G | GA | 6 | a0001c0002t0012g0031 a0001c0004t0003g0306 a0001c0004t0003g0309 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1743dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091301 | |||||||
chr9:19091301 | GA | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
121 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.437-1743delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091301 | |||||||
chr9:19091318 | A | G | 5 | a0001c0005t0004g0133 a0001c0005t0008g0326 a0001c0005t0008g0327 others(2): Show |
5 | HG02572.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.437-1759T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091318 | |||||||
chr9:19091375 | C | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+1796G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091375 | |||||||
chr9:19091389 | C | T | 91 | a0001c0002t0002g0036 a0001c0002t0002g0091 a0001c0002t0018g0171 others(88): Show |
96 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.436+1782G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091389 | |||||||
chr9:19091488 | T | C | 5 | a0001c0004t0003g0282 a0007c0013t0003g0294 a0007c0013t0011g0322 others(2): Show |
5 | HG01243.hp2 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+1683A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091488 | |||||||
chr9:19091573 | G | C | 1 | a0003c0006t0003g0157 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.436+1598C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091573 | |||||||
chr9:19091587 | G | A | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.436+1584C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091587 | |||||||
chr9:19091628 | T | A | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+1543A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091628 | |||||||
chr9:19091634 | A | G | 40 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(37): Show |
43 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.436+1537T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091634 | |||||||
chr9:19091767 | T | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.436+1404A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091767 | |||||||
chr9:19091807 | G | A | 2 | a0001c0005t0004g0107 a0001c0005t0004g0134 |
2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.436+1364C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091807 | |||||||
chr9:19091973 | A | AT | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+1197dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091973 | |||||||
chr9:19091975 | T | A | 2 | a0001c0005t0004g0117 a0001c0005t0004g0118 |
2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.436+1196A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19091975 | |||||||
chr9:19092032 | A | G | 45 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(42): Show |
47 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.436+1139T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092032 | |||||||
chr9:19092110 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0273 |
3 | NA18973.hp1 NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.436+1061G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092110 | |||||||
chr9:19092192 | T | C | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+979A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092192 | |||||||
chr9:19092291 | T | TA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.436+879dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092291 | |||||||
chr9:19092298 | A | C | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.436+873T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092298 | |||||||
chr9:19092301 | A | C | 88 | a0001c0004t0003g0296 a0001c0007t0002g0137 a0001c0007t0002g0139 others(85): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.436+870T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092301 | |||||||
chr9:19092303 | A | C | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+868T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092303 | |||||||
chr9:19092378 | G | C | 1 | a0002c0003t0032g0353 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.436+793C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092378 | |||||||
chr9:19092405 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | NA18950.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.436+766G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092405 | |||||||
chr9:19092406 | G | A | 1 | a0003c0006t0003g0160 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.436+765C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092406 | |||||||
chr9:19092434 | G | A | 4 | a0001c0005t0003g0114 a0001c0005t0004g0098 a0001c0005t0004g0121 others(1): Show |
4 | HG02602.hp1 HG02683.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+737C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092434 | |||||||
chr9:19092472 | G | A | 1 | a0002c0003t0005g0348 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.436+699C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092472 | |||||||
chr9:19092597 | A | G | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+574T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092597 | |||||||
chr9:19092598 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436+573T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092598 | |||||||
chr9:19092616 | C | CG | 16 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0015g0215 others(13): Show |
17 | HG01884.hp2 HG02109.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.436+554dupC | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092616 | |||||||
chr9:19092618 | G | GA | 56 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0197 others(53): Show |
56 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.436+552dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | |||||||
chr9:19092618 | G | GGA | 5 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0005t0004g0115 others(2): Show |
5 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+552_436+553ins others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | |||||||
chr9:19092618 | GA | G | 7 | a0001c0001t0001g0193 a0001c0001t0001g0211 a0001c0001t0001g0212 others(4): Show |
7 | HG01891.hp2 HG01928.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+552delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | |||||||
chr9:19092618 | GAAAA | G | 33 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(30): Show |
35 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.436+549_436+552del others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | |||||||
chr9:19092618 | GAAAAA | G | 8 | a0002c0003t0005g0341 a0004c0008t0006g0025 a0004c0008t0006g0362 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+548_436+552del others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092618 | |||||||
chr9:19092623 | A | G | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.436+548T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092623 | |||||||
chr9:19092644 | C | G | 1 | a0019c0040t0004g0316 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.436+527G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092644 | |||||||
chr9:19092649 | C | T | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+522G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092649 | |||||||
chr9:19092650 | G | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0198 |
3 | HG00735.hp1 HG01433.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.436+521C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092650 | |||||||
chr9:19092703 | A | C | 40 | a0001c0002t0018g0171 a0002c0003t0005g0007 a0002c0003t0005g0330 others(37): Show |
42 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.436+468T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092703 | |||||||
chr9:19092788 | G | C | 1 | a0001c0007t0002g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.436+383C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092788 | |||||||
chr9:19092795 | G | C | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.436+376C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092795 | |||||||
chr9:19092803 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436+368A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092803 | |||||||
chr9:19092862 | T | C | 3 | a0004c0008t0006g0025 a0004c0008t0006g0364 a0004c0008t0006g0367 |
3 | HG00099.hp2 HG02486.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.436+309A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092862 | |||||||
chr9:19092886 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0204 a0001c0001t0001g0210 others(4): Show |
8 | HG01167.hp1 HG01361.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.436+285A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092886 | |||||||
chr9:19092916 | C | CA | 48 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0190 others(45): Show |
51 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.436+254dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(6): Show |
1 | a0002c0003t0005g0360 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.436+242_436+254dup others(13): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(7): Show |
1 | a0020c0028t0005g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.436+241_436+254dup others(14): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(8): Show |
18 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0339 others(15): Show |
20 | HG00140.hp2 HG00639.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.436+240_436+254dup others(15): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(9): Show |
9 | a0002c0003t0005g0331 a0002c0003t0005g0332 a0002c0003t0005g0349 others(6): Show |
9 | HG00741.hp2 HG02015.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+239_436+254dup others(16): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(10): Show |
6 | a0002c0003t0005g0355 a0002c0003t0005g0356 a0002c0003t0007g0335 others(3): Show |
6 | HG00733.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+238_436+254dup others(17): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092916 | C | CAAAAAAA others(11): Show |
2 | a0002c0003t0007g0333 a0002c0003t0007g0338 |
2 | HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.436+254_436+255ins others(18): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092916 | |||||||
chr9:19092983 | G | C | 2 | a0001c0005t0004g0107 a0001c0005t0004g0134 |
2 | NA19009.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.436+188C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19092983 | |||||||
chr9:19093019 | C | G | 88 | a0001c0002t0018g0171 a0001c0007t0002g0137 a0001c0007t0002g0139 others(85): Show |
92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.436+152G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093019 | |||||||
chr9:19093050 | G | C | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.436+121C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093050 | |||||||
chr9:19093051 | G | A | 1 | a0001c0012t0004g0127 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436+120C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093051 | |||||||
chr9:19093100 | G | A | 43 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(40): Show |
45 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.436+71C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093100 | |||||||
chr9:19093120 | C | A | 5 | a0001c0004t0003g0306 a0001c0004t0003g0309 a0010c0021t0003g0293 others(2): Show |
5 | HG02451.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+51G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 4/16 | chr9 | 19093120 | |||||||
chr9:19093343 | A | G | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.304-40T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093343 | |||||||
chr9:19093414 | C | T | 2 | a0001c0002t0002g0181 a0001c0002t0002g0182 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.304-111G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093414 | |||||||
chr9:19093528 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-225C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093528 | |||||||
chr9:19093651 | T | A | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.304-348A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093651 | |||||||
chr9:19093740 | A | C | 1 | a0022c0025t0002g0056 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.304-437T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093740 | |||||||
chr9:19093763 | G | T | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.304-460C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093763 | |||||||
chr9:19093787 | C | T | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-484G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093787 | |||||||
chr9:19093791 | C | G | 1 | a0002c0003t0007g0333 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.304-488G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093791 | |||||||
chr9:19093833 | C | G | 37 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(34): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.303+484G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093833 | |||||||
chr9:19093960 | A | G | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+357T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19093960 | |||||||
chr9:19094217 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+100C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19094217 | |||||||
chr9:19094283 | A | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.303+34T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 3/16 | chr9 | 19094283 | |||||||
chr9:19094424 | C | G | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.225-29G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094424 | |||||||
chr9:19094434 | C | T | 1 | a0001c0005t0004g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.225-39G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094434 | |||||||
chr9:19094516 | G | A | 1 | a0004c0008t0006g0365 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.225-121C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094516 | |||||||
chr9:19094519 | C | T | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-124G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094519 | |||||||
chr9:19094520 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.225-125C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094520 | |||||||
chr9:19094621 | G | A | 39 | a0001c0002t0002g0279 a0001c0002t0002g0280 a0002c0003t0005g0007 others(36): Show |
41 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.225-226C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094621 | |||||||
chr9:19094638 | A | G | 1 | a0009c0015t0003g0284 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.225-243T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094638 | |||||||
chr9:19094752 | C | G | 3 | a0001c0026t0028g0170 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.225-357G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094752 | |||||||
chr9:19094800 | A | G | 3 | a0001c0001t0001g0186 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00323.hp2 HG02300.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.225-405T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19094800 | |||||||
chr9:19095058 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.225-663A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095058 | |||||||
chr9:19095086 | C | T | 9 | a0001c0004t0003g0104 a0001c0004t0003g0105 a0001c0004t0003g0287 others(6): Show |
9 | HG00609.hp2 HG02135.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.225-691G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095086 | |||||||
chr9:19095112 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.225-717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095112 | |||||||
chr9:19095119 | C | A | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.225-724G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095119 | |||||||
chr9:19095146 | T | C | 1 | a0001c0024t0021g0177 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225-751A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095146 | |||||||
chr9:19095161 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-766C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095161 | |||||||
chr9:19095210 | G | C | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-815C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095210 | |||||||
chr9:19095235 | T | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-840A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095235 | |||||||
chr9:19095273 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.225-878T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095273 | |||||||
chr9:19095312 | T | C | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-917A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095312 | |||||||
chr9:19095313 | T | G | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-918A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095313 | |||||||
chr9:19095365 | G | A | 38 | a0002c0003t0005g0007 a0002c0003t0005g0330 a0002c0003t0005g0331 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.225-970C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095365 | |||||||
chr9:19095504 | C | CA | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
163 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.225-1110dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095504 | |||||||
chr9:19095504 | CA | C | 11 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(8): Show |
11 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-1110delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095504 | |||||||
chr9:19095565 | A | G | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+1109T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095565 | |||||||
chr9:19095682 | T | C | 1 | a0001c0002t0012g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.224+992A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095682 | |||||||
chr9:19095754 | T | C | 1 | a0004c0008t0030g0320 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224+920A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095754 | |||||||
chr9:19095851 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.224+823A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095851 | |||||||
chr9:19095881 | G | A | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.224+793C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095881 | |||||||
chr9:19095994 | C | T | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.224+680G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19095994 | |||||||
chr9:19096042 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.224+632C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096042 | |||||||
chr9:19096066 | C | T | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.224+608G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096066 | |||||||
chr9:19096070 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.224+604T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096070 | |||||||
chr9:19096442 | A | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.224+232T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096442 | |||||||
chr9:19096458 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.224+216T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096458 | |||||||
chr9:19096552 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.224+122C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096552 | |||||||
chr9:19096564 | C | CA | 15 | a0001c0002t0002g0050 a0001c0002t0002g0054 a0001c0002t0002g0076 others(12): Show |
15 | HG00140.hp1 HG00423.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.224+109dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | C | CAAA | 33 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(30): Show |
36 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.224+107_224+109dup others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | C | CAAAAA | 20 | a0001c0004t0003g0106 a0001c0005t0003g0114 a0001c0005t0004g0012 others(17): Show |
21 | HG01884.hp2 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.224+105_224+109dup others(5): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | C | CAAAAAA | 10 | a0001c0005t0004g0098 a0001c0005t0004g0116 a0001c0005t0004g0117 others(7): Show |
10 | HG02602.hp1 HG02818.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.224+104_224+109dup others(6): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | CA | C | 16 | a0001c0001t0001g0178 a0001c0002t0002g0078 a0001c0002t0012g0031 others(13): Show |
16 | HG00423.hp2 HG00544.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.224+109delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | CAA | C | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | NA18951.hp2 NA18985.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+108_224+109del others(2): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | CAAA | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
116 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.224+107_224+109del others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | CAAAA | C | 9 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0272 others(6): Show |
9 | HG00099.hp2 HG00323.hp2 HG01069.hp2 others(6): Show |
intron_variant | MODIFIER | c.224+106_224+109del others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096564 | CAAAAAAA others(6): Show |
C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.224+97_224+109delT others(12): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096564 | |||||||
chr9:19096578 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.224+96T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096578 | |||||||
chr9:19096598 | T | C | 14 | a0001c0002t0002g0003 a0001c0002t0002g0004 a0001c0002t0002g0078 others(11): Show |
19 | HG00597.hp2 HG00621.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.224+76A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096598 | |||||||
chr9:19096646 | T | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.224+28A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 2/16 | chr9 | 19096646 | |||||||
chr9:19096816 | A | G | 1 | a0001c0004t0003g0022 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.129-47T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096816 | |||||||
chr9:19096834 | A | T | 42 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.129-65T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096834 | |||||||
chr9:19096956 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.129-187G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096956 | |||||||
chr9:19096981 | A | G | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-212T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096981 | |||||||
chr9:19096997 | T | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0269 |
3 | NA18957.hp2 NA18969.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.129-228A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096997 | |||||||
chr9:19096998 | G | A | 4 | a0001c0011t0004g0128 a0001c0011t0004g0129 a0001c0011t0004g0130 others(1): Show |
4 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-229C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19096998 | |||||||
chr9:19097025 | A | C | 3 | a0001c0026t0028g0170 a0011c0018t0010g0102 a0011c0018t0010g0103 |
3 | HG02258.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.129-256T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097025 | |||||||
chr9:19097035 | A | T | 1 | a0001c0002t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.129-266T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097035 | |||||||
chr9:19097117 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129-348C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097117 | |||||||
chr9:19097124 | T | A | 1 | a0006c0014t0022g0124 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.129-355A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097124 | |||||||
chr9:19097153 | G | A | 1 | a0003c0006t0027g0164 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.129-384C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097153 | |||||||
chr9:19097166 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0205 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.129-397T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097166 | |||||||
chr9:19097235 | C | A | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129-466G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097235 | |||||||
chr9:19097252 | G | C | 1 | a0011c0018t0010g0103 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.129-483C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097252 | |||||||
chr9:19097320 | G | A | 161 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(158): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.129-551C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097320 | |||||||
chr9:19097355 | C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129-586G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097355 | |||||||
chr9:19097379 | A | C | 45 | a0001c0007t0002g0137 a0001c0007t0002g0139 a0001c0007t0002g0140 others(42): Show |
47 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.129-610T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097379 | |||||||
chr9:19097398 | T | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-629A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097398 | |||||||
chr9:19097464 | G | A | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.129-695C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097464 | |||||||
chr9:19097489 | A | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0026 a0001c0002t0002g0052 others(7): Show |
11 | HG02015.hp1 HG03831.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-720T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097489 | |||||||
chr9:19097506 | T | C | 1 | a0001c0002t0002g0090 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.129-737A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097506 | |||||||
chr9:19097576 | G | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(281): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.129-807C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097576 | |||||||
chr9:19097767 | T | TA | 42 | a0001c0005t0004g0121 a0001c0005t0004g0122 a0001c0007t0002g0137 others(39): Show |
44 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.129-999dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097767 | |||||||
chr9:19097775 | A | C | 39 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(36): Show |
42 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(39): Show |
intron_variant | MODIFIER | c.129-1006T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097775 | |||||||
chr9:19097780 | A | AT | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-1012_129-1011i others(3): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097780 | |||||||
chr9:19097953 | T | C | 5 | a0001c0004t0003g0287 a0001c0004t0003g0288 a0001c0004t0003g0289 others(2): Show |
5 | HG00609.hp2 HG02135.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-1184A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19097953 | |||||||
chr9:19098111 | G | A | 1 | a0003c0006t0003g0165 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.129-1342C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098111 | |||||||
chr9:19098162 | C | T | 1 | a0001c0005t0004g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.129-1393G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098162 | |||||||
chr9:19098165 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.129-1396C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098165 | |||||||
chr9:19098221 | A | G | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129-1452T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098221 | |||||||
chr9:19098259 | G | A | 1 | a0001c0005t0023g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.129-1490C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098259 | |||||||
chr9:19098267 | A | G | 163 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(160): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.129-1498T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098267 | |||||||
chr9:19098357 | G | A | 2 | a0002c0003t0005g0330 a0002c0003t0005g0331 |
2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-1588C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098357 | |||||||
chr9:19098401 | G | A | 38 | a0001c0037t0001g0311 a0002c0003t0005g0007 a0002c0003t0005g0330 others(35): Show |
40 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.129-1632C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098401 | |||||||
chr9:19098436 | C | CA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(103): Show |
118 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.129-1668dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | |||||||
chr9:19098436 | C | CAA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
9 | HG00544.hp1 HG00609.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.129-1669_129-1668d others(4): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | |||||||
chr9:19098436 | CA | C | 110 | a0001c0002t0002g0181 a0001c0002t0002g0182 a0001c0004t0003g0022 others(107): Show |
116 | HG00140.hp2 HG00609.hp2 HG00733.hp2 others(113): Show |
intron_variant | MODIFIER | c.129-1668delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098436 | |||||||
chr9:19098470 | A | T | 16 | a0001c0002t0002g0030 a0001c0002t0002g0037 a0001c0002t0002g0038 others(13): Show |
17 | HG00423.hp1 HG02523.hp2 NA18950.hp1 others(14): Show |
intron_variant | MODIFIER | c.129-1701T>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098470 | |||||||
chr9:19098478 | C | G | 8 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.129-1709G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098478 | |||||||
chr9:19098507 | C | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-1738G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098507 | |||||||
chr9:19098508 | C | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-1739G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098508 | |||||||
chr9:19098613 | G | C | 1 | a0001c0005t0004g0133 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.129-1844C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098613 | |||||||
chr9:19098642 | A | C | 1 | a0012c0042t0016g0318 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129-1873T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098642 | |||||||
chr9:19098649 | C | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.129-1880G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098649 | |||||||
chr9:19098714 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(278): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.129-1945T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098714 | |||||||
chr9:19098729 | T | TA | 274 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(271): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.129-1961dupT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098729 | |||||||
chr9:19098772 | C | G | 8 | a0001c0037t0001g0311 a0002c0003t0007g0333 a0002c0003t0007g0334 others(5): Show |
8 | HG02818.hp1 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-2003G>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098772 | |||||||
chr9:19098947 | GGGAGGC | G | 38 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(35): Show |
41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.129-2184_129-2179d others(8): Show |
HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098947 | |||||||
chr9:19098957 | G | C | 2 | a0001c0002t0002g0181 a0001c0002t0002g0182 |
2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.129-2188C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098957 | |||||||
chr9:19098969 | G | A | 124 | a0001c0004t0003g0022 a0001c0004t0003g0023 a0001c0004t0003g0024 others(121): Show |
130 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.129-2200C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19098969 | |||||||
chr9:19099017 | CA | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.129-2249delT | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099017 | |||||||
chr9:19099052 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.129-2283A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099052 | |||||||
chr9:19099065 | G | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0184 a0001c0001t0001g0185 others(13): Show |
17 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.129-2296C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099065 | |||||||
chr9:19099067 | G | T | 1 | a0001c0002t0002g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.129-2298C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099067 | |||||||
chr9:19099090 | A | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129-2321T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099090 | |||||||
chr9:19099144 | T | C | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.129-2375A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099144 | |||||||
chr9:19099171 | G | GT | 10 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0032 others(7): Show |
10 | HG02258.hp1 HG03453.hp1 HG03540.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-2403dupA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099171 | |||||||
chr9:19099171 | GT | G | 66 | a0001c0004t0003g0024 a0001c0004t0003g0281 a0001c0004t0003g0282 others(63): Show |
69 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.129-2403delA | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099171 | |||||||
chr9:19099225 | G | A | 2 | a0002c0003t0005g0330 a0002c0003t0005g0331 |
2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.129-2456C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099225 | |||||||
chr9:19099226 | G | C | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-2457C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099226 | |||||||
chr9:19099228 | G | A | 1 | a0006c0016t0014g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.129-2459C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099228 | |||||||
chr9:19099244 | G | T | 4 | a0001c0012t0004g0099 a0001c0012t0004g0100 a0001c0012t0004g0101 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-2475C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099244 | |||||||
chr9:19099461 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
132 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.129-2692G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099461 | |||||||
chr9:19099503 | T | A | 1 | a0001c0004t0003g0310 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129-2734A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099503 | |||||||
chr9:19099560 | G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.129-2791C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099560 | |||||||
chr9:19099653 | G | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+2871C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099653 | |||||||
chr9:19099764 | C | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+2760G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099764 | |||||||
chr9:19099774 | G | C | 1 | a0003c0006t0003g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128+2750C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099774 | |||||||
chr9:19099807 | T | C | 1 | a0001c0012t0004g0127 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.128+2717A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099807 | |||||||
chr9:19099807 | T | G | 1 | a0006c0014t0025g0126 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.128+2717A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099807 | |||||||
chr9:19099820 | C | T | 1 | a0001c0005t0004g0098 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.128+2704G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099820 | |||||||
chr9:19099821 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
124 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.128+2703C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099821 | |||||||
chr9:19099968 | T | A | 7 | a0004c0008t0006g0025 a0004c0008t0006g0362 a0004c0008t0006g0363 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+2556A>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19099968 | |||||||
chr9:19100020 | C | T | 36 | a0002c0003t0005g0007 a0002c0003t0005g0332 a0002c0003t0005g0339 others(33): Show |
38 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.128+2504G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100020 | |||||||
chr9:19100062 | G | A | 6 | a0001c0005t0004g0132 a0001c0005t0004g0133 a0001c0005t0008g0326 others(3): Show |
6 | HG01081.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+2462C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100062 | |||||||
chr9:19100098 | G | A | 1 | a0002c0003t0007g0368 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.128+2426C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100098 | |||||||
chr9:19100254 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18953.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.128+2270G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100254 | |||||||
chr9:19100307 | A | C | 2 | a0008c0017t0013g0172 a0008c0017t0013g0173 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.128+2217T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100307 | |||||||
chr9:19100485 | G | C | 1 | a0001c0037t0001g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.128+2039C>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100485 | |||||||
chr9:19100519 | T | C | 2 | a0001c0005t0023g0095 a0001c0007t0002g0168 |
2 | HG00423.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.128+2005A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100519 | |||||||
chr9:19100547 | G | A | 1 | a0001c0005t0004g0134 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.128+1977C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100547 | |||||||
chr9:19100901 | G | A | 1 | a0018c0022t0026g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.128+1623C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19100901 | |||||||
chr9:19101040 | A | G | 1 | a0003c0006t0003g0135 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.128+1484T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101040 | |||||||
chr9:19101051 | T | C | 41 | a0001c0002t0002g0028 a0001c0002t0018g0171 a0001c0007t0002g0137 others(38): Show |
43 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.128+1473A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101051 | |||||||
chr9:19101082 | A | C | 1 | a0001c0019t0001g0029 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.128+1442T>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101082 | |||||||
chr9:19101087 | C | T | 2 | a0001c0004t0003g0281 a0001c0004t0003g0282 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.128+1437G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101087 | |||||||
chr9:19101223 | G | A | 1 | a0001c0026t0028g0170 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.128+1301C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101223 | |||||||
chr9:19101342 | G | T | 1 | a0001c0002t0018g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128+1182C>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101342 | |||||||
chr9:19101352 | A | G | 121 | a0001c0002t0002g0028 a0001c0004t0003g0022 a0001c0004t0003g0023 others(118): Show |
127 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.128+1172T>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101352 | |||||||
chr9:19101368 | G | A | 1 | a0023c0041t0001g0317 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.128+1156C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101368 | |||||||
chr9:19101449 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128+1075G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101449 | |||||||
chr9:19101574 | T | C | 2 | a0001c0002t0002g0096 a0001c0002t0002g0097 |
2 | NA18988.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.128+950A>G | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101574 | |||||||
chr9:19101660 | G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128+864C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101660 | |||||||
chr9:19101718 | G | A | 2 | a0001c0002t0002g0279 a0001c0002t0002g0280 |
2 | NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.128+806C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101718 | |||||||
chr9:19101773 | G | A | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.128+751C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101773 | |||||||
chr9:19101896 | G | A | 1 | a0006c0014t0010g0277 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.128+628C>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101896 | |||||||
chr9:19101912 | C | A | 3 | a0001c0002t0002g0278 a0001c0002t0002g0279 a0001c0002t0002g0280 |
3 | HG02015.hp1 NA18942.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.128+612G>T | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101912 | |||||||
chr9:19101932 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.128+592G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19101932 | |||||||
chr9:19102202 | AC | A | 38 | a0001c0001t0001g0312 a0001c0004t0003g0022 a0001c0004t0003g0023 others(35): Show |
41 | HG00609.hp2 HG01123.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.128+321delG | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102202 | |||||||
chr9:19102234 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.128+290G>A | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102234 | |||||||
chr9:19102345 | T | G | 50 | a0001c0002t0031g0325 a0001c0005t0008g0326 a0001c0005t0008g0327 others(47): Show |
52 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.128+179A>C | HAUS6 | ENSG00000147874.11 | transcript | ENST00000380502.8 | protein_coding | 1/16 | chr9 | 19102345 |